The paecilin puzzle - Enantioselective syntheses of the proposed structures of paecilin A and B

Article abstract of DOI:10.3987/COM-13-S(S)68

For the synthesis of the two diastereomers 3c and 3d of the proposed structure of paecilin B (3) phenol 19, containing an alkenyl moiety, was treated with Pd(II) in the presence of the chiral BOXAX ligand 9b to give 20 with 96% ee. A subsequent Sharpless dihydroxylation afforded two isomeric diols, which were further transformed into 31 and 32. The final steps included removal of the silyl protecting group with simultaneous lactone formation, oxidation and cleavage of the methyl ether. For the preparation of the dimeric paecilin A (1) brominated intermediate 38 was treated with (Bpin)2, S-Phos and Pd(OAc)2. The spectroscopic data of the new compounds did not match those of the isolated natural products.

Full text of DOI:10.3987/COM-13-S(S)68

HETEROCYCLES, Vol. 88, No. 2, 2014
1101
HETEROCYCLES, Vol. 88, No. 2, 2014, pp. 1101 - 1119. © 2014 The Japan Institute of Heterocyclic Chemistry
Received, 29th June, 2013, Accepted, 31st July, 2013, Published online, 8th August, 2013
DOI: 10.3987/COM-13-S(S)68
THE PAECILIN PUZZLE –
ENANTIOSELECTIVE SYNTHESES OF THE
PROPOSED STRUCTURES OF PAECILIN AAND B
Lutz F. Tietze,* Ling Ma, Stefan Jackenkroll, Johannes R. Reiner, Judith
Hierold, Boopathy Gnanaprakasam, and Sven Heidemann
Institute of Organic and Biomolecular Chemistry, Georg-August-Universität
Göttingen, Tammannstr. 2, 37077 Göttingen, Germany
ltietze@gwdg.de
Dedicated to Professor Dr. Victor Snieckus on the occasion of his 77th birthday
Abstract – For the synthesis of the two diastereomers 3c and 3d of the proposed
structure of paecilin B (3) phenol 19, containing an alkenyl moiety, was treated with
Pd(II) in the presence of the chiral BOXAX ligand 9b to give 20 with 96% ee. A
subsequent Sharpless dihydroxylation afforded two isomeric diols, which were
further transformed into 31 and 32. The final steps included removal of the silyl
protecting group with simultaneous lactone formation, oxidation and cleavage of
the methyl ether. For the preparation of the dimeric paecilin A (1) brominated
intermediate 38 was treated with (Bpin)2, S-Phos and Pd(OAc)2. The spectroscopic
data of the new compounds did not match those of the isolated natural products.
INTRODUCTION
The secondary metabolites paecilin A (1) and B (3) of the endophytic fungus Paecilomyces sp. have been
isolated in 2007 by Guo et al.; however, the authors only published the constitution of these natural
products, the absolute and relative configurations are still unknown.1 Both paecilins have a chromanone
skeleton and contain quaternary stereogenic centers as well as γ-lactone moieties. Paecilin A (1) is likely a
dimer of paecilin B (3) with a 8,8’-biaryl connection. In an initial bioassay, paecilin A (1) and B (3) were
tested using KB cell lines, but showed no pronounced cytotoxicity. However, several structurally related
chromanones substituted with a γ-lactone moiety exhibit promising biological activities such as the dimer
gonytolide A (2), which promotes the innate immune response.2 Therefore, it seems reasonable to assume
that 1 and 3 may also have some so far unknown bioactivities.

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Figure 1. Paecilin A (1) and B (3), gonytolide A (2), diversonol (4) and blennolide A and B (5)
Paecilin B (3) contains three stereogenic centers, therefore it could exist in eight different stereoisomeric
forms, the diastereomers 3a-d and their enantiomers ent-3a-d (Figure 2). Though the absolute
configuration of 3 is not known, a comparison with the natural products gonytolide A (2),2 diversonol (4)4
as well as blennolide A (5a) and blennolide B (5b)3 would make it feasible to assume that paecilin B should
have the relative and absolute configuration as depicted in 3a-d. Recently, Porco et al. described a very nice
synthesis of the two racemic diastereomers 3a and 3b; however, their spectroscopic data did not match
those published for 3.3c They therefore concluded that the natural product must be 3c, 3d or their respective
enantiomers.
Figure 2. Possible diastereomers of paecilin B (3a-d)

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Recently, we have described the total syntheses of the tetrahydroxanthenones (–)-diversonol (ent-4)4c and
(–)-blennolide A (ent-5a).3b For the synthesis of (–)-diversonol (ent-4) we employed an enantioselective
domino Wacker/carbonylation/methoxylation reaction using BOXAX ligand 9a to furnish ester 7 in 96% ee
and 80% yield (Scheme 1).4c,5
A: Enantioselective domino Wacker/carbonylation/methoxylation
OMe
OMe
O
N
O
Bn
Bn
N
O
O
R
OH
6
7: R = OMe
8: R = H
9a
B: Proposed pathway for the racemization
C: Sharpless dihydroxylation
Scheme 1. Enantioselective total synthesis of (–)-diversonol (ent-4)

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Reduction of 7 to form aldehyde 8 set the stage for the direct introduction of the hydroxyl group at C-4
(numbering as in 4) using a hydroxylating Knoevenagel condensation.6 To our surprise, however, the steric
integrity of the stereogenic center in 8 was lost in the course of the reaction to yield the racemic esters
rac-11 and rac-12. Most likely, a retro-1,6-Michael addition led to an opening of the chroman ring system
and subsequent racemization via the intermediates 13-16. We therefore sought alternative ways for the
hydroxylation. In a revised strategy we introduced the C-4 hydroxy group via a Sharpless dihydroxylation7
of readily accessible vinyl chroman 17, which led to ent-4 after 10 additional steps.
In a related approach we synthesized (–)-blennolide A (ent-5a) via an enantioselective domino
Wacker/carbonylation/methoxylation reaction with 96% ee as described before and an enantioselective
Wacker oxidation of the diastereomeric alkenyl phenols 19 (E/Z = 1:1.7) to give vinyl chroman 20 using
catalytic amounts of palladium(II) trifluoracetate [Pd(OTFA)2] and the chiral (S,S)-Bn-BOXAX ligand 9a
in methanol with however only 85% ee and 82% yield (Scheme 2).3b
Scheme 2. Enantioselective total synthesis of (–)-blennolide A (ent-5a)
Herein we report the syntheses of two diastereomers of the proposed structures of paecilin B (3) in their
enantiomeric forms ent-3c and ent-3d and one diastereomer of the dimer paecilin A (1) using an
enantioselective Wacker oxidation to finally solve the absolute and relative configuration of paecilin A (1)
and paecilin B (3) and moreover to provide enough material for further biological studies.
RESULTS AND DISCUSSION
In accordance with the syntheses of ent-4 and ent-5a, retrosynthetic analysis of the dimer paecilin A (1)
leads to the methylated monomeric paecilin B (22) via halogenated intermediate 21, from which 1 could be
obtained via a Suzuki type coupling. Methylated paecilin B (22) should be accessible from 23 by benzylic
oxidation and lactonization (Scheme 3). The latter could arise from intermediate 20, employing a
dihydroxylation and Wittig-Horner reaction followed by Michael addition.

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Scheme 3. Retrosynthetic analysis of paecilin A (1)
Finally, for the synthesis of 20 an enantioselective Wacker oxidation of 19 was envisaged, which in turn can
be synthesized from resorcinol (24) in six steps.
As already mentioned, an enantioselective Wacker oxidation of 19 to give 20 has been used by us for the
synthesis of (-)-blennolide A (ent-5a)3b using the chiral (S,S)-Bn-BOXAX ligand (9a)8 in methanol with
85% ee and 82% yield. Gratifyingly, the enantioselective Wacker oxidation of 19 could now be improved
using (S,S)-iPr-BOXAX (9b) instead of 9a, which resulted in an enantioselectivity of 96% ee and an almost
identical yield of 79% (Scheme 4).
Scheme 4. Synthesis of 20: a) 10 mol% [Pd(OTFA)2], 10 mol% BOXAX ligand (9a and 9b),
p-benzoquinone, MeOH, 60 °C, 24 h, E/Z-19 (E/Z = 1:1.7), for (S,S)-Bn-BOXAX (9a): 82%, 85% ee; for
(S,S)-iPr-BOXAX (9b): 79%, 96% ee
Sharpless dihydroxylation of 20 in which the desired hydroxyl groups at C-1’and C-2’(numbering as in 20)
were set up, was followed by a sequence of double TBS protection, chemoselective removal of the primary

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silyl group and subsequent oxidation to give the aldehydes 25 and 26, which could be readily separated by
column chromatography (Scheme 5). In analogy to the preparation of 32 from 26 via 28 and 30, with ester
32 being an intermediate in the enantioselective synthesis of (–)-blennolide A(ent-5a), diastereomer 31 was
synthesized from 25 via 27 and 29 by a Wittig-Horner reaction followed by the introduction of a methyl
group at C-3 (numbering as in 27).
Scheme 5. Syntheses of 31 and 32: a) AD-mix-α, CH3SO2NH2, tBuOH/H2O (1:1), rt, 4 d, 95%, (syn/anti =
1:2.4); b) 2,6-lutidine, TBSOTf, CH2Cl2, 0 °C, 2.5 h, quant.; c) HF∙pyridine, THF/pyridine, 0 °C, 1 h then rt,
26 h, 90% (9% diol); d) DMP, CH2Cl2, rt, 2 h, 94%; e) (MeO)2P(O)CH2CO2Me, NaH, THF, 0 °C →rt, 2 h,
100%, (E/Z = 15.6:1); f) CuBr · Me2S, MeLi, TMSCl, THF, –35 °C, 1 h, 94%; g) H2 (1 atm), 10 mol% Pd/C,
EtOAc, rt, 1 h, 100%; h) DMP, CH2Cl2, rt, 2 h, 92%; i) KOH, I2, MeOH, rt, 4.5 h, 98%; j)
(MeO)2P(O)CH2CO2Me, NaH, THF, 0 °C → rt, 1.5 h, 100%, (E/Z = 4.5:1); k) CuBr · Me2S, MeLi, TMSCl,
THF, –35 °C, 1 h, 91%; l) H2 (1 atm), 15 mol% Pd/C, MeOH, HOAc, rt, 26 h, 100%; m) DMP, CH2Cl2, rt,
2 h, 95%; n) KOH, I2, MeOH, rt, 4 h, 100%; RL = chromanyl.

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Thus, the Wittig-Horner reaction of 25 with (MeO)2P(O)CH2CO2Me and sodium hydride in THF led to
the corresponding -unsaturated ester quantitatively with a very good selectivity (E/Z = 15.6:1). The
E-diastereomer E-27 was then subjected to a Michael addition using CuBr · Me2S, methyl lithium and
TMSCl to yield 29a in 94% yield as the exclusive diastereomer. This stereochemical outcome can be
rationalized as a result of a Felkin-Anh transition state without any chelating effects.9 The assigned
relative configuration of 30 was confirmed by comparison of the NMR data of (–)-blennolide A (ent-5a)
with the natural product (+)-blennolide A. In analogy we rationalized the relative configuration of 29a
using the same Felkin-Anh transition state model as for 30. Subsequent hydrogenolysis of the benzyl
group with palladium on charcoal and oxidation of the resulting primary alcohol using DMP and KOH/I2
in methanol10 led to the methyl ester 31 in 90% over 3 steps via 29b and 29c. Having successfully
prepared the diastereomeric chromanes 31 and 32 the stage was set for the lactonization and benzylic
oxidation.
Scheme 6. Syntheses of γ-lactonyl chromanones ent-3c and ent -3d: a) TBAF·3 H2O, THF, rt, 1 h, 86%; b)
KMnO4, 15% aq. MgSO4-solution, acetone, ultrasound, 60 °C, 10 h, 68%, 73% brsm; c) BBr3, CH2Cl2,
–78 °C, 30 min, for ent-3c: 84%, for ent-3d: 83%; d) TBAF·3 H2O, THF, rt, 100 min, 88%; e) Rh2(cap)4
(3 × 1.0 mol%), tBuOOH, NaHCO3, DCE, 40 °C, 25.5 h, 63%.
Both esters immediately cyclized upon exposure to tetrabutylammonium fluoride (TBAF · 3 H2O) to give
the desired lactones 33 and 35 in 86% and 88% yield, respectively (Scheme 6). To adress the benzylic
oxidation of 33 and 35, we used potassium permanganate,11 dirhodium-tetrakiscaprolactamate

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(36)/tert-butylhydroperoxide (tBuOOH)12 and Mn(OAc)3/tBuOOH13 as oxidizing agents. Treatment of
lactone 33 with potassium permanganate in an ultrasonic bath afforded chromanone 34 in 68% yield. For
the synthesis of 37 from 35 the use of catalytic amounts of dirhodium-tetrakiscaprolactamate (36), NaHCO3
and an excess of tBuOOH gave the highest yield with 63%. Finally, cleavage of the methyl ether moiety in
34 and 37 with BBr3 in dichloromethane at –78 °C led to ent-3c and ent-3d in 84% and 83% yield,
respectively. However, as was the case in the work of Porco et al.,3c the NMR data of compounds ent-3c and
ent-3d were not in agreement with those reported for the natural product implying that the published
structure of 3 is not correct or the natural product contained some impurities. Unfortunately, we were not
able to compare our spectroscopic data with the original spectra, since Guo et al. did not reply to our
request.
Significant differences in the 1H- and 13C-NMR spectra were found for 3-Hb, 2’-H, 4’-Ha and 4’-Hb with δ =
3.46 ppm (d, J = 17.1 Hz), 4.34 ppm (d, J = 3.6 Hz), 2.20 ppm (dd, J = 17.7, 3.9 Hz) and 2.99 ppm (dd, J =
17.7, 9.6 Hz) for 3c and δ = 3.17 ppm (d, J = 17.1 Hz), 4.42 ppm (d, J = 3.9 Hz), 2.20 ppm (dd, J = 17.1,
3.9 Hz) and 2.87 ppm (dd, J = 17.1, 9.3 Hz) for 3d. The corresponding signals of the natural product are δ =
3.53 ppm (d, J = 17.4 Hz), 4.97 ppm (d, J = 6.6 Hz), 2.41 ppm (dd, J = 17, 7 Hz) and 2.73 ppm (dd, J = 17,
7 Hz).
For the synthesis of the dimeric paecilin A (1) (Scheme 7) we have chosen a one pot
borylation/Suzuki-Miyaura reaction.14 In order to access the desired coupling partners, we halogenated
diverse chromanes and chromanones and subjected them to Suzuki conditions. A bromination of 34 and 37
(= 22 without stereochemistry) to give 21 was not suitable, however bromination of 31 at C-8 with
tetrabutylammonium tribromide (TBABr3) provided 38 in 91% yield with high selectivity.15 After
considerable optimization, we were pleased to observe that reaction of 38 with 10 mol% Pd(OAc)2,
25 mol% S-Phos, (Bpin)2 and Cs2CO3 at 50 °C for 21 h led to the desired dimer 39 in 32% yield. In addition,
62% of the debrominated compound 31 and some starting material 38 were isolated. Desilylation of 39
using triethylamine trihydrofluoride (NEt3 · 3 HF) and cleavage of the methyl ether moieties with BBr3
gave 41 in 66% yield over 2 steps. The brominated diastereomer 42, which was obtained from 32 in 83%
yield using TBABr3, did not dimerize to 43 under various reaction conditions. This illustrates that the
dimerization is a very sensitive transformation and even slight stereochemical variations impede the
reaction. Comparison of the spectroscopic data of 41 again failed to match those published for paecelin A
(1).

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Scheme 7. Synthesis of 41: a) TBABr3, THF/H2O (1:1), rt, 23 h, 91%; b) 10 mol% Pd(OAc)2, 25 mol%
S-Phos, (Bpin)2, Cs2CO3, H2O, THF, 50 °C, 21 h, 32% (+ 62% starting material 31); c) NEt3 · 3 HF,
1,4-dioxane, 60 °C, 7 d, 98%; d) BBr3, CH2Cl2, –78 °C, 30 min, 67%; e) TBABr3, THF/H2O (1:1), rt, 22 h,
83%.
CONCLUSION
For the structural determination of paecilin A (1) and B (3) we prepared the almost enantiopure homo dimer
41 and two diastereomeric monomers ent-3c and ent-3d. Their spectroscopic data however did not match
the published information. The closest fit exists for 3b, prepared by Porco et al.,3c in which only the signal
for 3-Hb differs significantly with δ = 3.25 ppm (d, J = 17.3 Hz) instead of δ = 3.53 ppm (d, J = 17.3 Hz).
EXPERIMENTAL
Synthesis of the vinylchroman 20
(S)-2-(Benzyloxymethyl)-5-methoxy-2-vinylchroman (20): A solution of Pd(OTFA)2 (121 mg,
365 µmol, 10 mol%) and (S,S)-iPr-BOXAX (9b) (174 mg, 365 µmol, 10 mol%) in MeOH (3.6 mL) was
stirred at rt for 30 min. After addition of a solution of phenol E/Z-19 (E/Z = 1:1.7, 1.14 g, 3.65 mmol,
1.00 eq.) in MeOH (5.4 mL) and p-benzoquinone (1.58 g, 14.6 mmol, 4.00 eq.) the mixture was heated at
60 °C for 24 h and then cooled to rt. Filtration over a pad of silica gel (15  6 cm, washing with
petroleum ether/EtOAc = 10:1, TLC monitoring), evaporation of the solvent in vacuo and column
chromatography on silica gel (petroleum ether/EtOAc = 30:1) provided vinylchroman 20 as a colorless oil

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(900 mg, 2.90 mmol, 79%, 96% ee). Analytical HPLC (column: Daicel Chiralcel OD): wavelength:
205 nm, flow: 0.8 mL/min, eluent: n-hexane/i-PrOH = 99:1; tR = 12.0 min, (–)-(S)-20, 98.0%;
23
tR = 17.0 min, (+)-(R)-20, 2.0%; 96% ee,  = 1.83. Optical Rotation: []D –75.2 (c 0.19, CHCl3).
1
TLC: Rf = 0.35 (petroleum ether/EtOAc = 20:1). H-NMR (300 MHz, CDCl3): δ = 1.87–2.08 (m, 2 H,
3-H2), 2.44 (ddd, J = 17.1, 10.8, 6.6 Hz, 1 H, 4-Ha), 2.73 (ddd, J = 17.1, 4.8, 3.9 Hz, 1 H, 4-Hb), 3.53 (d,
J = 16.5 Hz, 1 H, CHaOBn), 3.57 (d, J = 16.5 Hz, 1 H, CHbOBn), 3.79 (s, 3 H, 5-OCH3), 4.59 (d,
J = 12.3 Hz, 1 H, OCHaPh), 4.63 (d, J = 12.3 Hz, 1 H, OCHbPh), 5.17 (dd, J = 10.8, 1.5 Hz, 1 H, 2'-Ha),
5.25 (dd, J = 17.4, 1.5 Hz, 1 H, 2'-Hb), 5.85 (dd, J = 17.4, 10.8 Hz, 1 H, 1'-H), 6.40 (d, J = 8.1 Hz, 1 H,
6-H), 6.58 (d, J = 8.1 Hz, 1 H, 8-H), 7.06 (t, J = 8.1 Hz, 1 H, 7-H), 7.23–7.38 (m, 5 H, 5 × Ph-H) ppm.
13C-NMR (125 MHz, CDCl3): δ = 16.4 (C-4), 26.6 (C-3), 55.5 (5-OCH3), 73.7 (OCH2Ph), 75.6
(CH2OBn), 78.8 (C-2), 101.6 (C-6), 109.8 (C-8), 110.8 (C-4a), 116.2 (C-2'), 126.9 (C-7), 127.5 (Ph-Cp),
127.6 (Ph-Co), 128.3 (Ph-Cm), 137.8 (C-1'), 138.3 (Ph-Ci), 154.4 (C-8a), 157.5 (C-5) ppm. IR (film):
ν(cm-1) = 2934, 2856, 1592, 1468, 1409, 1345, 1315, 1267, 1250, 1193, 1167, 1096, 1028, 929, 773, 738,
698. UV (CH3OH): λmax (lg ) = 204.0 nm (4.701), 271.5 (3.113), 279.0 (3.121). MS (ESI): m/z
(%) = 643.3 (53) [2M+Na]+, 333.2 (100) [M+Na]+, 311.2 (25) [M+H]+. Calcd for C20H22O3: 311.1642
[M+H]+, Found: 311.1641 [M+H]+ (ESI-HRMS).
Syntheses of the lactonyl chromanones ent-3c and ent-3d
Methyl (S)-5-Methoxy-2-[(2S,3S)-3-methyl-5-oxotetrahydrofuran-2-yl]chroman-2carboxylate (33):
A solution of chroman 31 (318 mg, 681 µmol, 1.00 eq.) in THF (9.5 mL) was treated with TBAF·3 H2O
(430 mg, 1.36 mmol, 2.00 eq.) at rt and the reaction mixture was stirred at rt for 1 h. After addition of
silica gel (1.5 g) the solvent was evaporated in vacuo. Column chromatography on silica gel (petroleum
ether/EtOAc = 4:1) furnished chroman 33 as a colorless foam (187 mg, 584 µmol, 86%). TLC: Rf = 0.22
1
(petroleum ether/EtOAc = 4:1). H-NMR (300 MHz, CDCl3): δ = 1.07 (d, J = 7.2 Hz, 3 H, 3'-CH3), 2.11
(dd, J = 17.7, 3.6 Hz, 1 H, 4'-Ha), 2.19–2.34 (m, 3 H, 3-H2, 4-Ha), 2.66–2.79 (mc, 1 H, 3'-H), 2.81–2.93
(m, 1 H, 4-Hb), 3.02 (dd, J = 17.7, 9.3 Hz, 1 H, 4'-Hb), 3.72 (s, 3 H, COOCH3), 3.77 (s, 3 H, 5-OCH3),
4.44 (d, J = 3.0 Hz, 1 H, 2'-H), 6.41 (dd, J = 8.4, 0.9 Hz, 1 H, 6-H), 6.49 (dd, J = 8.4, 0.9 Hz, 1 H, 8-H),
7.05 (t, J = 8.4 Hz, 1 H, 7-H) ppm. 13C-NMR (125 MHz, CDCl3): δ = 16.5 (C-4), 20.8 (3'-CH3), 25.5
(C-3), 30.3 (C-3'), 36.4 (C-4'), 52.8 (COOCH3), 55.4 (5-OCH3), 82.1 (C-2), 87.7 (C-2'), 102.6 (C-6),
109.4 (C-8), 109.8 (C-4a), 127.3 (C-7), 153.8 (C-8a), 157.4 (C-5), 171.0 (COOCH3), 176.5 (C-5') ppm.
-1
~
IR (neat): v (cm ) = 2949, 1777, 1757, 1731, 1605, 1591, 1467, 1449, 1440, 1344, 1284, 1272, 1247,
1171, 1131, 1086, 1018, 965, 773. UV (CH3OH): λmax (lg ) = 272.0 nm (3.132), 279.0 (3.127). MS
(ESI): m/z (%) = 663.3 (100) [2M+Na]+, 343.1 (26) [M+Na]+. Calcd for C17H20O6: 343.1158 [M+Na]+,

HETEROCYCLES, Vol. 88, No. 2, 2014
1111
Found: 343.1152 [M+Na]+ (ESI-HRMS).
Methyl (S)-5-Methoxy-2-[(2R,3R)-3-methyl-5-oxotetrahydrofuran-2-yl]chroman-2carboxylate (35):
A solution of chroman 32 (900 mg, 1.93 mmol, 1.00 eq.) in THF (27 mL) was treated with TBAF·3 H2O
(1.22 g, 3.86 mmol, 2.00 eq.) at rt and the reaction mixture was stirred at rt for 100 min. After addition of
silica gel (3.9 g) the solvent was evaporated in vacuo. Column chromatography on silica gel (petroleum
ether/EtOAc = 4:1  3:1) furnished chroman 35 as a colorless foam (542 mg, 1.69 mmol, 88%). TLC: Rf
= 0.19 (petroleum ether/EtOAc = 4:1). 1H-NMR (300 MHz, CDCl3): δ = 1.23 (d, J = 7.2 Hz, 3 H, 3'-CH3),
1.76–1.90 (m, 1 H, 3-Ha), 2.12 (dd, J = 17.7, 3.9 Hz, 1 H, 4'-Ha), 2.22–2.41 (m, 2 H, 3-Hb, 4-Ha),
2.61–2.76 (mc, 1 H, 3'-H), 2.81–2.92 (m, 1 H, 4-Hb), 2.90 (dd, J = 17.7, 9.3 Hz, 1 H, 4'-Hb), 3.70 (s, 3 H,
COOCH3), 3.77 (s, 3 H, 5-OCH3), 4.45 (d, J = 3.3 Hz, 1 H, 2'-H), 6.42 (dd, J = 8.1, 0.6 Hz, 1 H, 6-H),
13
6.54 (dd, J = 8.1, 0.6 Hz, 1 H, 8-H), 7.07 (t, J = 8.1 Hz, 1 H, 7-H) ppm. C-NMR (125 MHz, CDCl3): δ
= 16.2 (C-4), 21.2 (3'-CH3), 25.0 (C-3), 29.7 (C-3'), 36.4 (C-4'), 52.9 (COOCH3), 55.4 (5-OCH3), 81.8
(C-2), 89.0 (C-2'), 102.6 (C-6), 109.4 (C-8), 109.5 (C-4a), 127.5 (C-7), 153.6 (C-8a), 157.4 (C-5), 170.8
-1
~
(COOCH3), 176.1 (C-5') ppm. IR (neat): v (cm ) = 2956, 1772, 1751, 1733, 1606, 1591, 1470, 1347,
1268, 1248, 1170, 1145, 1082, 972, 769, 710, 514. UV (CH3CN): λmax (lg ) = 203.0 nm (4.630), 273.0
(3.150), 279.0 (3.148), 300.0 (2.433). MS (ESI): m/z (%) = 663.3 (100) [2M+Na]+, 343.1 (34) [M+Na]+.
Calcd for C17H20O6: 343.1158 [M+Na]+, Found: 343.1155 [M+Na]+ (ESI-HRMS).
Methyl (S)-5-Methoxy-2-[(2S,3S)-3-methyl-5-oxotetrahydrofuran-2-yl]-4-oxochroman-2carboxylate
(34): Method A (Mn-catalysed oxidation): A solution of chroman 33 (40.0 mg, 125 µmol, 1.00 eq.) and
tert-butyl hydroperoxide (230 µL of a 5.5 M solution in decane, 1.25 mmol, 10.0 eq.) in EtOAc (0.45 mL)
was treated with powdered molecular sieves 3 Å (45 mg) and the resulting mixture was stirred at rt for
30 min. After addition of Mn(OAc)3·2 H2O (6.70 mg, 25.0 µmol, 20 mol%) stirring was continued for 2 d
before additional Mn(OAc)3·2 H2O (3.40 mg, 12.7 µmol, 10 mol%), tert-butyl hydroperoxide (115 µL of
a 5.5 M solution in decane, 633 µmol, 5.06 eq.) and EtOAc (0.2 mL) were added. The mixture was stirred
for further 24 h at rt and filtered over silica gel (eluting with EtOAc). After concentration in vacuo and
column chromatography on silica gel (petroleum ether/EtOAc = 3:2) chromanone 34 was obtained as a
colorless solid (29.3 mg, 87.6 µmol, 70%). Method B (Rh-catalysed oxidation): A solution of chroman 33
(40.0 mg, 125 µmol, 1.00 eq.) and dirhodium-tetrakiscaprolactamate (36) (410 µg, 625 nmol, 0.5 mol%)
in dichloroethane (0.5 mL) was treated with NaHCO3 (5.30 mg, 62.5 µmol, 0.50 eq.). tert-Butyl
hydroperoxide (114 µL of a 5.5 M solution in decane, 625 µmol, 5.00 eq.) was added and the resulting
deep-red solution was heated with stirring at 40 °C. After 3 h the mixture was treated with additional
dirhodium-tetrakiscaprolactamate (36) (410 µg, 625 nmol, 0.5 mol%) and tert-butyl hydroperoxide

1112
HETEROCYCLES, Vol. 88, No. 2, 2014
(114 µL of a 5.5 M solution in decane, 625 µmol, 5.00 eq.). Stirring was continued at 40 °C for 19 h
before additional dirhodium-tetrakiscaprolactamate (36) (820 µg, 1.25 µmol, 1 mol%) and tert-butyl
hydroperoxide (228 µL of a 5.5 M solution in decane, 1.25 mmol, 10.0 eq.) were added. After stirring at
40 °C for further 8 h the solids were removed by filtration over silica gel (eluting with EtOAc). After
evaporation of the solvent in vacuo and column chromatography on silica gel (petroleum
ether/EtOAc = 3:2) chromanone 34 was obtained as a colorless solid (28.0 mg, 83.7 µmol, 67%). Method
C (KMnO4 oxidation): A suspension of chroman 33 (50.0 mg, 156 µmol, 1.00 eq.), potassium
permanganate (99.0 mg, 624 µmol, 4.00 eq.), 15% aq. MgSO4 solution (0.25 mL) and acetone (1 mL) in a
sealed tube was kept for 4 h at 60 °C in ultrasonic bath. A second portion of potassium permanganate
(99.0 mg, 624 µmol, 4.00 eq.), 15% aq. MgSO4 solution (0.25 mL) and acetone (0.5 mL) was added
before the irradiation was continued for 3 h at 60 °C. After addition of a third portion of potassium
permanganate (150 mg, 949 µmol, 8.00 eq.) and 15% aq. MgSO4 solution (0.38 mL) the reaction mixture
was irradiated for further 3 h bei 60 °C, cooled to rt and passed through silica gel in column (6  3 cm,
washing with EtOAc, TLC monitoring). After evaporation of the solvent in vacuo column
chromatography on silica gel (petroleum ether/EtOAc = 3:2) furnished chromanone 34 as a colorless solid
(35.5 mg, 106 µmol, 68%, 73% brsm). Optical Rotation: [] 2D4 –36.3 (c 0.60, CHCl3). TLC: Rf = 0.24
(petroleum ether/EtOAc = 1:1). 1H-NMR (300 MHz, CDCl3): δ = 1.14 (d, J = 7.2 Hz, 3 H, 3'-CH3), 2.18
(dd, J = 17.7, 4.2 Hz, 1 H, 4'-Ha), 2.71–2.85 (mc, 1 H, 3'-H), 2.93 (d, J = 16.2 Hz, 1 H, 3-Ha), 2.98 (dd,
J = 17.7, 9.3 Hz, 1 H, 4'-Hb), 3.35 (d, J = 16.2 Hz, 1 H, 3-Hb), 3.68 (s, 3 H, COOCH3), 3.85 (s, 3 H,
5-OCH3), 4.34 (d, J = 3.3 Hz, 1 H, 2'-H), 6.51 (dd, J = 8.4, 0.9 Hz, 1 H, 6-H), 6.58 (dd, J = 8.4, 0.9 Hz,
13
1 H, 8-H), 7.38 (t, J = 8.4 Hz, 1 H, 7-H) ppm. C-NMR (125 MHz, CDCl3): δ = 20.5 (3'-CH3), 29.6
(C-3'), 36.3 (C-4'), 42.4 (C-3), 53.3 (COOCH3), 56.2 (5-OCH3), 84.1 (C-2), 86.5 (C-2'), 104.7 (C-6),
109.8 (C-8), 110.6 (C-4a), 136.4 (C-7), 160.3 (C-5), 161.0 (C-8a), 169.1 (COOCH3), 175.7 (C-5'), 187.4
-1
~
(C-4) ppm. IR (neat): v (cm ) = 2973, 1779, 1747, 1694, 1601, 1578, 1471, 1441, 1291, 1259, 1199,
1164, 1012, 788, 742, 580, 529. UV (CH3CN): λmax (lg ) = 214.0 nm (4.187), 265.0 (3.907), 327.0
(3.564). MS (ESI): m/z (%) = 691.2 (100) [2M+Na]+, 357.1 (28) [M+Na]+. Calcd for C17H18O7: 357.0950
[M+Na]+, Found: 357.0946 [M+Na]+ (ESI-HRMS).
Methyl (S)-5-Methoxy-2-[(2R,3R)-3-methyl-5-oxotetrahydrofuran-2-yl]-4-oxochroman-2-carboxylate
(37): A solution of chroman 35 (90.0 mg, 281 µmol, 1.00 eq.) and dirhodium-tetrakiscaprolactamate
(1.84 mg, 2.81 µmol, 1 mol%) in dichloroethane (1.1 mL) was treated with NaHCO3 (11.8 mg, 141 µmol,
0.50 eq.). tert-Butyl hydroperoxide (510 µL of a 5.5 M solution in decane, 2.81 mmol, 10.0 eq.) was
added and the resulting deep-red solution was heated with stirring at 40 °C. After 4 h the mixture was

HETEROCYCLES, Vol. 88, No. 2, 2014
1113
treated with additional dirhodium-tetrakiscaprolactamate (1.84 mg, 2.81 µmol, 1 mol%) and tert-butyl
hydroperoxide (510 µL of a 5.5 M solution in decane, 2.81 mmol, 10.0 eq.). Stirring was continued at
40 °C for 15 h before additional dirhodium-tetrakiscaprolactamate (1.84 mg, 2.81 µmol, 1 mol%) and
tert-butyl hydroperoxide (510 µL of a 5.5 M solution in decane, 2.81 mmol, 10.0 eq.) were added. After
stirring at 40 °C for further 6.5 h the solids were removed by filtration over silica gel (eluting with
EtOAc). After evaporation of the solvent in vacuo and column chromatography on silica gel (petroleum
ether/EtOAc = 1:1) chromanone 37 was obtained as a colorless solid (59.0 mg, 176 µmol, 63%).
Mn-catalysed oxidation (51% yield, 64% brsm) and KMnO4 oxidation (47% yield) were performed
according to the described procedure for synthesis of 34. TLC: Rf = 0.21 (petroleum ether/EtOAc = 1:1).
1H-NMR (300 MHz, CDCl3): δ = 1.25 (d, J = 6.9 Hz, 3 H, 3'-CH3), 2.19 (dd, J = 17.1, 3.6 Hz, 1 H, 4'-Ha),
2.74–2.89 (mc, 1 H, 3'-H), 2.88 (dd, J = 17.1, 9.3 Hz, 1 H, 4'-Hb), 2.93 (d, J = 16.2 Hz, 1 H, 3-Ha), 3.06 (d,
J = 16.2 Hz, 1 H, 3-Hb), 3.68 (s, 3 H, COOCH3), 3.88 (s, 3 H, 5-OCH3), 4.41 (d, J = 3.6 Hz, 1 H, 2'-H),
6.54 (dd, J = 8.4, 0.9 Hz, 1 H, 6-H), 6.65 (dd, J = 8.4, 0.9 Hz, 1 H, 8-H), 7.41 (t, J = 8.4 Hz, 1 H, 7-H)
ppm. 13C-NMR (125 MHz, CDCl3): δ = 21.0 (3'-CH3), 29.8 (C-3'), 36.1 (C-4'), 41.6 (C-3), 53.4
(COOCH3), 56.2 (5-OCH3), 84.1 (C-2), 87.7 (C-2'), 104.9 (C-6), 110.1 (C-8), 110.9 (C-4a), 136.8 (C-7),
-1
~
160.5 (C-5), 161.2 (C-8a), 168.9 (COOCH3), 175.4 (C-5'), 186.4 (C-4) ppm. IR (neat): v (cm ) = 1767,
1755, 1674, 1601, 1574, 1471, 1440, 1336, 1257, 1178, 1100, 1076, 1001, 790, 742, 650, 576, 520. UV
(CH3CN): λmax (lg ) = 265.0 nm (3.995), 328.0 (3.677). MS (ESI): m/z (%) = 691.2 (100) [2M+Na]+,
357.1 (40) [M+Na]+. Calcd for C17H18O7: 357.0950 [M+Na]+, Found: 357.0945 [M+Na]+ (ESI-HRMS).
Methyl (S)-5-Hydroxy-2-[(2S,3S)-3-methyl-5-oxotetrahydrofuran-2-yl]-4-oxochroman-2carboxylate
(ent-3c): A solution of BBr3 (7.78 mL of a 1.0 M solution in CH2Cl2, 7.78 mmol, 10.0 eq.) was added
slowly to a stirred solution of chromanone 34 (260 mg, 778 µmol, 1.00 eq.) in CH2Cl2 (40 mL) at –78 °C.
Stirring was continued for 30 min at –78 °C before being quenched with sat. aq. NaHCO3 solution (7 mL)
at –78 °C. The organic layer was separated and the aqueous layer was extracted with EtOAc (3 × 40 mL).
The combined organic layers were dried over Na2SO4 and the solvent was evaporated in vacuo. After
column chromatography on silica gel (petroleum ether/EtOAc = 2:1) chromanone ent-3c was obtained as
a colorless solid (209 mg, 653 µmol, 84%). Optical Rotation: [] 2D4 –68.1 (c 1.20, CHCl3). TLC: Rf =
1
0.31 (petroleum ether/EtOAc = 2:1). H-NMR (300 MHz, CDCl3): δ = 1.16 (d, J = 7.2 Hz, 3 H, 3'-CH3),
2.20 (dd, J = 17.7, 3.9 Hz, 1 H, 4'-Ha), 2.76–2.90 (mc, 1 H, 3'-H), 2.99 (dd, J = 17.7, 9.6 Hz, 1 H, 4'-Hb),
3.05 (d, J = 17.1 Hz, 1 H, 3-Ha), 3.46 (d, J = 17.1 Hz, 1 H, 3-Hb), 3.72 (s, 3 H, COOCH3), 4.34 (d,
J = 3.6 Hz, 1 H, 2'-H), 6.47 (dd, J = 8.4, 0.9 Hz, 1 H, 8-H), 6.52 (dd, J = 8.4, 0.9 Hz, 1 H, 6-H), 7.37 (t,
J = 8.4 Hz, 1 H, 7-H), 11.42 (sbr, 1 H, 5-OH) ppm. 13C-NMR (125 MHz, CDCl3): δ = 20.5 (3'-CH3), 29.6

1114
HETEROCYCLES, Vol. 88, No. 2, 2014
(C-3'), 36.3 (C-4'), 40.5 (C-3), 53.5 (COOCH3), 84.2 (C-2), 86.4 (C-2'), 107.4 (C-8, C-4a), 110.4 (C-6),
~
138.8 (C-7), 159.2 (C-8a), 161.8 (C-5), 169.0 (COOCH3), 175.5 (C-5'), 194.8 (C-4) ppm. IR (neat): v
(cm-1) = 2976, 2955, 1779, 1738, 1639, 1623, 1577, 1466, 1342, 1293, 1201, 1179, 1156, 1048, 1008, 840,
802, 728, 637, 579, 515. UV (CH3CN): λmax (lg ) = 271.0 nm (3.930), 347.0 (3.485). MS (ESI): m/z
(%) = 663.2 (100) [2M+Na]+, 343.1 (31) [M+Na]+. Calcd for C16H16O7: 343.0794 [M+Na]+, Found:
343.0796 [M+Na]+ (ESI-HRMS).
Methyl (S)-5-Hydroxy-2-[(2R,3R)-3-methyl-5-oxotetrahydrofuran-2-yl]-4-oxochroman2-carboxylate
(ent-3d): A solution of BBr3 (18.5 mL of a 1.0 M solution in CH2Cl2, 18.5 mmol, 10.0 eq.) was added
slowly to a stirred solution of chromanone 37 (620 mg, 1.85 mmol, 1.00 eq.) in CH2Cl2 (90 mL) at
–78 °C. Stirring was continued for 30 min at –78 °C before being quenched with sat. aq. NaHCO3
solution (170 mL) at –78 °C. The organic layer was separated and the aqueous layer was extracted with
EtOAc (3 × 80 mL). The combined organic layers were dried over Na2SO4 and the solvent was
evaporated in vacuo. After column chromatography on silica gel (petroleum ether/EtOAc = 2:1)
chromanone ent-3d was obtained as a pale-yellow foam (492 mg, 1.54 mmol, 83%). Optical Rotation:
23
D
[]
–39.1 (c 1.02, CHCl3). TLC: Rf = 0.61 (petroleum ether/EtOAc = 1:1). 1H-NMR
(300 MHz, CDCl3): δ = 1.26 (d, J = 6.9 Hz, 3 H, 3'-CH3), 2.20 (dd, J = 17.1, 3.9 Hz, 1 H, 4'-Ha),
2.74–2.89 (mc, 1 H, 3'-H), 2.87 (dd, J = 17.1, 9.3 Hz, 1 H, 4'-Hb), 3.01 (d, J = 17.1 Hz, 1 H, 3-Ha), 3.17 (d,
J = 17.1 Hz, 1 H, 3-Hb), 3.70 (s, 3 H, COOCH3), 4.42 (d, J = 3.9 Hz, 1 H, 2'-H), 6.51 (d, J = 8.4 Hz, 1 H,
8-H), 6.54 (d, J = 8.4 Hz, 1 H, 6-H), 7.39 (t, J = 8.4 Hz, 1 H, 7-H), 11.41 (sbr, 1 H, 5-OH) ppm. 13C-NMR
(125 MHz, CDCl3): δ = 20.8 (3'-CH3), 29.9 (C-3'), 36.0 (C-4'), 39.7 (C-3), 53.6 (COOCH3), 84.2 (C-2),
87.5 (C-2'), 107.6 (C-4a), 107.6 (C-8), 110.6 (C-6), 139.0 (C-7), 159.1 (C-8a), 161.9 (C-5), 168.8
-1
~
(COOCH3), 175.1 (C-5'), 193.9 (C-4) ppm. IR (neat): v (cm ) = 2957, 1784, 1738, 1646, 1626, 1579,
1461, 1354, 1228, 1202, 1171, 1051, 1008, 796, 731, 638. UV (CH3OH): λmax (lg ) = 206.0 nm (4.246),
272.0 (3.945), 349.0 (3.471). MS (ESI): m/z (%) = 663.2 (100) [2M+Na]+, 343.1 (20) [M+Na]+. Calcd for
C16H16O7: 343.0794 [M+Na]+, Found: 343.0790 [M+Na]+ (ESI-HRMS).
Synthesis of the dimeric compound 41
Methyl
(S)-8-Bromo-2-[(1S,2S)-1-(tert-butyldimethylsilyloxy)-4-methoxy-2-methyl-4oxo-butyl]-5-
methoxy-4-oxochroman-2-carboxylate (38): nBu4NBr3 (145 mg, 301 µmol, 1.02 eq.) was added to a
solution of chromanone 31 (142 mg, 295 µmol, 1.00 eq.) in THF/H2O (1:1, 1.4 mL) at rt and the reaction
mixture was stirred for 23 h at rt. After concentration in vacuo and column chromatography on silica gel
(petroleum ether/EtOAc = 3:1) chromanone 38 was obtained as a colorless oil (150 mg, 268 µmol, 91%).

HETEROCYCLES, Vol. 88, No. 2, 2014
1115
Optical Rotation: [] 2D5 +12.5 (c 1.70, CHCl3). TLC: Rf = 0.31 (petroleum ether/EtOAc = 2:1).
1H-NMR (300 MHz, CDCl3): δ = 0.10 (s, 3 H, Si(CH3)a), 0.15 (s, 3 H, Si(CH3)b), 0.89 (s, 9 H,
SiC(CH3)3), 1.11 (d, J = 6.9 Hz, 3 H, 2'-CH3), 2.19 (dd, J = 16.5, 10.5 Hz, 1 H, 3'-Ha), 2.38–2.53 (mc, 1 H,
2'-H), 2.88 (d, J = 16.2 Hz, 1 H, 3-Ha), 3.23 (dd, J = 16.5, 3.0 Hz, 1 H, 3'-Hb), 3.25 (d, J = 16.2 Hz, 1 H,
3-Hb), 3.64 (s, 3 H, 2-COOCH3), 3.65 (s, 3 H, 4'-OCH3), 3.86 (s, 3 H, 5-OCH3), 4.00 (d, J = 2.1 Hz, 1 H,
1'-H), 6.43 (d, J = 9.0 Hz, 1 H, 6-H), 7.60 (d, J = 9.0 Hz, 1 H, 7-H) ppm. 13C-NMR (125 MHz, CDCl3): δ
= –4.2, –3.2 (Si(CH3)2), 18.5 (SiC(CH3)3), 19.9 (2'-CH3), 26.1 (SiC(CH3)3), 32.7 (C-2'), 36.6 (C-3'), 43.1
(C-3), 51.5 (4'-OCH3), 53.1 (2-COOCH3), 56.3 (5-OCH3), 78.1 (C-1'), 88.4 (C-2), 102.2 (C-8), 105.4
(C-6), 111.8 (C-4a), 139.1 (C-7), 157.8 (C-8a), 159.4 (C-5), 170.2 (2-COOCH3), 173.6 (C-4'), 188.2 (C-4)
-1
~
ppm. IR (neat): v (cm ) = 2953, 2931, 1735, 1639, 1587, 1471, 1436, 1315, 1251, 1099, 1054, 832,
776, 734, 528. UV (CH3CN): λmax (lg ) = 194.0 nm (4.426), 268.0 (3.813), 336.0 (3.592). MS (ESI): m/z
(%) = 1141.3 (100) [2M+Na]+, 1063.4 (9) [2M–Br+Na]+, 583.1 (29) [M+Na]+, 561.2 (48) [M+H]+, 481.3
(6) [M–Br+H]+. Calcd for C24H35BrO8Si: 581.1182 [M+Na]+, Found: 581.1177 [M+Na]+ (ESI-HRMS).
Dimethyl (2S,2'S)-2,2'-bis[(1S,2S)-1-(tert-Butyldimethylsilyloxy)-4-methoxy-2-methyl-4-oxobutyl]-
5,5'-dimethoxy-4,4'-dioxo-[8,8'-bichroman]-2,2'-dicarboxylate (39): A solution of chromanone 38
(127 mg, 227 µmol, 1.00 eq.) in THF (8.5 mL) was added to a mixture of Pd(OAc)2 (5.10 mg, 22.7 µmol,
10 mol%), S-Phos (23.3 mg, 56.8 µmol, 25 mol%), Cs2CO3 (148 mg, 454 µmol, 2.00 eq.),
bis(pinacolato)diboron (115 mg, 454 µmol, 2.00 eq.) and water (16.4 µL, 16.4 mg, 908 µmol, 4.00 eq.) at
rt and the reaction mixture was stirred at 50 °C for 21 h. The catalyst was removed by filtration over silica
gel (washing with EtOAc) and the solvent was evaporated in vacuo. Column chromatography on silica
gel (petroleum ether/EtOAc = 2:1  1:1) provided biaryl 39 as a colorless solid (35.0 mg, 36.5 µmol,
32%) and a inseparable mixture of chromanonen 31 and 38 as a pale-yellow oil (77.0 mg, 141 µmol, 62%,
26
D
31:38 = 1:5). Optical Rotation: []
–24.6 (c 0.92, CHCl3). TLC: Rf = 0.11 (petroleum
1
ether/EtOAc = 2:1). H-NMR (300 MHz, CDCl3): δ = 0.06 (s, 6 H, 2 × Si(CH3)a), 0.09 (s, 6 H,
2 × Si(CH3)b), 0.84–0.96 (m, 24 H, 2 × SiC(CH3)3, 2''-CH3, 2'''-CH3), 1.88 (dd, J = 16.8, 10.8 Hz, 2 H,
3''-Ha, 3'''-Ha), 2.05–2.22 (m, 2 H, 2''-H, 2'''-H), 2.38 (d, J = 16.8 Hz, 2 H, 3''-Hb, 3'''-Hb), 2.87 (dd,
J = 15.6 Hz, 2 H, 3-Ha, 3'-Ha), 3.25 (d, J = 15.6 Hz, 2 H, 3-Hb, 3'-Hb), 3.47 (s, 6 H, 4''-OCH3, 4'''-OCH3),
3.63 (sbr, 6 H, 2-COOCH3, 2'-COOCH3), 3.85 (d, J = 1.8 Hz, 2 H, 1''-H, 1'''-H), 3.92 (s, 6 H, 5-OCH3,
5'-OCH3), 6.55 (d, J = 9.0 Hz, 2 H, 6-H, 6'-H), 7.54 (d, J = 9.0 Hz, 2 H, 7-H, 7'-H) ppm. 13C-NMR
(125 MHz, CDCl3): δ = –4.4, –3.4 (Si(CH3)2), 18.4 (SiC(CH3)3), 19.1 (2''-CH3, 2'''-CH3), 26.1 (SiC(CH3)3),
32.9 (C-2'', C-2'''), 35.7 (C-3'', C-3'''), 43.3 (C-3, C-3'), 51.1 (4''-OCH3, 4'''-OCH3), 52.9 (2-COOCH3,
2'-COOCH3), 56.0 (5-OCH3, 5'-OCH3), 78.1 (C-1'', C-1'''), 87.6 (C-2, C-2'), 104.0 (C-6, C-6'), 110.8

1116
HETEROCYCLES, Vol. 88, No. 2, 2014
(C-4a, C-4a'), 118.0 (C-8, C-8'), 139.4 (C-7, C-7'), 158.7 (C-8a, C-8a'), 159.8 (C-5, C-5'), 171.0
-1
~
(2-COOCH3, 2'-COOCH3), 173.2 (C-4'', C-4'''), 189.1 (C-4, C-4') ppm. IR (neat): v (cm ) = 2923,
1728, 1690, 1593, 1572, 1474, 1255, 1166, 1119, 1099, 1039, 827, 772. UV (CH3CN): λmax (lg ) =
193.0 nm (4.679), 247.0 (4.261), 338.0 (3.818). MS (ESI): m/z (%) = 981.4 (100) [M+Na]+. Calcd for
C48H70O16Si2: 981.4100 [M+Na]+, Found: 981.4095 [M+Na]+ (ESI-HRMS).
Dimethyl (2S,2'S)-5,5'-Dimethoxy-2,2'-bis[(2S,3S)-3-methyl-5-oxotetrahydrofuran-2-yl]4,4'-dioxo-
[8,8'-bichroman]-2,2'-dicarboxylate (40): NEt3·3 HF (120 µL, 118 mg, 730 µmol, 25.0 eq.) was added
to a solution of biaryl 39 (28.0 mg, 29.2 µmol, 1.00 eq.) in 1,4-dioxane (1 mL) at rt and the reaction
mixture was stirred at 60 °C for 3 d. After a second addition of NEt3·3 HF (120 µL, 118 mg, 730 µmol,
25.0 eq.) stirring was continued for further 4 d at 60 °C before being quenched by carefully addition of sat.
aq. NaHCO3 solution (8 mL) at 0 °C. The aqueous layer was extracted with EtOAc (3 × 15 mL), the
combined organic layers were dried over Na2SO4 and the solvent was evaporated in vacuo. Column
chromatography on silica gel (petroleum ether/EtOAc = 1:5) furnished compound 40 as a colorless foam
(19.0 mg, 28.5 µmol, 98%). Optical Rotation: [] 2D5 +11.4 (c 0.47, CHCl3). TLC: Rf = 0.12 (petroleum
1
ether/EtOAc = 1:3). H-NMR (300 MHz, CDCl3): δ = 1.00 (d, J = 7.2 Hz, 6 H, 3''-CH3, 3'''-CH3),
1.55–1.86 (m, 4 H, 4''-H2, 4'''-H2), 2.47–2.65 (mc, 2 H, 3''-H, 3'''-H), 2.74 (d, J = 15.9 Hz, 2 H, 3-Ha, 3'-Ha),
3.42 (d, J = 15.9 Hz, 2 H, 3-Hb, 3'-Hb), 3.60 (sbr, 6 H, 2-COOCH3, 2'-COOCH3), 3.90 (s, 6 H, 5-OCH3,
5'-OCH3), 4.28 (sbr, 2 H, 2''-H, 2'''-H), 6.61 (d, J = 8.7 Hz, 2 H, 6-H, 6'-H), 7.13–7.29, 7.43–7.64 (2 × m,
13
2 H, 7-H, 7'-H) ppm. C-NMR (125 MHz, CDCl3): δ = 21.0 (3''-CH3, 3'''-CH3), 29.6 (C-3'', C-3'''), 35.3
(C-4'', C-4'''), 42.3 (C-3, C-3'), 52.5 (2-COOCH3, 2'-COOCH3), 56.4 (5-OCH3, 5'-OCH3), 84.2 (C-2, C-2'),
85.9 (C-2'', C-2'''), 104.0 (C-6, C-6'), 110.6 (C-8, C-8'), 118.1 (C-4a, C-4a'), 138.2 (C-7, C-7'), 158.4
(C-8a, C-8a'), 159.6 (C-5, C-5'), 167.9 (2-COOCH3, 2'-COOCH3), 176.9 (C-5'', C-5'''), 188.0 (C-4, C-4')
-1
~
ppm. IR (neat): v (cm ) = 2958, 1783, 1748, 1684, 1569, 1474, 1254, 1160, 1091, 1011, 749. UV
(CH3CN): λmax (lg ) = 194.0 nm (4.628), 254.0 (4.251), 336.0 (3.899). MS (ESI): m/z (%) = 1355.4 (71)
[2M+Na]+, 689.2 (100) [M+Na]+, 667.2 (60) [2M+H]+. Calcd for C34H34O14: 689.1846 [M+Na]+, Found:
689.1841 [M+Na]+ (ESI-HRMS).
Dimethyl (2S,2'S)-5,5'-Dihydroxy-2,2'-bis[(2S,3S)-3-methyl-5-oxotetrahydrofuran-2-yl]4,4'-dioxo-
[8,8'-bichroman]-2,2'-dicarboxylate (41): A solution of BBr3 (590 µL of a 1.0 M solution in CH2Cl2,
590 µmol, 19.9 eq.) was added slowly to a stirred solution of biaryl 40 (19.0 mg, 29.7 µmol, 1.00 eq.) in
CH2Cl2 (3 mL) at –78 °C. The resulting solution was stirred for 30 min at –78 °C before being quenched
with sat. aq. NaHCO3 solution (10 mL) at –78 °C. The organic layer was separated and the aqueous layer

HETEROCYCLES, Vol. 88, No. 2, 2014
1117
was extracted with EtOAc (3 × 10 mL). The combined organic layers were dried over Na2SO4 and the
solvent was evaporated in vacuo. After column chromatography on silica gel (petroleum
ether/EtOAc = 1:1) biaryl 41 was obtained as a colorless foam (12.7 mg, 19.9 µmol, 67%). Optical
Rotation: [] 2D4 +78.3 (c 0.64, CHCl3). TLC: Rf = 0.28 (petroleum ether/EtOAc = 1:1). H-NMR
1
(300 MHz, CDCl3): δ = 1.05 (d, J = 6.9 Hz, 6 H, 3''-CH3, 3'''-CH3), 1.82 (dd, J = 18.0, 3.6 Hz, 2 H, 4''-Ha,
4'''-Ha), 2.06 (dd, J = 18.0, 9.0 Hz, 2 H, 4''-Hb, 4'''-Hb), 2.39–2.57 (mc, 2 H, 3''-H, 3'''-H), 3.03 (d,
J = 17.4 Hz, 2 H, 3-Ha, 3'-Ha), 3.59 (d, J = 17.4 Hz, 2 H, 3-Hb, 3'-Hb), 3.76 (sbr, 6 H, 2-COOCH3,
2'-COOCH3), 4.26 (d, J = 3.0 Hz, 2 H, 2''-H, 2'''-H), 6.60 (d, J = 8.7 Hz, 2 H, 6-H, 6'-H), 7.47–7.82 (m,
13
2 H, 7-H, 7'-H), 11.61 (sbr, 2 H, 5-OH, 5'-OH) ppm. C-NMR (125 MHz, CDCl3): δ = 20.7 (3''-CH3,
3'''-CH3), 29.7 (C-3'', C-3'''), 35.4 (C-4'', C-4'''), 40.5 (C-3, C-3'), 53.5 (2-COOCH3, 2'-COOCH3), 84.9
(C-2, C-2'), 85.9 (C-2'', C-2'''), 107.5 (C-4a, C-4a'), 109.9 (C-6, C-6'), 115.0 (C-8, C-8'), 140.8 (C-7, C-7'),
156.4 (C-8a, C-8a'), 161.6 (C-5, C-5'), 168.9 (2-COOCH3, 2'-COOCH3), 175.3 (C-5'', C-5'''), 195.3 (C-4,
-1
~
C-4') ppm. IR (neat): v (cm ) = 2960, 1787, 1748, 1646, 1465, 1343, 1152, 1008, 733. UV (CH3CN):
λmax (lg ) = 196.0 (4.534), 256.0 (4.361), 359.0 (3.756). MS (ESI): m/z (%) = 1299.3 (100) [2M+Na]+,
661.2 (59) [M+Na]+. Calcd for C32H30O14: 661.1533 [M+Na]+, Found: 661.1530 [M+Na]+ (ESI-HRMS).
ACKNOWLEDGEMENTS
We thank the Deutsche Forschungsgemeinschaft (DFG), the state of Lower Saxony, the VW-foundation
and the Fonds of the Chemical Industry for generous support. S.J. thanks the CaSuS Program and J.R.R.
thanks the Konrad Adenauer Stiftung for Ph.D. scholarships, J.H. thanks the Dorothea Schlözer Fellowship
Programme and B.G. thanks the Alexander von Humboldt Foundation for postdoctoral scholarships.
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