- A novel and efficient total synthesis of shikonin
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A novel and efficient synthesis of shikonin was accomplished with excellent enantiomeric excess (99.3% ee) and high overall yield (47%) in only six steps. The synthetic strategy involved an efficient Ru(II)-catalyzed asymmetric hydrogenation employing C2-symmetric planar chiral ruthenocene phosphinooxazoline ligand (L-3), followed by the subsequent removal of the methyl protecting groups. Meanwhile, it could be preliminarily confirmed that the chiral side chain of shikonin was difficult to be constructed in one step with both stereoselectivity and α-regioselectivity.
- Wang, Rubing,Guo, Hui,Cui, Jiahua,Li, Shaoshun
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- High performance liquid chromatography resolution method of alkannin raceme and naphthazarin parent nucleus hydroxyl methylated carbonyl oxime derivative of alkannin raceme
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The invention discloses a high performance liquid chromatography resolution method of alkannin raceme and naphthazarin parent nucleus hydroxyl methylated carbonyl oxime derivatives thereof, which comprises the following steps: using high performance liquid chromatography, using amylose-tris [(S)-alpha-methyl benzyl carbamate] as a filler and an n-hexane-isopropanol mixed solvent as a mobile phase, separating high-purity R-(+)-alkannin from an alkannin raceme, separating high-purity S-(+)-alkannin naphthazarin parent nucleus hydroxyl methylated carbonyl oxime derivatives from an alkannin raceme naphthazarin parent nucleus hydroxyl methylated carbonyl oxime derivative, and combining a certain separation and purification means. Therefore, the production efficiency of R-(+)- alkannin is improved, and the efficiency of producing the optically pure alkannin naphthazarin parent nucleus hydroxyl methylated carbonyl oxime derivative by using an intermediate resolution method is improved.
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Paragraph 0036-0045
(2021/04/17)
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- An improved and practical synthesis route to antiproliferative (±)-shikonin and its O-acyl derivatives
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Shikonin and its O-acyl derivatives are attracting increasing levels of attention among medicinal chemists due to their potencies as highly selective cytotoxic agents against cancer cells. However, providing a large number of shikonin-related samples by organic synthesis remains challenging. In the present study, we developed an improved and practical synthesis route to shikonin derivatives by olefin metathesis that has enabled the gram-scale preparation of a prenylated tetramethylnaphthazaline, a key intermediate in the synthesis of shikonin. In addition, a method for the selective cleavage of the acyl protecting groups at the phenolic positions of tri-O-acylated shikonins has been developed that provides concise routes to diverse O-acylshikonin derivatives.
- Ono, Mana,Abe, Shouki,Higai, Koji,Higashi, Shoko,Saito, Setsuo,Saito, Ryota
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p. 738 - 746
(2020/12/09)
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- An efficient multigram synthesis of alkannin and shikonin
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The concise and efficient total syntheses of alkannin (1) and shikonin (2), based on the resolution of a key acid intermediate, are achieved with excellent enantiomeric excesses and high overall yields (99 % ee, 15.6 % for 1 and 99.8 % ee, 11.9 % for 2). The key steps of the synthetic strategy involve the convenient synthesis and separation of a pair of amide diastereoisomers and the mild hydrolysis of the amide to remove the amine chiral auxiliary, together with an efficient deprotection sequence of the methyl protecting groups. The concise and efficient syntheses of alkannin and shikonin remained elusive until recently. We have developed a new method of resolution for achieving the syntheses of alkannin (1) and shikonin (2) in excellentenantiomeric excesses (≥ 99 % ee for 1 and ≥ 99.8 % ee for 2) and high yields (27.5 %) with low cost, which is practical for use in large-scale preparation. Copyright
- Wang, Rubing,Zhou, Shanshan,Jiang, Hudagula,Zheng, Xiaogang,Zhou, Wen,Li, Shaoshun
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p. 1373 - 1379
(2012/04/04)
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- Tigloylshikonin, a new minor shikonin derivative, from the roots and the commercial root extract of Lithospermum erythrorhizon
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Tigloylshikonin, a new shikonin derivative esterified with tiglic acid ((E)-2-methylbut-2-enoic acid), was isolated as a minor pigment from a food colorant "Shikon color," a commercial root extract from Lithospermum erythrorhizon SIEBOLD et ZUCCARINI. The structure of tigloylshikonin was elucidated using 1H, 13C, the difference nuclear Overhauser effect (NOE), and 2D NMR techniques. Its stereochemistry was determined by chiral-phase HPLC analysis. Tigloylshikonin was also found in the roots of L. erythrorhizon, which indicated that this new shikonin derivative is a typical component of naphthoquinone pigments in the roots of L. erythrorhizon.
- Ito, Yusai,Onobori, Kenichi,Yamazaki, Takeshi,Kawamura, Yoko
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experimental part
p. 117 - 119
(2011/02/28)
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- An efficient improvement on total synthesis of shikonin
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The problem associated with electrolytic deprotection, which is a concern in the total synthesis of shikonin, is solved by the addition of Cu2+ to the electrolysis system. The improvement has three advantages: first, it practically increased the yield from 40 to 85%; second, the isolation of shikonin became much easier. Third, the reaction time was significantly shortened.
- Rao, Zhen,Zhou, Wen,Peng, Ying,Li, Shao-Shun
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experimental part
p. 236 - 237
(2010/08/06)
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- Human ACAT inhibitory effects of shikonin derivatives from Lithospermum erythrorhizon
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Three naphthoquinones were isolated by bioassay-guided fractionation from the CHCl3 extracts of roots of Lithospermum erythrorhizon. They were identified as acetylshikonin (1), isobutyrylshikonin (2), and β-hydroxyisovalerylshikonin (3) on the basis of their spectroscopic analyses. The compounds 1-3 were tested for their inhibitory activities against human ACAT-1 (hACAT-1) or human ACAT-2 (hACAT-2). Compound 2 preferentially inhibited hACAT-2 (IC50 = 57.5 μM) than hACAT-1 (32% at 120 μM), whereas compounds 1 and 3 showed weak inhibitory activities in both hACAT-1 and -2. To develop more potent hACAT inhibitor, shikonin derivatives (5-11) were synthesized by semi-synthesis of shikonin (4), which was prepared by hydrolysis of 1-3. Among them, compounds 5 and 7 exhibited the strong inhibitory activities against hACAT-1 and -2. Furthermore, we demonstrated that compound 7 behaved as a potent ACAT inhibitor in not only in vitro assay system but also cell-based assay system.
- An, Sojin,Park, Yong-Dae,Paik, Young-Ki,Jeong, Tae-Sook,Lee, Woo Song
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p. 1112 - 1116
(2007/10/03)
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- A new efficient route for multigram asymmetric synthesis of alkannin and shikonin
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A short and convergent approach for the synthesis of alkannin, shikonin and shikalkin is presented. A Hauser-type annulation of cyanophthalide 26 with enone 7 affords the complete aromatic system in just one step with concomitant attachment of the entire side chain. Subsequent Corey's oxazaborolidine mediated asymmetric reduction of the above advanced intermediate, leads to the required isomer in high enantiomeric excess. Finally, a selective and high yielding deprotection protocol furnishes the title compounds as pure crystalline precipitates. Thus, a multigram synthesis of shikonin, alkannin and shikalkin is achieved in high yield and enantioselectivity.
- Couladouros, Elias A.,Strongilos, Alexandros T.,Papageorgiou, Vassilios P.,Plyta, Zoi F.
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p. 1795 - 1803
(2007/10/03)
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- Concise and efficient total syntheses of alkannin and shikonin
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Two enantiomic natural products with wound-healing properties, alkannin (1) and shikonin (2), are accessible by a short and efficient total synthesis. The success was achieved by a novel protecting system for masking of 5,8-dihydroxy-1,4-naphthoquinones (naphthazarins) and a highly stereoselective ketone reduction.
- Nicolaou,Hepworth, David
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p. 839 - 841
(2007/10/03)
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- Synthesis of dl-shikonin by vanadium(II)-assisted cross-coupling and electrooxidation of aromatic nuclei
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Vanadium(II)-assisted cross-coupling of 1,4,5,8-tetramethoxynaphthalene-2-carbaldehyde and 3-methyl-2-butenal was employed for introduction of the side chain of dl-shikonin. 2-(1-Hydroxy-4-methyl-3-pentenyl)-1,4,5,8-tetramethoxynaphthalene was prepared by the pinacol coupling and the subsequent palladium-catalyzed hydrogenolysis of the carbon-oxygen bond at the allylic position of the diol carbonate. Electrochemical oxidation of the 2-substituted 1,4,5,8-tetramethoxynaphthalene, followed by reductive acetylation with zinc and the subsequent electrooxidation of the resulting 5,8-diacetoxy-1,4-dimethoxynaphthalene, afforded the corresponding 5,8-diacetoxy-1,4-naphthoquinone, whose alkaline hydrolysis furnished dl-shikonin.
- Torii,Akiyama,Yamashita,Inokuchi
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p. 2917 - 2922
(2007/10/03)
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- SYNTHESIS OF SHIKALKIN AND CERTAIN RALATED COMPOUNDS
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A successful total synthesis of a biologically active pigment from plants of the Boraginaceae family was carried out with naphthazarine as the starting material, and using the 1,4,5,8-tetramethoxynaphthalene, the corresponding 2-vinyl derivative and its epoxide or a cyclopropane adduct with diazoacetic ester at the key stages.In the course of developing the scheme of the synthesis of shikalkin, its three analogs were obtained, differing in the nature of the monoterpenoid side chain. Keywords: shikonin, alkannin, shikalkin, naphthazarine, tetramethoxynaphthalene, olefinization according to Wittig, cyclopropyl-carbinylic rearrangement, cerium-ammonium nitrate.
- Novikov, V. L.,Balaneva, N. N.,Moiseenkov, A. M.,Elyakov, G. B.
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p. 1485 - 1494
(2007/10/02)
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- Synthesis of Shikonin and Alkannin
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The enantiomeric naturally occurring naphthoquinones shikonin and alkannin have been synthesized in a thirteen-step procedure in 44 to 65percent e.e.The stereogenic centers of (R)-1 and (S)-1 are created by the reaction of naphthaldehyde 3 with (R)- and (S)-2-hydroxy-1,2,2-triphenylethyl acetate (2), respectively.In order to find out a rationalization for the unexpectedly low diastereoselectivity in this aldol addition, a series of substituted aromatic aldehydes 12a-h has been treated with (R)-2. Key words: Naphthoquinone / Aldol addition / (R)-Shikonin / (S)-Alkannin
- Braun, Manfred,Bauer, Claus
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p. 1157 - 1164
(2007/10/02)
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- Total Synthesis of Shikalkin
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The first total syntheses of dihydroshikalkin and shikalkin were accomplished.
- Terada, Akira,Tanoue, Yasuhiro,Hatada, Akira,Sakamoto, Hiroshi
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p. 987 - 988
(2007/10/02)
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