587875-56-7Relevant articles and documents
Synthesis of diacetal trioxa-cage compounds via reaction of bicyclo[2.2.1]heptenes and bicyclo[2.2.2]octenes with dimethyldioxirane
Lin, Hui-Chang,Wu, Hsien-Jen
, p. 341 - 350 (2007/10/03)
A new entry for the synthesis of diacetal trioxa-cage compounds via oxirane-induced sequential cyclization reaction of 2,3-bis-endo- diacylbicyclo[2.2.1]-5-heptenes and 2,3-bis-endo-diacylbicyclo[2.2.2]-5- octenes is reported. In the case of bicyclo[2.2.2]octenes, sequential cyclization reaction induced by iodine as electrophile failed. We have also demonstrated that dimethyldioxirane can selectively oxidize hemiacetals to give lactones with the secondary hydroxy group intact. (C) 2000 Elsevier Science Ltd.
Asymmetrization of a meso 1,2-enediol bis(trimethylsilyl) ether using a (S)-BINOL monoisopropyl ether(BINOL-Pr(i))-tin tetrachloride complex: An alternative route to (-)-ketodicyclopentadiene and (-)-ketotricyclononene
Taniguchi, Takahiko,Ogasawara, Kunio
, p. 6429 - 6432 (2007/10/03)
A tricyclic mesa 12-enediol bis(trimethylsilyl) ether having an endo-tricyclo[4.2.1.02,5]nonene framework has been asymmetrically desymmetrized by protonation with a complex generated from (S)-BINOL monoisopropyl ether (BINOL-Pr(i)) and tin tetrachloride to give the optically enriched acyloin in 90% ee. The chiral acyloin thus obtained has been transformed into two versatile chiral building blocks, (-)-ketodicyclopentadiene and (-)-ketotricyclononene, in optically pure forms via a sequence involving concurrent enzymatic acetylation and optical purification.
Lipase-triethylamine-mediated dynamic transesterification of a tricyclic acyloin having a latent meso-structure: A new route to optically pure oxodicyclopentadiene
Taniguchi, Takahiko,Ogasawara, Kunio
, p. 1399 - 1400 (2007/10/03)
The racemic tricyclic acyloin (±)-endo-3-hydroxytricyclo[4.2.1.02,5]non-7-en-4-one has been dynamically resolved via the transient formation of the meso-enediol isomer under lipase-triethylamine-mediated kinetic transesterification conditions to give the single chiral acetate (-)-endo-3-acetoxytricyclo[4.2.1.02,5]non-7-en-4-one, serving as a precursor of (-)-oxodicyclopentadiene, in excellent optical and chemical yields.
First exclusive regioselective fragmentation of primary ozonides controlled by remote carbonyl groups and a new method for determining the regiochemistry of carbonyl oxide formation
Wu, Hsien-Jen,Lin, Chu-Chung
, p. 3820 - 3828 (2007/10/03)
The first exclusive regioselective fragmentation of primary ozonides controlled by remote carbonyl groups on ozonolysis of norbornene derivatives and reaction of final ozonides with triethylamine as a new probe for determining the regiochemistry of carbonyl oxide formation from primary ozonide fragmentation are reported. Ozonolysis of the endo adducts 3a-d and the deuterated compounds 8a and 8b in CDCl3 at -78°C gave the final ozonides 4a-d, 9a, and 9b as the sole products (>95%), respectively. No detectable amount of the isomeric final ozonides 5, 10, 11, and 12 was obtained. A mechanism is proposed to account for the exclusive regioselective fragmentation of the primary ozonides. Ozonolysis of 3a-d, 8a, and 8b in CH2Cl2 at -78°C followed by treatment with triethylamine exclusively gave the convex tetraquinane oxa cage compounds 16a-d, 19a, and 19b in 85-90% yields, respectively. No detectable amount of the other regioisomers 17a-d, 20a, and 20b was obtained. Ozonolysis of 3a-d, 8a, and 8b in CH2Cl2 at -78°C followed by reduction with dimethyl sulfide gave the tetraacetal tetraoxa cage compounds 21a-d, 23a, and 23b in 85% yields, respectively. The difference in function between triethylamine and dimethyl sulfide in reaction with final ozonide is demonstrated. Ozonolysis of the endo adducts 24a and 24b in CDCl3 at -78°C exclusively gave the final ozonides 27a and 27b, respectively. The order of the preference of various remote carbonyl groups to control the fragmentation of the primary ozonides formed by ozonolysis of norbornene derivatives is investigated. Ozonolysis of the endo esters 32a-c in CH2Cl2 at -78°C followed by reduction with dimethyl sulfide gave the new tetraacetal oxa cages 35a-c, with an alkoxyl group directly on the skeleton, and the novel triacetal oxa cages 36b and 36c, respectively. The structures of triacetal oxa cages are proven for the first time by X-ray analysis of the crystalline compound 36c.
