bakkenolide-a and cyclohexene

bakkenolide-a has been researched along with cyclohexene* in 1 studies

Other Studies

1 other study(ies) available for bakkenolide-a and cyclohexene

Article	Year
First comprehensive bakkane approach: stereoselective and efficient dichloroketene-based total syntheses of (+/-)- and (-)-9-acetoxyfukinanolide, (+/-)- and (+)-bakkenolide A, (-)-bakkenolides III, B, C, H, L, V, and X, (+/-)- and (-)-homogynolide A, (+/- Journal of the American Chemical Society, 2002, Dec-25, Volume: 124, Issue:51 Cycloaddition of dichloroketene with dimethylcyclohexenes has been used as the key reaction in an efficient, general approach to the bakkanes. New methods and methodologies that have been developed in this work include spiro beta-methylene-gamma-butyrolactonizations, a vicinal dicarboxylation, an angelic ester preparation, a transesterification, an epoxy ketone double reduction, and a retro aldol-aldol approach to low-energy aldol isomers. Topics: 4-Butyrolactone; Cyclohexanes; Cyclohexenes; Dichloroethylenes; Petasites; Sesquiterpenes; Stereoisomerism	2002

Article

Year

First comprehensive bakkane approach: stereoselective and efficient dichloroketene-based total syntheses of (+/-)- and (-)-9-acetoxyfukinanolide, (+/-)- and (+)-bakkenolide A, (-)-bakkenolides III, B, C, H, L, V, and X, (+/-)- and (-)-homogynolide A, (+/-

Journal of the American Chemical Society, 2002, Dec-25, Volume: 124, Issue:51

Cycloaddition of dichloroketene with dimethylcyclohexenes has been used as the key reaction in an efficient, general approach to the bakkanes. New methods and methodologies that have been developed in this work include spiro beta-methylene-gamma-butyrolactonizations, a vicinal dicarboxylation, an angelic ester preparation, a transesterification, an epoxy ketone double reduction, and a retro aldol-aldol approach to low-energy aldol isomers.

Topics: 4-Butyrolactone; Cyclohexanes; Cyclohexenes; Dichloroethylenes; Petasites; Sesquiterpenes; Stereoisomerism

2002