dolabelide-c and divinyl-sulfone

dolabelide-c has been researched along with divinyl-sulfone* in 1 studies

Other Studies

1 other study(ies) available for dolabelide-c and divinyl-sulfone

Article	Year
Tandem conjugate addition-elimination for the diastereoselective synthesis of 4E-alkenyl syn-1,3-diols. Organic letters, 2007, Oct-11, Volume: 9, Issue:21 We have developed a tandem conjugate addition-elimination sequence for the diastereoselective synthesis of protected allylic syn-1,3-diols, starting from vinyl sulfones. The sulfonyl group was then reduced with sodium amalgam to furnish the E-olefin as the major isomer. This method was applied to the synthesis of a trisubstituted alkene modeling the C21-C25 fragment of Dolabelide C. Topics: Alcohols; Alkenes; Diterpenes; Macrolides; Molecular Structure; Stereoisomerism; Sulfones	2007

Article

Year

Tandem conjugate addition-elimination for the diastereoselective synthesis of 4E-alkenyl syn-1,3-diols.

Organic letters, 2007, Oct-11, Volume: 9, Issue:21

We have developed a tandem conjugate addition-elimination sequence for the diastereoselective synthesis of protected allylic syn-1,3-diols, starting from vinyl sulfones. The sulfonyl group was then reduced with sodium amalgam to furnish the E-olefin as the major isomer. This method was applied to the synthesis of a trisubstituted alkene modeling the C21-C25 fragment of Dolabelide C.

Topics: Alcohols; Alkenes; Diterpenes; Macrolides; Molecular Structure; Stereoisomerism; Sulfones

2007