316377-63-6Relevant articles and documents
Synthetic studies on the trans-chlorocyclopropane dienyne side chain of callipeltoside A.
Olivo,Velazquez,Trevisan
, p. 4055 - 4058 (2007/10/03)
[structure] Enantiomerically enriched trans-chlorocyclopropanemethanol was obtained by lipase kinetic resolution of dichlorocyclopropanemethanol 3, followed by reduction. The sp-sp(2) bond of the trans-chlorocyclopropane dienyne side chain of callipeltoside A was constructed via a Stille coupling reaction of 1, 1-dibromo-1-alkene 7 and a vinylstannane in a highly dipolar solvent capable of promoting HBr elimination to give internal alkynes.