936638-45-8Relevant academic research and scientific papers
Stereocontrol in palladium-catalyzed propargylic substitutions: Kinetic resolution to give enantioenriched 1,5-enynes and propargyl acetates
Ardolino, Michael J.,Eno, Meredith S.,Morken, James P.
supporting information, p. 3413 - 3419 (2013/12/04)
Kinetic resolution during the catalytic allyl-propargyl cross-coupling with chiral starting materials can be accomplished with a chiral palladium catalyst. These reactions offer ready access to enantiomerically enriched enyne products from simple, readily
Chlorocyclopropane macrolides from the marine sponge Phorbas sp. assignment of the configurations of phorbasides A and B by quantitative CD
Skepper, Colin K.,MacMillan, John B.,Zhou, Guang-Xiong,Masuno, Makoto N.,Molinski, Tadeusz F.
, p. 4150 - 4151 (2008/02/04)
Two new chlorocyclopropane macrolides, phorbasides A and B, have been characterized from the sponge Phorbas sp. that previously yielded phorboxazoles A and B. We describe the assignment of the absolute configuration of the trans-chlorocyclopropane ring th
