pachastrissamine and allyl-alcohol

pachastrissamine has been researched along with allyl-alcohol* in 1 studies

Other Studies

1 other study(ies) available for pachastrissamine and allyl-alcohol

ArticleYear
Substrate and stereocontrolled iodocycloetherification of highly functionalized enantiomerically pure allylic alcohols: application to synthesis of cytotoxic 2-epi jaspine B and its biological evaluation.
    Organic & biomolecular chemistry, 2015, Aug-14, Volume: 13, Issue:30

    Stereoselectivities of electrophilic additions of molecular iodine to enantiomerically pure highly functionalized allylic alcohols with internal nucleophiles have been investigated. The intramolecular nucleophilic attack on the I2-π complex by an oxygen nucleophile to obtain tri- and tetrasubstituted THFs is highly regio-, stereoselective and substrate controlled. The application of this study has been shown by utilizing one of the THFs 4a as a key intermediate to complete the total synthesis of marine anti-cancer natural product 2-epi jaspine B.

    Topics: Cell Death; Cell Line, Tumor; Cell Proliferation; Cyclization; Ethers; Humans; Inhibitory Concentration 50; Iodides; Magnetic Resonance Spectroscopy; Molecular Conformation; Propanols; Sphingosine; Stereoisomerism

2015