| Literature DB >> 23741206 |
Abstract
A propargylic ester containing a propargylic alkoxy group has been observed to preferentially undergo [1,2]-acyl shift over [1,3]-shift. In addition, the complementary and contrasting reactivity of vinyl vs. alkynyl platinum carbenoids has been discovered. Vinyl Pt-carbenoids are more prone to undergo [1,2]-H shift over addition to π-bonds whereas alkynyl Pt-carbenoids preferentially add to π-bonds.Entities:
Keywords: alkynes; carbenoids; cyclopropanes; platinum; substituent effects
Year: 2008 PMID: 23741206 PMCID: PMC3670796 DOI: 10.1002/adsc.200800544
Source DB: PubMed Journal: Adv Synth Catal ISSN: 1615-4150 Impact factor: 5.837