On the Stereospecific Conversion of Proximally-Oxygenated Trisubstituted Vinyltriphenylstannanes into Stereodefined Trisubstituted Alkenes
Author:
Affiliation:
1. The Christopher Ingold Laboratories, The Chemistry Department, University College London, 20 Gordon Street, London WC1H 0AJ, United Kingdom
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol051935t
Reference22 articles.
1. O-Directed Free-Radical Hydrostannations of Propargyl Ethers, Acetals, and Alcohols with Ph3SnH and Et3B
2. Mechanistic Studies on the O-Directed Free-Radical Hydrostannation of Disubstituted Acetylenes with Ph3SnH and Et3B and on the Iodination of Allylically Oxygenated α-Triphenylstannylalkenes
3. Transition Metal-Assisted Transformations of Diversely Functionalized Dienynes
4. Intramolecular O.fwdarw.Sn coordination in (Z)-17-[2-(triphenylstannyl)vinyl]-4-estren-17-ol: evidence by x-ray diffraction analysis and iodo demetalation
5. In vitro effect of organotin-substituted steroids in human tumor cell lines
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