Regio- and stereo-chemical features of the stannylcopper(I)-induced substitution in propargylic substrates
- 1 January 1983
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 241 (3) , 417-422
- https://doi.org/10.1016/s0022-328x(00)98533-4
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Stereospecific synthesis of vinylstannanes using triphenylstannycopper(I) species. preparation of the cis-isomer of the presumed sex attractant of acanthoscelides obtectus.Tetrahedron Letters, 1982
- Reaction of trimethyl- and triphenylstannate, (CH3)3Sn- and Ph3Sn-, with optically active 2-octyl bromide, chloride, and tosylateJournal of the American Chemical Society, 1982
- Unambiguous determination of the stereochemistry of methylcopper and lithium tetranydridoaluminate-induced allene formation in the steroid series. A revision of literature dataJournal of the Chemical Society, Chemical Communications, 1982
- Reaction of (trimethylstannyl) copper reagents with α, β-acetylenic estersTetrahedron Letters, 1981
- Ag(I)-assisted hydrolysis of mestranol methanesulfonate into epimestranolTetrahedron Letters, 1980
- Application of allenylsilver(I) compounds in organic synthesis. A simple route to substituted allenesJournal of Organometallic Chemistry, 1980
- Preferred - 1,3- substitution by attack of organocuprates on the methane—sulfinate of (R)-(−)-3-hydroxy-3-phenylpropyne. An attractive route to chiral allenes.Tetrahedron Letters, 1978
- A new synthesis of allenic hydrocarbons from tertiary 2‐propynyl sulfinates and organocopper(I) compounds. Evidence for a syn‐l,3‐substitution pattern in the steroid seriesRecueil des Travaux Chimiques des Pays-Bas, 1978