Useful synthetic reagents derived from 1-triisopropylsilylpropyne and 1,3-[triisopropylsilyl]propyne, direct, stereoselective synthesis of either or enynes
- 1 January 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (7) , 719-722
- https://doi.org/10.1016/s0040-4039(00)86930-0
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Stereoselective carbonyl-olefination via organosilicon compoundsJournal of the American Chemical Society, 1981
- Asymmetric synthesis of hydroxycarboxylic acidsThe Journal of Organic Chemistry, 1981
- Direct evidence supporting a single electron transfer pathway in the reduction of ketones by primary, secondary, and tertiary Grignard reagentsJournal of the American Chemical Society, 1981
- Silanes in organic syuthesis. 11. Regiocontrolled synthesis of α-hydroxymethylated (trimethylsilyl)allenesTetrahedron Letters, 1981
- Organometallic reaction mechanisms. 15. Factors influencing the nature of Grignard reactions with ketonesJournal of the American Chemical Society, 1978
- Synthetic route to neurotoxins in the 2,7--histrionicotoxin seriesTetrahedron Letters, 1975
- Simple total synthesis of (+-)-perhydrohistrionicotoxinJournal of the American Chemical Society, 1975
- Stereoselective methods for the synthesis of terminal and enyne unitsTetrahedron Letters, 1973
- Reaction of the Grignard reagent from neopentyl chloride with benzophenone. Nuclear magnetic resonance study.The Journal of Organic Chemistry, 1969
- Position-specific alkylation of lithio-1-trimethylsilylpropyne, a useful new route to acetylenes and 1, 5-dienesTetrahedron Letters, 1968