Stereospecific synthesis of a biologically active dehydro derivative of the C18-juvenile hormone of cecropia. New routes to a key C12-intermediate
- 1 January 1971
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 12 (21) , 1821-1824
- https://doi.org/10.1016/s0040-4039(01)87471-2
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Simple, stereospecific syntheses of C17- and C18- Cecropia juvenile hormones (racemic) from a common intermediateJournal of the American Chemical Society, 1970
- A Stereospecific Total Synthesis of α-SantalolJournal of the American Chemical Society, 1970
- Stereospecific total synthesis of the dl-C18 Cecropia juvenile hormoneJournal of the American Chemical Society, 1968
- Carbon-carbon bond formation by selective coupling of n-alkylcopper reagents with organic halidesJournal of the American Chemical Society, 1968
- Position-specific alkylation of lithio-1-trimethylsilylpropyne, a useful new route to acetylenes and 1, 5-dienesTetrahedron Letters, 1968
- New stereospecific synthesis of trisubstituted olefins. Stereospecific synthesis of farnesolJournal of the American Chemical Society, 1967
- Selective formation of carbon-carbon bonds between unlike groups using organocopper reagentsJournal of the American Chemical Society, 1967
- Studies on the biosynthesis of cholesterol. 5. Biosynthesis of squalene from dl-3-hydroxy-3-methyl-[2–14C]pentano-5-lactoneBiochemical Journal, 1958
- 651. Carotenoids and related compounds. Part I. Total synthesis of “all-trans”-methylbixin and of a diketone with the capsorubin chromophoreJournal of the Chemical Society, 1953