Preparation of 8-methyl-2-decanol: General synthesis of diastereomeric mixtures of alkyl branched insect pheromones
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry,Ecology, Evolution, Behavior and Systematics,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF01013241.pdf
Reference19 articles.
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2. Abrams, S.R. 1982. Isomerization of acetylenic acids with sodium salt of 1,2-diaminoethane: A one-step synthesis of megatomoic acid.Can. J. Chem. 60:1238?1243.
3. Abrams, S.R., andShaw, A.C. 1985. Deuteration of cycloalkynes.Tetrahedron Lett. 26:3431?3432.
4. Abrams, S.R., andShaw, A.C. 1986. Triple bond isomerizations.Org. Synth. 2377: In press.
5. Brown, C.A., andYamashita, A. 1975. The acetylene zipper. An exceptionally facile ?contra-thermodynamic? multipositional isomerization of alkynes with potassium 3-aminopropylamide.J. Am. Chem. Soc. 97:891?892.
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2. A general approach to enantiomerically pure methylcarbinols. Asymmetric synthesis of antibiotic (-)-A26771B and the WCR sex pheromone;The Journal of Organic Chemistry;1993-12
3. Synthesis of two stereoisomers of the propanoate ester of 8-methyl-2-decanol using remote asymmetric induction;Tetrahedron;1990-01
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