A Novel Synthesis of 2,6‐Diolefinic Esters: Ethyl and methyl trans‐2,cis‐6‐dodecadienoate, two Bartlett pear constituents
- 31 January 1972
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 55 (1) , 82-85
- https://doi.org/10.1002/hlca.19720550112
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Stereospecific Olefin Synthesis via Lithium VinylcupratesHelvetica Chimica Acta, 1971
- Volatile components of Bartlett pear. High boiling estersJournal of Agricultural and Food Chemistry, 1970
- Conjugate addition reactions with lithium diallylcuprateThe Journal of Organic Chemistry, 1969
- Reaction of lithium dialkyl- and diarylcuprates with organic halidesJournal of the American Chemical Society, 1969
- Synthese von 7α‐Methylöstron. Über Steroide, 210. MitteilungHelvetica Chimica Acta, 1967
- Volatile Components of Bartlett Pear. V.Journal of Food Science, 1966
- Volatile Esters of Bartlett Pear. IV. Esters of Trans:2‐cis:4‐decadienoic AcidaJournal of Food Science, 1964
- Volatile Esters of Bartlett Pear. III.aJournal of Food Science, 1964
- Volatile Esters of Bartlett Pear. II.Journal of Food Science, 1963
- Synthese und Stereochemie der isomeren AmbrinoleHelvetica Chimica Acta, 1959