A novel anionic rearrangement of a cyclohexadienone. A serendipitous synthesis of methyl (E)-3-Isopropyl-6-oxohept-4-enoate

Carman R.M. and Van Dongen J.M.A.M. (1985) A novel anionic rearrangement of a cyclohexadienone. A serendipitous synthesis of methyl (E)-3-Isopropyl-6-oxohept-4-enoate. Australian Journal of Chemistry, 39 12: 2171-2175. doi:10.1071/CH9862171


Author Carman R.M.
Van Dongen J.M.A.M.
Title A novel anionic rearrangement of a cyclohexadienone. A serendipitous synthesis of methyl (E)-3-Isopropyl-6-oxohept-4-enoate
Journal name Australian Journal of Chemistry   Check publisher's open access policy
ISSN 1445-0038
Publication date 1985
Sub-type Article (original research)
DOI 10.1071/CH9862171
Volume 39
Issue 12
Start page 2171
End page 2175
Total pages 5
Subject 1600 Chemistry
Abstract The cyclohexadienone (2b) with methanolic potassium hydroxide provides the two isomeric cyclopentenecarboxylic acid derivatives (5) and (6) together with the acyclic ester (4a).
Q-Index Code C1
Q-Index Status Provisional Code
Institutional Status Unknown

Document type: Journal Article
Sub-type: Article (original research)
Collection: Scopus Import
 
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