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Reaction of copper enolates of esters with propargylic systems. Facile preparation of 3,4-dienoic esters, stereoselective rearrangement to (2E,4Z)- and (2E,4E)-dienoic esters, and stereoselective synthesis of a fragrance from the Bartlett pear
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Reaction of copper enolates of esters with propargylic systems. Facile preparation of 3,4-dienoic esters, stereoselective rearrangement to (2E,4Z)- and (2E,4E)-dienoic esters, and stereoselective synthesis of a fragrance from the Bartlett pear
Reaction of copper enolates of esters with propargylic systems. Facile preparation of 3,4-dienoic esters, stereoselective rearrangement to (2E,4Z)- and (2E,4E)-dienoic esters, and stereoselective synthesis of a fragrance from the Bartlett pear
RA
Richard A. Amos
Richard A. Amos
JK
John A. Katzenellenbogen
John A. Katzenellenbogen
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1 February 1978
journal article
research article
Published by
American Chemical Society (ACS)
in
The Journal of Organic Chemistry
Vol. 43
(4)
,
555-560
https://doi.org/10.1021/jo00398a006
Abstract
No abstract available
Cited by 56 articles