Aspects of tautomerism. 13. Alkaline hydrolysis of .gamma.-, .delta.-, and .epsilon.-keto esters and their desoxy analogs. Geometrical constraints on keto participation


Autoria(s): Bhatt, Vivekananda M; Ravindranathan, M; Somayaji, Viswanatha; Rao, Venkoba G
Data(s)

1984

Resumo

The rates of alkaline hydrolysis of methyl &benzoylpropionate (I), methyl y-benzoylbutyrate (11) and methyll6-benzoylvalerate (In) decrease in the order I > I1 > III. Keto participation is the predominant pathway in the case of y-keto esters. Evidence has also been obtained for keto participation in the case of 6-keto esters, whereas no such evidence is available in the case of r-keto esters studied.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/22356/1/6fulltext.pdf

Bhatt, Vivekananda M and Ravindranathan, M and Somayaji, Viswanatha and Rao, Venkoba G (1984) Aspects of tautomerism. 13. Alkaline hydrolysis of .gamma.-, .delta.-, and .epsilon.-keto esters and their desoxy analogs. Geometrical constraints on keto participation. In: Journal of Organic Chemistry, 49 (7). pp. 3170-3173.

Publicador

American Chemical Society

Relação

http://pubs.acs.org/doi/abs/10.1021/jo00191a024

http://eprints.iisc.ernet.in/22356/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed