Reaction of spironaphthalenones with hydroxylamine: Part II. Structure of product in the reaction of 1′-substituted spironaphthalenone.


Autoria(s): Kasturi, Tirumalai R; Kumar, Kaipenchery A; Pragnacharyulu, Palle VP
Data(s)

01/01/1993

Resumo

Reaction of 1′-aryl substituted spironaphthalenones 1a–d with hydroxylamine hydrochloride in ethanol gave substituted cinnamic ester derivatives 4a–d. Similarly, reaction of spironaphthalenone 1a with different alcohols gave the corresponding esters 4i–m. Reaction of unsymmetrical spironaphthalenones 1e–h with hydroxylamine hydrochloride in presence of ethanol gave the respective esters 4e–h. All the esters were characterised by their spectral data.

Formato

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Identificador

http://eprints.iisc.ernet.in/35723/1/Reaction2.pdf

Kasturi, Tirumalai R and Kumar, Kaipenchery A and Pragnacharyulu, Palle VP (1993) Reaction of spironaphthalenones with hydroxylamine: Part II. Structure of product in the reaction of 1′-substituted spironaphthalenone. In: Tetrahedron, 49 (1). pp. 125-134.

Publicador

Elsevier Science

Relação

http://dx.doi.org/10.1016/S0040-4020(01)80512-3

http://eprints.iisc.ernet.in/35723/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed