Heterocyclic Steroids .7. Rearrangement Of 1-Diethylamino-5-(Met-Methoxyphenoxy)-Pent-2-Yne


Autoria(s): Kasturi, TR; Govindan, G; Damodaran, KM; Subrahma, G
Data(s)

1973

Resumo

Thermal rearrangement of diethylamino5-(m methoxyphenoxy)-pent-2-yne (3) gives 1-(m-methexyphenoxy)-pent-3,4-diene (14) in about 8% yield. Hydration of the latter yields 1-(m-methoxyphenoxy)-pentan-4-one (6), which has been synthesised by an unambiguous route. A mechanism of formation of the allene (14) from the amine (3) has been suggested.

Formato

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Identificador

http://eprints.iisc.ernet.in/28839/1/12sdarticle.pdf

Kasturi, TR and Govindan, G and Damodaran, KM and Subrahma, G (1973) Heterocyclic Steroids .7. Rearrangement Of 1-Diethylamino-5-(Met-Methoxyphenoxy)-Pent-2-Yne. In: Tetrahedron, 29 (5). pp. 715-718.

Publicador

Elsevier Science

Relação

http://dx.doi.org/10.1016/0040-4020(73)80083-3

http://eprints.iisc.ernet.in/28839/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed