Studies in stereochemistry—I : Stereospecific routes to trans- anti- and cis- syn-Δ8-dodecahydrophenanthrenes


Autoria(s): Balasubramanian, SK
Data(s)

1961

Resumo

Reduction of trans-1-oxo-7-methoxy-1,2,3,4,9,10,11,12-octahydrophenanthrene (XI) by lithium tri-t-butoxyaluminohydride gave trans-1β-hydroxy-7-methoxy-1,2,3,4,9,10,11,12-octahydrophenanthrene (XII) which on lithium-liquid ammonia reduction gave trans-anti-1β-hydroxy-7-oxo-Δ8(14)-dodecahydrophenanthrene (XIII). Reduction of cis-1-oxo-7-methoxy-1,2,3,4,9,10,11,12-octahydrophenanthrene (XV) by sodium borohydride gave cis-1α-hydroxy-7-methoxy-1,2,3,4,9,10,11,12-octahydrophenanthrene (XVI) which on lithium-liquid ammonia reduction gave cis-syn-1α-hydroxy-7-oxo-Δ8(14)-dodecahydrophenanthrene (XVII).

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/28437/1/SYN.pdf

Balasubramanian, SK (1961) Studies in stereochemistry—I : Stereospecific routes to trans- anti- and cis- syn-Δ8-dodecahydrophenanthrenes. In: Tetrahedron, 12 (4). pp. 196-204.

Publicador

Elsevier Science

Relação

http://dx.doi.org/10.1016/0040-4020(61)80034-3

http://eprints.iisc.ernet.in/28437/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed