Asymmetric synthesis of steroidal Tröger's base analogues. X-Ray molecular structure of methyl 3?,12?-{6H,12H-5,11-methanodibenzo[b,f][1,5]diazocine-2,8-bisacetoxy}-5?-cholan-24-oate


Autoria(s): Uday, Maitra; Braja, Gopal Bag; Rao, Photon; Powell, Douglas
Data(s)

21/08/1995

Resumo

Cyclization of compound 5c in trifluoroacetic acid/hexamethylenetetramine produces Tröger's base analogue 6c in 75% yield with 70% diastereoselectivity.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/36937/1/steroida.pdf

Uday, Maitra and Braja, Gopal Bag and Rao, Photon and Powell, Douglas (1995) Asymmetric synthesis of steroidal Tröger's base analogues. X-Ray molecular structure of methyl 3?,12?-{6H,12H-5,11-methanodibenzo[b,f][1,5]diazocine-2,8-bisacetoxy}-5?-cholan-24-oate. In: Perkin Transactions 1 (16). pp. 2049-2056.

Publicador

Royal Society of Chemistry

Relação

http://pubs.rsc.org/en/Content/ArticleLanding/1995/p1/P19950002049

http://eprints.iisc.ernet.in/36937/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed