5,7-Cholestadien-3 beta-ol was transformed into 14 beta-cholesta-5,7-dien-3 beta-ol in six steps. The inversion of the stereochemistry at C-14 was obtained by a selective protection of the delta 5 and the elaboration of the delta 7 double bond.

Synthesis of 14 beta-cholesta-5,7-dien-3 beta-ol / M. Anastasia, P. Allevi, P. Ciuffreda, A. Fiecchi, A. Scala. - In: STEROIDS. - ISSN 0039-128X. - 49:6(1987), pp. 543-552.

Synthesis of 14 beta-cholesta-5,7-dien-3 beta-ol

M. Anastasia;P. Allevi;P. Ciuffreda;A. Scala
1987

Abstract

5,7-Cholestadien-3 beta-ol was transformed into 14 beta-cholesta-5,7-dien-3 beta-ol in six steps. The inversion of the stereochemistry at C-14 was obtained by a selective protection of the delta 5 and the elaboration of the delta 7 double bond.
Settore BIO/10 - Biochimica
STEROIDS
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

Caricamento pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/185086
Citazioni
  • ???jsp.display-item.citation.pmc??? 0
  • Scopus 4
  • ???jsp.display-item.citation.isi??? ND
social impact