Literature DB >> 538775

Improved preparation of pregn-5-ene-3 beta,16 alpha,20-triols and 5 alpha-pregnane-3 alpha,16 alpha,20-triols.

D N Kirk, M L Sá e Melo.   

Abstract

The compounds named in the title were prepared by routes which included the reduction of suitable 16 alpha,17-epoxypregnan-20-ones with aluminium amalgam to give 16 alpha-hydroxypregnan-20-ones, and reduction of the 20-oxo function either with sodium borohydride to obtain the 3,16 alpha,20 beta-triols or with lithium-liquid ammonia to obtain the 3,16 alpha,20 alpha-triols.

Entities:  

Mesh:

Substances:

Year:  1979        PMID: 538775     DOI: 10.1016/0039-128x(79)90138-7

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  1 in total

1.  Structure elucidation of two isomeric steroids: photolytical and thermal reaction products from norethisterone studied by two-dimensional nuclear magnetic resonance.

Authors:  A G Sedee; G M Beijersbergen van Henegouwen; W Guijt; C A Haasnoot
Journal:  Pharm Weekbl Sci       Date:  1985-10-25
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.