Literature DB >> 12762777

Optimization of the abnormal Beckmann rearrangement: application to steroid 17-oximes.

Cunde Wang1, Xin Jiang, Haijian Shi, Jun Lu, Yuefei Hu, Hongwen Hu.   

Abstract

A novel and practical procedure was developed for the abnormal Beckmann rearrangement of steroid 17-oximes. Treatment of the 17-oximes with TFA/CH(OMe)(3) in boiling THF for 2 h gives the corresponding 13,17-seco alkene nitrile products in unprecedented high yields (70-92%). Since the alkene nitriles can be subsequently converted into 18-norsteroids, this general method provides a highly efficient route to these biologically important compounds and, by extension, to other structurally related natural products.

Entities:  

Year:  2003        PMID: 12762777     DOI: 10.1021/jo034142y

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Neurosteroid Analogues. 13. Synthetic methods for the preparation of 2beta-hydroxygonane derivatives as structural mimics of ent-3alpha-hydroxysteroid modulators of GABA(A) receptors.

Authors:  Cunde Wang; Nigam P Rath; Douglas F Covey
Journal:  Tetrahedron       Date:  2007-08-13       Impact factor: 2.457

  1 in total

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