Literature DB >> 15631862

The stereochemistry of the Grignard reaction of steroidal 4,5-epoxy-3-ketones.

Cavit Uyanik1, Aslihan Malay, Azra S Ayna, James R Hanson, Peter B Hitchcock.   

Abstract

The stereochemistry of the addition of methylmagnesium bromide to a steroidal 4,5-epoxy-3-ketone has been shown to be determined by the stereochemistry of the epoxide. The epoxidation to the corresponding 3-alkyl-3-hydroxy-4-enes by per-acid was determined by the stereochemistry of the allylic alcohol.

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Year:  2004        PMID: 15631862     DOI: 10.1016/j.steroids.2004.09.002

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


  1 in total

1.  A Peroxygenase from Chaetomium globosum Catalyzes the Selective Oxygenation of Testosterone.

Authors:  Jan Kiebist; Kai-Uwe Schmidtke; Jörg Zimmermann; Harald Kellner; Nico Jehmlich; René Ullrich; Daniel Zänder; Martin Hofrichter; Katrin Scheibner
Journal:  Chembiochem       Date:  2017-03-01       Impact factor: 3.164

  1 in total

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