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Synthesis and structural elucidation of a dehydrochloromethyltestosterone metabolite†
Nicolas Kratena,Sarah M. Pilz,Matthias Weil,Günter Gmeiner,Valentin S. Enev,Peter Gärtner
Organic & Biomolecular Chemistry Pub Date : 03/06/2018 00:00:00 , DOI:10.1039/C8OB00122G
Abstract

The human urinary long-term metabolite “M3” (4-chloro-17β-hydroxymethyl-17α-methyl-18-norandrost-13-en-3-ol) of the common doping agent DHCMT has thus far been detected via GC/MS-MS, creating ambiguities concerning its absolute configuration. Its structure was elucidated via the synthesis of all eight possible stereoisomers with 17β-hydroxymethyl configuration. The highlights of the synthesis consist of a novel first generation approach to 4β-chloro-5β compounds as well as a divergent route which allows easy access to the remaining A-ring chlorohydrins.

Graphical abstract: Synthesis and structural elucidation of a dehydrochloromethyltestosterone metabolite
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