Abstract
The oxidation of steroidal olefins allows the incorporation of functional groups into their skeleton and accounts for the obtention of valuable intermediates in the synthesis of pharmaceuticals, agrochemical and other fine chemicals. The catalytic epoxidation and syn-dihydroxylation reactions of steroidal alkenes are reviewed.
Current Organic Chemistry
Title: Catalytic Epoxidation and syn-Dihydroxylation Reactions in Steroid Chemistry
Volume: 12 Issue: 6
Author(s): Jorge A.R. Salvador, Samuel M. Silvestre and Vania M. Moreira
Affiliation:
Abstract: The oxidation of steroidal olefins allows the incorporation of functional groups into their skeleton and accounts for the obtention of valuable intermediates in the synthesis of pharmaceuticals, agrochemical and other fine chemicals. The catalytic epoxidation and syn-dihydroxylation reactions of steroidal alkenes are reviewed.
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Cite this article as:
Salvador A.R. Jorge, Silvestre M. Samuel and Moreira M. Vania, Catalytic Epoxidation and syn-Dihydroxylation Reactions in Steroid Chemistry, Current Organic Chemistry 2008; 12 (6) . https://dx.doi.org/10.2174/138527208784083897
DOI https://dx.doi.org/10.2174/138527208784083897 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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