Abstract
This article presents a comprehensive review of synthetically useful intramolecular annulation reactions of nitrene and nitrenoid intermediates leading to heterocyclic compounds. Thermal, photochemical, and metal mediated reactions of aryl- and vinylazides, azirines, nitroso, and nitro compounds leading to synthetically useful yields of heterocycles are discussed.
Current Organic Chemistry
Title: Synthesis of Heterocycles via Intramolecular Annulation of Nitrene Intermediates
Volume: 4 Issue: 7
Author(s): Bjorn C G. Soderberg
Affiliation:
Abstract: This article presents a comprehensive review of synthetically useful intramolecular annulation reactions of nitrene and nitrenoid intermediates leading to heterocyclic compounds. Thermal, photochemical, and metal mediated reactions of aryl- and vinylazides, azirines, nitroso, and nitro compounds leading to synthetically useful yields of heterocycles are discussed.
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Cite this article as:
G. Soderberg C Bjorn, Synthesis of Heterocycles via Intramolecular Annulation of Nitrene Intermediates, Current Organic Chemistry 2000; 4 (7) . https://dx.doi.org/10.2174/1385272003376067
DOI https://dx.doi.org/10.2174/1385272003376067 |
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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