Abstract
The versatility and potential of reductive cyclisation as a route to 6-membered N-heterocyclic structures of diverse complexity is demonstrated through selected examples.
Keywords: heterocycles, reduction, transformation, quinolines, rh-catalysed hydrogenation, pyridazines
Current Organic Chemistry
Title: Reductive Cyclisation in the Synthesis of 6-Membered N-Heterocycles
Volume: 8 Issue: 16
Author(s): Petros G. Tsoungas and Andreas I. Diplas
Affiliation:
Keywords: heterocycles, reduction, transformation, quinolines, rh-catalysed hydrogenation, pyridazines
Abstract: The versatility and potential of reductive cyclisation as a route to 6-membered N-heterocyclic structures of diverse complexity is demonstrated through selected examples.
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Cite this article as:
Tsoungas G. Petros and Diplas I. Andreas, Reductive Cyclisation in the Synthesis of 6-Membered N-Heterocycles, Current Organic Chemistry 2004; 8 (16) . https://dx.doi.org/10.2174/1385272043369737
DOI https://dx.doi.org/10.2174/1385272043369737 |
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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