Abstract
Different synthetic strategies to 4,4-disubstituted pyridazines and condensed pyridazines with a special reference to the synthetic routes to their spiro analogues are comprehensively outlined in this review.
Keywords: Spirocyclic pyridazines, partially-saturated pyridazines, synthesis, retro- Diels-Alder, 1, 3-dipolar cycloaddition, Aza-Michael addition, nucleophilic reactions.
Graphical Abstract
Current Organic Chemistry
Title:Synthetic Routes to Spirocyclic Pyridazines, Partially-Saturated Pyridazines and Their Condensed Derivatives
Volume: 20 Issue: 14
Author(s): Amr M. Abdelmoniem and Ismail A. Abdelhamid
Affiliation:
Keywords: Spirocyclic pyridazines, partially-saturated pyridazines, synthesis, retro- Diels-Alder, 1, 3-dipolar cycloaddition, Aza-Michael addition, nucleophilic reactions.
Abstract: Different synthetic strategies to 4,4-disubstituted pyridazines and condensed pyridazines with a special reference to the synthetic routes to their spiro analogues are comprehensively outlined in this review.
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Cite this article as:
M. Abdelmoniem Amr and A. Abdelhamid Ismail, Synthetic Routes to Spirocyclic Pyridazines, Partially-Saturated Pyridazines and Their Condensed Derivatives, Current Organic Chemistry 2016; 20 (14) . https://dx.doi.org/10.2174/1385272820666160216224951
DOI https://dx.doi.org/10.2174/1385272820666160216224951 |
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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