Abstract
Certain cycloalkane-anellated heterocycles undergo rearrangement under basic or acidic conditions via ring-contraction, ringexpansion or ring-opening pathways to afford new or unusual compounds. The reactivities and properties of cycloalkane-fused heterocycles differ significantly from those of heteroaromatic ring systems. Possible mechanisms are also discussed.
Current Organic Chemistry
Title: Acid- and Base-Promoted Rearrangements of Cycloalkane-Fused Heterocycles
Volume: 14 Issue: 8
Author(s): Ferenc Csende, Ferenc Miklos and Andrea Porkolab
Affiliation:
Abstract: Certain cycloalkane-anellated heterocycles undergo rearrangement under basic or acidic conditions via ring-contraction, ringexpansion or ring-opening pathways to afford new or unusual compounds. The reactivities and properties of cycloalkane-fused heterocycles differ significantly from those of heteroaromatic ring systems. Possible mechanisms are also discussed.
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Cite this article as:
Csende Ferenc, Miklos Ferenc and Porkolab Andrea, Acid- and Base-Promoted Rearrangements of Cycloalkane-Fused Heterocycles, Current Organic Chemistry 2010; 14 (8) . https://dx.doi.org/10.2174/138527210791111867
DOI https://dx.doi.org/10.2174/138527210791111867 |
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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