Abstract
This first part of this article focuses on natural products bearing a bicyclo[3.2.0]heptane skeleton. The second part deals with the synthesis of such natural products by focusing on the formation of the bicycloheptane substructure.
Keywords: Bicycloheptane, photochemical [2+2] cycloaddition, Lewis acid catalyzed [2+2] cycloadditon, ntramolecular Diels Alder, Pauson Khand
Current Organic Synthesis
Title: Natural Products Bearing a Bicyclo[3.2.0]Heptane Skeleton
Volume: 3 Issue: 3
Author(s): Michel Miesch
Affiliation:
Keywords: Bicycloheptane, photochemical [2+2] cycloaddition, Lewis acid catalyzed [2+2] cycloadditon, ntramolecular Diels Alder, Pauson Khand
Abstract: This first part of this article focuses on natural products bearing a bicyclo[3.2.0]heptane skeleton. The second part deals with the synthesis of such natural products by focusing on the formation of the bicycloheptane substructure.
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Cite this article as:
Miesch Michel, Natural Products Bearing a Bicyclo[3.2.0]Heptane Skeleton, Current Organic Synthesis 2006; 3 (3) . https://dx.doi.org/10.2174/157017906777934908
DOI https://dx.doi.org/10.2174/157017906777934908 |
Print ISSN 1570-1794 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6271 |
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