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Rh-Catalyzed Enantioselective [2 + 2] Cycloaddition of Alkynyl Esters and Norbornene Derivatives
The enantioselective [2 + 2] cycloaddition of alkynes possessing an ester functionality and norbornene derivatives proceeded efficiently using a chiral rhodium catalyst. The chiral tri- and tetracyclic cyclobutenes were obtained in moderate to high ee.
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Published in: | Organic letters 2006-03, Vol.8 (7), p.1343-1345 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The enantioselective [2 + 2] cycloaddition of alkynes possessing an ester functionality and norbornene derivatives proceeded efficiently using a chiral rhodium catalyst. The chiral tri- and tetracyclic cyclobutenes were obtained in moderate to high ee. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/ol060055r |