Regio- and Enantioselective Iridium-Catalyzed Allylic Alkylation with In Situ Activated P,C-Chelate Complexes
Come together: Successful cooperation of iridium and copper yielded a new catalyst system for allylic alkylation. Branched alkylation products can be obtained rapidly and with high enantioselectivity from simple linear precursors (see scheme; cod=cyclooctadiene).
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Published in | Angewandte Chemie International Edition Vol. 43; no. 35; pp. 4595 - 4597 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
06.09.2004
WILEY‐VCH Verlag Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | Come together: Successful cooperation of iridium and copper yielded a new catalyst system for allylic alkylation. Branched alkylation products can be obtained rapidly and with high enantioselectivity from simple linear precursors (see scheme; cod=cyclooctadiene). |
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Bibliography: | ark:/67375/WNG-9B1GBNQS-0 This work was supported by the Deutsche Forschungsgemeinschaft (SFB 623) and by the Fonds der Chemischen Industrie. We thank Markus Krauter for competent experimental assistance, Dr. F. Rominger for the X-ray crystal structure, and Degussa AG for iridium salts. ArticleID:ANIE200460016 istex:4632E838B1D5331FB5D34A36B217DFA258F40EF0 This work was supported by the Deutsche Forschungsgemeinschaft (SFB 623) and by the Fonds der Chemischen Industrie. We thank Markus Krauter for competent experimental assistance, Dr. F. Rominger for the X‐ray crystal structure, and Degussa AG for iridium salts. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.200460016 |