Enantioselective Epoxidation of β,γ-Unsaturated Carboxylic Acids by a Cooperative Binuclear Titanium Complex
Enantioselective epoxidation of β,γ-unsaturated carboxylic acids with a cooperative binuclear titanium complex has been developed to provide single diastereomer γ-lactones in high yields and enantioselectivities via intramolecular cyclization. For the success of the reaction, the proper distance bet...
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Published in: | ACS catalysis Vol. 9; no. 4; pp. 3384 - 3388 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
American Chemical Society
05-04-2019
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Subjects: | |
Online Access: | Get full text |
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Summary: | Enantioselective epoxidation of β,γ-unsaturated carboxylic acids with a cooperative binuclear titanium complex has been developed to provide single diastereomer γ-lactones in high yields and enantioselectivities via intramolecular cyclization. For the success of the reaction, the proper distance between the carboxylic acid and alkene is quite important, offering the regioselective epoxidation of unsaturated carboxylic acids bearing two similar alkenes. |
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ISSN: | 2155-5435 2155-5435 |
DOI: | 10.1021/acscatal.9b00840 |