Enantioselective Cyanoethoxycarbonylation of Isatins Promoted by a Lewis Base-Broensted Acid Cooperative Catalyst

Teaming up to make it happen: In the title reaction, the Lewis basic site of the catalyst activated ethyl cyanoformate, and the deep and flexible Broensted acidic cavity stabilized and selectively recognized the key reaction intermediate to promote asymmetric acylation (see scheme).

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Veröffentlicht in:Angewandte Chemie International Edition 2013-08, Vol.52 (32), p.8299-8303
Hauptverfasser: Ogura, Yoshihiro, Akakura, Matsujiro, Sakakura, Akira, Ishihara, Kazuaki
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container_end_page 8303
container_issue 32
container_start_page 8299
container_title Angewandte Chemie International Edition
container_volume 52
creator Ogura, Yoshihiro
Akakura, Matsujiro
Sakakura, Akira
Ishihara, Kazuaki
description Teaming up to make it happen: In the title reaction, the Lewis basic site of the catalyst activated ethyl cyanoformate, and the deep and flexible Broensted acidic cavity stabilized and selectively recognized the key reaction intermediate to promote asymmetric acylation (see scheme).
doi_str_mv 10.1002/anie.201303572
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source Wiley Online Library Journals Frontfile Complete
subjects Activated
Acylation
Asymmetry
Catalysts
Holes
Recognition
title Enantioselective Cyanoethoxycarbonylation of Isatins Promoted by a Lewis Base-Broensted Acid Cooperative Catalyst
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