4.8 Article

Diversified Cycloisomerization/Diels-Alder Reactions of 1,6-Enynes through Bimetallic Relay Asymmetric Catalysis

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 16, 页码 5327-5331

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201900421

关键词

1,6-enynes; asymmetric catalysis; bimetallic catalysis; cycloisomerization; Diels-Alder reactions

资金

  1. National Natural Science Foundation of China [21890723, 21772127]

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We report the combination of transition-metal-catalyzed diversified cycloisomerization of 1,6-enynes with chiral Lewis acid promoted asymmetric Diets-Alder reaction to realize asymmetric cycloisomerization/Diels-Alder relay reactions of 1,6-enynes with electron-deficient alkenes. A broad spectrum of chiral [5,6]-bicyclic products could be acquired in high yields (up to 99 %) with excellent diastereoselectivy (> 19:1 dr) and enantioselectivity (up to 99 % ee).

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