Gold‐Catalyzed [3+2]‐Annulations of α‐Aryl Diazoketones with the Tetrasubstituted Alkenes of Cyclopentadienes: High Stereoselectivity and Enantioselectivity-Reference-Cited by-同舟云学术

Gold‐Catalyzed [3+2]‐Annulations of α‐Aryl Diazoketones with the Tetrasubstituted Alkenes of Cyclopentadienes: High Stereoselectivity and Enantioselectivity

Published:2021-01-15 Issue:9 Volume:60 Page:4479-4484
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Chen Ching‐Nung¹,Cheng Wei‐Min¹,Wang Jian‐Kai¹,Chao Tzu‐Hsuan²,Cheng Mu‐Jeng²^ORCID,Liu Rai‐Shung¹^ORCID

Affiliation:

1. Frontier Research Center for Matter Science and Technology and Department of Chemistry National Tsing-Hua University Hsinchu Taiwan, ROC

2. Department of Chemistry National Cheng Kung University East District Tainan City Taiwan, ROC

Funder

Ministry of Science and Technology, Taiwan

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202012611

Reference62 articles.

1. For reviews for catalytic cyclopropanations see:

2. Stereoselective Cyclopropanation Reactions

3. Recent developments in asymmetric cyclopropanation

4. Gold-catalyzed cyclopropanation reactions using a carbenoid precursor toolbox

5. Recent advances in the synthesis of cyclopropanes

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