Catalytic Enantioselective Double Carbopalladation/C−H Functionalization with Statistical Amplification of Product Enantiopurity: A Convertible Linker Approach-Reference-Cited by-同舟云学术

Catalytic Enantioselective Double Carbopalladation/C−H Functionalization with Statistical Amplification of Product Enantiopurity: A Convertible Linker Approach

Published:2017-10-04 Issue:45 Volume:129 Page:14380-14384
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Tong Shuo¹,Limouni Aurore¹,Wang Qian¹,Wang Mei-Xiang²,Zhu Jieping¹^ORCID

Affiliation:

1. Laboratory of Synthesis and Natural Products; Institute of Chemical Sciences and Engineering; Ecole Polytechnique Fédérale de Lausanne, EPFL-SB-ISIC-LSPN, BCH 5304; 1015 Lausanne Switzerland

2. Laboratory of Bioorganic Phosphorous Chemistry and Chemical Biology, Ministry of Education; Department of Chemistry; Tsinghua University; Beijing 100084 China

Publisher

Wiley

Subject

General Medicine

Reference64 articles.

1. A convenient method for upgrading the enantiomeric purities of (+)-longifolene and (+)-3-carene to materials approaching 100% ee

2. Zirconium-Catalyzed Asymmetric Carboalumination of Alkenes: ZACA–Lipase-Catalyzed Acetylation Synergy

3. Nouvelle methode pour porter au maximum la purete optique d'un produit partiellement dedouble sans l'aide d'aucune substance chirale

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