Highly Enantioselective Insertion of Carbenoids into O−H Bonds of Phenols: An Efficient Approach to Chiral α-Aryloxycarboxylic Esters-Reference-Cited by-同舟云学术

Highly Enantioselective Insertion of Carbenoids into O−H Bonds of Phenols: An Efficient Approach to Chiral α-Aryloxycarboxylic Esters

Published:2007-09-29 Issue:42 Volume:129 Page:12616-12617
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Chen Chao¹,Zhu Shou-Fei¹,Liu Bin¹,Wang Li-Xin¹,Zhou Qi-Lin¹

Affiliation:

1. State Key Laboratory and Institute of Elemento-organic Chemistry, Nankai University, Tianjin 300071, China, and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja074729k

Reference10 articles.

1. Catalytic Enantioselective C−H Activation by Means of Metal−Carbenoid-Induced C−H Insertion

2. Asymmetric rhodium carbenoid insertion into the SiH bond

3. Synthesis of oxygen-containing heterocyclic compounds based on the intramolecular O–H insertion and Wolff rearrangement of α-diazocarbonyl compounds

4. Catalytic Enantioselective O−H Insertion Reactions

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