Enantioselective Michael Addition of Malonates to Chalcone Derivatives Catalyzed by Dipeptide-derived Multifunctional Phosphonium Salts-Reference-Cited by-同舟云学术

Enantioselective Michael Addition of Malonates to Chalcone Derivatives Catalyzed by Dipeptide-derived Multifunctional Phosphonium Salts

Published:2016-10-06 Issue:20 Volume:81 Page:9973-9982
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cao Dongdong¹,Fang Guosheng¹,Zhang Jiaxing¹,Wang Hongyu¹,Zheng Changwu¹,Zhao Gang¹

Affiliation:

1. Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b01752

Reference68 articles.

1. A Catalytic Enantioselective Michael Addition of a Simple Malonate to Prochiral ?,?-Unsaturated Ketoses and Aldehydes

2. Asymmetric Michael Addition of Malonate Anions to Prochiral Acceptors Catalyzed by l-Proline Rubidium Salt

3. A General Organocatalytic Enantioselective Malonate Addition to α,β-Unsaturated Enones

4. Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst

5. Enantioselective Synthesis of Both Enantiomers of Methyl Dihydrojasmonate Using Solid−Liquid Asymmetric Phase-Transfer Catalysis

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