Copper-Catalyzed Asymmetric Protoboration of β-Amidoacrylonitriles and β-Amidoacrylate Esters: An Efficient Approach to Functionalized Chiral α-Amino Boronate Esters-Reference-Cited by-同舟云学术

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Copper-Catalyzed Asymmetric Protoboration of β-Amidoacrylonitriles and β-Amidoacrylate Esters: An Efficient Approach to Functionalized Chiral α-Amino Boronate Esters

Published:2017-06-21 Issue:13 Volume:19 Page:3676-3679
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Chen Lili¹²,Zou Xiaoliang¹,Zhao Haonan¹,Xu Senmiao¹^ORCID

Affiliation:

1. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Suzhou Research Institute, Lanzhou Institute of Chemical Physics (LICP), Chinese Academy of Sciences, Lanzhou 73000, China

2. University of Chinese Academy of Sciences, Beijing 100049, China

Funder

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Chinese Communist Party Central Committee

Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b01740

Reference71 articles.

1. Synthesis and Pharmacology of Proteasome Inhibitors

2. Synthesis of α-aminoboronic acids

3. Boron chemicals in diagnosis and therapeutics

4. Boron Containing Compounds as Protease Inhibitors

5. Building on bortezomib: second-generation proteasome inhibitors as anti-cancer therapy

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