A Tunable Route to Prepare α,β-Unsaturated Esters and α,β-Unsaturated-γ-Keto Esters through Copper-Catalyzed Coupling of Alkenyl Boronic Acids with Phosphorus Ylides-Reference-Cited by-同舟云学术

A Tunable Route to Prepare α,β-Unsaturated Esters and α,β-Unsaturated-γ-Keto Esters through Copper-Catalyzed Coupling of Alkenyl Boronic Acids with Phosphorus Ylides

Published:2018-02-28 Issue:7 Volume:360 Page:1510-1516
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Bi Hong-Yan¹,Liu Feng-Ping¹,Liang Cui¹,Su Gui-Fa¹,Mo Dong-Liang¹

Affiliation:

1. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources; Ministry of Science and Technology of China; School of Chemistry and Pharmaceutical Sciences; Guangxi Normal University; 15 Yu Cai Road Guilin 541004 People's Republic of China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangxi

Ministry of Science and Technology of China

Publisher

Wiley

Subject

General Chemistry

Reference86 articles.

1. Acylvinyl and Vinylogous Synthons

2. Organocatalytic Michael Addition of Aldehydes to γ-Keto-α,β-unsaturated Esters. An Efficient Entry to Versatile Chiral Building Blocks

3. Catalytic Asymmetric Chloroamination Reaction of α,β-Unsaturated γ-Keto Esters and Chalcones

4. Synthesis of pyrrolidine-3-carboxylic acid derivatives via asymmetric Michael addition reactions of carboxylate-substituted enones

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