Cu-catalyzed regioselective borylcyanation of 1,3-dienes-Reference-Cited by-同舟云学术

Cu-catalyzed regioselective borylcyanation of 1,3-dienes

Published:2018 Issue:91 Volume:54 Page:12832-12835
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Wen Lu¹²³⁴⁵,Zhang Haiyan¹²³⁴⁵,Wang Jiping¹²³⁴⁵,Meng Fanke¹²³⁴⁵^ORCID

Affiliation:

1. State Key Laboratary of Organometallic Chemistry

2. Center for Excellence in Molecular Synthesis

3. Shanghai Institute of Organic Chemistry

4. University of Chinese Academy of Sciences

5. Chinese Academy of Sciences

Abstract

Catalytic regioselective generation of an allyl–Cu complex through Cu–B(pin) (pin = pinacolato) addition to 1,3-dienes followed by reaction with an electrophilic cyanation reagent to afford multifunctional organoboron compounds is presented.

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC07032F

Reference62 articles.

1. Asymmetric Multicomponent Reactions (AMCRs): The New Frontier

2. Multicomponent Reaction Design in the Quest for Molecular Complexity and Diversity

3. Mechanisms of Nucleophilic Organocopper(I) Reactions

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5. Copper-catalyzed oxidative carbon–heteroatom bond formation: a recent update

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