Enantioselective 1,2-Difunctionalization of 1,3-Butadiene by Sequential Alkylation and Carbonyl Allylation-Reference-Cited by-同舟云学术

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Enantioselective 1,2-Difunctionalization of 1,3-Butadiene by Sequential Alkylation and Carbonyl Allylation

Published:2018-02-14 Issue:8 Volume:140 Page:2735-2738
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Xiong Yang¹,Zhang Guozhu¹^ORCID

Affiliation:

1. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Center for Excellence in Molecular Synthesis, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, People’s Republic of China

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

Central Committee of the Communist Party of China

State Key Laboratory of Organometallic Chemistry

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.7b12760

Reference75 articles.

1. The industrial production and use of 1,3-butadiene.

2. Butadiene production process overview

3. Palladium-catalyzed arylation of conjugated dienes

4. Stereo- and regioselective palladium-catalyzed 1,4-acetoxychlorination of 1,3-dienes. 1-Acetoxy-4-chloro-2-alkenes as versatile synthons in organic transformations

5. Allylsilanes as Carbon Nucleophiles in Intramolecular Pd(II)-Catalyzed 1,4-Addition to Conjugated Dienes

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