Anti-Markovnikov Hydroheteroarylation of Unactivated Alkenes with Indoles, Pyrroles, Benzofurans, and Furans Catalyzed by a Nickel–N-Heterocyclic Carbene System-Reference-Cited by-同舟云学术

Anti-Markovnikov Hydroheteroarylation of Unactivated Alkenes with Indoles, Pyrroles, Benzofurans, and Furans Catalyzed by a Nickel–N-Heterocyclic Carbene System

Published:2015-09-16 Issue:38 Volume:137 Page:12215-12218
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Schramm York¹²,Takeuchi Makoto³,Semba Kazuhiko³,Nakao Yoshiaki³⁴,Hartwig John F.¹²

Affiliation:

1. Division of Chemical Sciences, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States

2. Department of Chemistry, University of California, Berkeley, California 94720, United States

3. Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan

4. ACT-C, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan

Funder

Schweizerische Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Ministry of Education, Culture, Sports, Science, and Technology

Office of Science

Japan Science and Technology Agency

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.5b08039

Reference22 articles.

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2. Discovery of Ecopladib, an Indole Inhibitor of Cytosolic Phospholipase Α2α

3. Catalytic Functionalization of Indoles in a New Dimension

4. A review of new developments in the Friedel–Crafts alkylation – From green chemistry to asymmetric catalysis

5. Ir(I)-Catalyzed C–H Bond Alkylation of C2-Position of Indole with Alkenes: Selective Synthesis of Linear or Branched 2-Alkylindoles

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