Chiral bifunctional sulfide-catalyzed asymmetric bromoaminocyclizations-Reference-Cited by-同舟云学术

Chiral bifunctional sulfide-catalyzed asymmetric bromoaminocyclizations

Published:2020 Issue:17 Volume:18 Page:3367-3373
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Nakamura Takumi¹²³⁴⁵,Okuno Ken¹²³⁴⁵,Kaneko Kazuma⁶⁷⁸⁹⁵,Yamanaka Masahiro⁶⁷⁸⁹⁵^ORCID,Shirakawa Seiji¹²³⁴⁵^ORCID

Affiliation:

1. Department of Environmental Science

2. Graduate School of Fisheries and Environmental Sciences

3. Nagasaki University

4. Nagasaki 852-8521

5. Japan

6. Department of Chemistry and Research Center for Smart Molecules

7. Faculty of Science

8. Rikkyo University

9. Tokyo 171-8501

Abstract

A chiral bifunctional sulfide catalyst bearing a urea moiety promotes the enantioselective bromoaminocyclization of 2-allylanilines to produce optically active 2-substituted indolines.

Funder

Japan Society for the Promotion of Science

Tokuyama Science Foundation

Takahashi Industrial and Economic Research Foundation

Shorai Foundation for Science and Technology

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB00459F

Reference52 articles.

1. Enantioselective Halocyclization Reactions for the Synthesis of Chiral Cyclic Compounds

2. Current Methods for Asymmetric Halogenation of Olefins

3. Catalytic, Asymmetric Halofunctionalization of Alkenes-A Critical Perspective

4. New Catalytic Approaches towards the Enantioselective Halogenation of Alkenes

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