Diastereoselective Intramolecular Hydride Transfer Triggered by Electrophilic Halogenation of Aryl Alkenes-Reference-Cited by-同舟云学术

Diastereoselective Intramolecular Hydride Transfer Triggered by Electrophilic Halogenation of Aryl Alkenes

Published:2019-11-01 Issue:22 Volume:21 Page:9179-9182
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Bin¹,Gandamana Dhika Aditya¹,León Rayo David Fabian²,Gagosz Fabien²^ORCID,Chiba Shunsuke¹^ORCID

Affiliation:

1. Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore

2. Department of Chemistry and Biomolecular Sciences, University of Ottawa, K1N 6N5, Ottawa, Canada

Funder

Ministry of Education - Singapore

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b03548

Reference54 articles.

1. Catalytic, Stereoselective Dihalogenation of Alkenes: Challenges and Opportunities

2. Recent advances in stereoselective bromofunctionalization of alkenes using N-bromoamide reagents

3. Iodine electrophiles in stereoselective reactions: recent developments and synthetic applications

4. Halo- and selenolactonisation: the two major strategies for cyclofunctionalisation

5. Diastereoselective Intramolecular Hydride Transfer under Brønsted Acid Catalysis

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