Internal B–O Bond-Facilitated Photoisomerization of Boranes: Ring Expansion Versus Oxyborane Elimination/Intramolecular Diels

Internal B–O Bond-Facilitated Photoisomerization of Boranes: Ring Expansion Versus Oxyborane Elimination/Intramolecular Diels–Alder Addition

Published:2019-06-20 Issue:13 Volume:21 Page:5285-5289
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hu Guo-Fei¹,Li Hai-Jun²,Zeng Chao¹,Wang Xiang²,Wang Nan¹^ORCID,Peng Tai¹,Wang Suning¹²^ORCID

Affiliation:

1. Laboratory of Cluster Science, Ministry of Education of China, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, China

2. Department of Chemistry, Queen’s University, Kingston, Ontario K7L 3N6, Canada

Funder

Natural Sciences and Engineering Research Council of Canada

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b01892

Reference34 articles.

1. Boronic Acids

2. New Directions for Frustrated Lewis Pair Chemistry

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4. Metal-free catalytic C-H bond activation and borylation of heteroarenes

5. Frustrated Lewis Pair Chemistry: Development and Perspectives

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