Access to Benzocyclic Boronates via Light-Promoted Intramolecular Arylborylation of Alkenes-Reference-Cited by-同舟云学术

Access to Benzocyclic Boronates via Light-Promoted Intramolecular Arylborylation of Alkenes

Published:2023-04-11 Issue:9 Volume:88 Page:6237-6246
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ke Sen¹,Liao Huanqing¹,Qin Hao¹,Wang Yan¹,Li Yi¹^ORCID

Affiliation:

1. Key Laboratory of Molecule Synthesis and Function Discovery (Fujian Province University), College of Chemistry, Fuzhou University, Fuzhou 350108, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c00395

Reference70 articles.

1. 1,3,2-Benzodioxaborole, a convenient monofunctional hydroborating agent. Simple new synthesis of alkaneboronic esters and acids from olefins via hydroboration

2. Lithiation–Borylation Methodology and Its Application in Synthesis

3. Synthesis and Applications of Boronic Acid-Containing Polymers: From Materials to Medicine

4. Stereospecific functionalizations and transformations of secondary and tertiary boronic esters

5. Tetracoordinate Boron Intermediates Enable Unconventional Transformations

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