Aromatic Halogenation Using N-Halosuccinimide and PhSSiMe3 or PhSSPh-Reference-Cited by-同舟云学术

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Aromatic Halogenation Using N-Halosuccinimide and PhSSiMe3 or PhSSPh

Published:2019-04-25 Issue:11 Volume:84 Page:7405-7410
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hirose Yuuka¹,Yamazaki Mirai¹,Nogata Misa¹,Nakamura Akira¹,Maegawa Tomohiro¹^ORCID

Affiliation:

1. School of Pharmaceutical Sciences, Kindai University, Higashi-Osaka, Osaka 577-8502, Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00817

Reference43 articles.

1. Biological Radical Sulfur Insertion Reactions

2. Enzymatic Carbon–Sulfur Bond Formation in Natural Product Biosynthesis

3. 1,3-Dibromo-5,5-Dimethylhydantoin [DBDMH] as an Efficient and Selective Agent for the Oxidation of Thiols to Disulfides in Solution or under Solvent-Free Conditions

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3. Dabco-catalysed selective chlorination of aromatics;Tetrahedron Letters;2024-02

4. Halogenation of aromatic compounds with N-halosuccinimides (NXS) catalysed by d-camphorsulfonic acid-BiCl₃;Organic & Biomolecular Chemistry;2024

5. Aromatic halogenation using carborane catalyst;Chem;2024-01

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