Facile and Efficient Sulfenylation Method Using Quinone Mono-O,S-Acetals under Mild Conditions-Reference-Cited by-同舟云学术

Facile and Efficient Sulfenylation Method Using Quinone Mono-O,S-Acetals under Mild Conditions

Published:2001-03-15 Issue:7 Volume:66 Page:2434-2441
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Matsugi Masato¹,Murata Kenji¹,Gotanda Kentoku¹,Nambu Hisanori¹,Anilkumar Gopinathan¹,Matsumoto Keita¹,Kita Yasuyuki¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Osaka University, 1−6 Yamada-oka, Suita, Osaka 565-0871, Japan, and Research Center, Taisho Pharmaceutical Co., Ltd., 1-403 Yoshino-cho, Omiya, Saitama 330-8530, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001710q

Reference17 articles.

1. .alpha.-Sulfenylated carbonyl compounds in organic synthesis

2. Novel ipso-Substitution of p-Sulfinylphenols through the Pummerer-Type Reaction: A Selective and Efficient Synthesis of p-Quinones and Protected p-Dihydroquinones

3. Total Synthesis of the Antitumor Antibiotic (±)-Fredericamycin A by a Linear Approach

4. Ambident Effect of a p-Sulfinyl Group for the Introduction of Two Carbon Substituents to Phenol Rings: A Convergent Synthesis of Diverse Benzofuran Neolignans

Cited by 132 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Regioselective Thiolation of Indole to Construct 3-Arylthioindoles;Current Organic Chemistry;2024-08-19

2. t-BuOLi promoted regioselective N-thiolation of indoles with N-arylthio phthalimide;Organic & Biomolecular Chemistry;2024

3. Recent advances in selective mono-/dichalcogenation and exclusive dichalcogenation of C(sp²)–H and C(sp³)–H bonds;Organic & Biomolecular Chemistry;2024

4. N-Heterocyclic Carbene-Catalyzed Synthesis of Pentafluorophenyl Sulfides;Chinese Journal of Organic Chemistry;2024

5. Silver‐Catalyzed para‐Selective Sulfenyl Group Transfer Reactions of N‐Sulfenylanilides;Chemistry – A European Journal;2023-08-21