An efficient sulfenylation of aromatics using highly active quinone mono O,S-acetal bearing a pentafluorophenylthio group

被引：57

作者：

Matsugi, M ^{[1
]}

Murata, K ^{[1
]}

Nambu, H ^{[1
]}

Kita, Y ^{[1
]}

机构：

[1] Osaka Univ, Grad Sch Pharmaceut Sci, Suita, Osaka 5650871, Japan

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 06期

关键词：

D O I：

10.1016/S0040-4039(00)02186-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A facile sulfenylation of various aromatic nuclei was achieved by use of the novel sulfenylation reagent, the quinone mono O,S-acetal bearing a pentafluorophenylthio group. This reagent functions below 0 degreesC in the presence of a catalytic amount of TMSOTf. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：1077 / 1080

页数：4

共 3 条

[1] Facile and efficient sulfenylation method using quinone mono-O,S-acetals under mild conditions
Matsugi, M
Murata, K
Gotanda, K
Nambu, H
Anilkumar, G
Matsumoto, K
Kita, Y
JOURNAL OF ORGANIC CHEMISTRY, 2001, 66 (07): : 2434 - 2441
[2] A novel efficient sulfenylation method using quinone mono-O,S-acetals under mild conditions
Matsugi, M
Gotanda, K
Murata, K
Kita, Y
CHEMICAL COMMUNICATIONS, 1997, (15) : 1387 - 1388
[3] Isolation of the quinone mono O,S-acetal intermediates of the aromatic pummerer-type rearrangement of p-sulfinylphenols with 1-ethoxyvinyl esters
Kita, Y
Takeda, Y
Matsugi, M
Iio, K
Gotanda, K
Murata, K
Akai, S
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1997, 36 (13-14): : 1529 - 1531

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