Isolation of 3H-indole-3,3 bis-sulfides as intermediates in the second sulfenylation of indole

被引：16

作者：

Hamel, P

机构：

[1] Merck Frosst Ctr. Therapeut. Res., P.O. Box 1005, Pointe-Claire - Dorval

来源：

TETRAHEDRON LETTERS | 1997年 / 38卷 / 49期

关键词：

D O I：

10.1016/S0040-4039(97)10296-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

3H-Indole-3,3 bis sulfides have been isolated as probable intermediates in the second sulfenylation of indole with sulfenyl halides. (C) 1997 Published by Elsevier Science Ltd.

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页码：8473 / 8474

页数：2

相关论文

共 3 条

[1] ALKYLTHIATION AND ARYLTHIATION OF URACIL AND INDOLE [J].

ANZAI, K .

JOURNAL OF HETEROCYCLIC CHEMISTRY, 1979, 16 (03) :567-569

[2] Regioselective synthesis of mixed indole 2,3-bis(sulfides). A study of the mechanism of the second sulfenylation of indole [J].

Hamel, P ;

Preville, P .

JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (05) :1573-1577

[3] CONVERSION OF INDOLE INTO 3-S-(CYSTEINYL)INDOLES AND 2-S-(CYSTEINYL)TRYPTOPHANS - AN APPROACH TO TRYPTATHIONINES [J].

PLATE, R ;

NIVARD, RJF ;

OTTENHEIJM, HCJ .

TETRAHEDRON, 1986, 42 (16) :4503-4509