AZULENOPENTATHIEPIN: PREPARATION AND CONVERSION INTO AZULENES WITH SULFUR GROUPS AT THE 1-AND 2-POSITIONS

被引：7

作者：

Sato, Ohki ^{[1
]}

Sakai, Atsushi ^{[1
]}

Aoki, Masami ^{[1
]}

Kuramochi, Takaaki ^{[1
]}

Nakayama, Juzo ^{[1
]}

机构：

[1] Saitama Univ, Grad Sch Sci & Engn, Dept Chem, Sakura Ku, Saitama 3388570, Japan

来源：

HETEROCYCLES | 2012年 / 86卷 / 02期

关键词：

Azulene; Pentathiepin; Elemental Sulfur; Pyridine; Sulfur Group; PENTATHIEPINS; TETRACYANOAZULENEQUINODIMETHANES; SUBSTITUTION; DERIVATIVES;

D O I：

10.3987/COM-12-S(N)80

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Azulenopentathiepin was prepared by the reaction of azulene with elemental sulfur in boiling pyridine. Bis(thiolate) generated from the pentathiepin reacted with electrophiles such as iodomethane, methyl chloroformate, N,N'-carbonyldiimidazole and N,N'-thiocarbonyldiimidazole to afford the corresponding azulene derivatives. Desulfuration of the pentathiepin and the successive reaction with DMAD or a Pd(0) reagent afforded a 1,4-dithiin compound or Pd complexes.

引用

页码：1253 / 1260

页数：8

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