One-pot tandem approach for the synthesis of benzimidazoles and benzothiazoles from alcohols

被引：100

作者：

Raghavendra, Goravanahalli M. ^{[1
]}

Ramesha, Ajjahalli B. ^{[1
]}

Revanna, Cigalli N. ^{[1
]}

Nandeesh, Kebbahalli N. ^{[1
]}

Mantelingu, Kempegowda ^{[1
]}

Rangappa, Kanchugarakoppal S. ^{[1
]}

机构：

[1] Univ Mysore, Dept Studies Chem, Mysore 570006, Karnataka, India

来源：

TETRAHEDRON LETTERS | 2011年 / 52卷 / 43期

关键词：

(R) T3P; Benzimidazole; Benzothiazole; o-Diaminoarenes; o-Aminothiophenols; 2-SUBSTITUTED BENZIMIDAZOLES; EFFICIENT METHOD; HETEROCYCLES; DERIVATIVES; INHIBITORS; AGENTS; DNA;

D O I：

10.1016/j.tetlet.2011.08.037

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Propylphosphonic anhydride ((R) T3P) has been demonstrated to be an efficient and mild reagent for the one-pot synthesis of benzimidazoles and benzothiazoles from variety of alcohols. Mild conditions, short reaction time, broad functional group tolerance, low epimerization, easy and quick isolation of the products, excellent chemo selectivity, and excellent yields are main advantages of this procedure. Thus, the present method is utilizing alcohols instead of aldehydes. (C) 2011 Elsevier Ltd. All rights reserved.

引用

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页码：5571 / 5574

页数：4

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