Tin(II) chloride-mediated synthesis of 2-substituted benzoxazoles

Chan Sik Cho; Dong Tak Kim; Jiao Qiang Zhang; Son Lam Ho; Tae Jeong Kim; Sang Chul Shim

doi:10.1002/jhet.5570390229

Tin(II) chloride-mediated synthesis of 2-substituted benzoxazoles

Chan Sik Cho, Dong Tak Kim, Jiao Qiang Zhang, Son Lam Ho, Tae Jeong Kim, Sang Chul Shim

Department of Applied Chemistry

Kyungpook National University

Research output: Contribution to journal › Article › peer-review

29 Scopus citations

Abstract

2-Aminophenols react with an array of carboxylic acids in dioxane at 180° in the presence of tin(II) chloride to afford the corresponding 2-substituted benzoxazoles in good yields. The reaction is applicable to a wide range of alkyl, alkenyl, aryl carboxylic acids.

Original language	English
Pages (from-to)	421-423
Number of pages	3
Journal	Journal of Heterocyclic Chemistry
Volume	39
Issue number	2
DOIs	https://doi.org/10.1002/jhet.5570390229
State	Published - 2002

Access to Document

10.1002/jhet.5570390229

Cite this

@article{94d940dd7b0a40169d4590191e556b4a,

title = "Tin(II) chloride-mediated synthesis of 2-substituted benzoxazoles",

abstract = "2-Aminophenols react with an array of carboxylic acids in dioxane at 180° in the presence of tin(II) chloride to afford the corresponding 2-substituted benzoxazoles in good yields. The reaction is applicable to a wide range of alkyl, alkenyl, aryl carboxylic acids.",

author = "Cho, \{Chan Sik\} and Kim, \{Dong Tak\} and Zhang, \{Jiao Qiang\} and Ho, \{Son Lam\} and Kim, \{Tae Jeong\} and Shim, \{Sang Chul\}",

year = "2002",

doi = "10.1002/jhet.5570390229",

language = "English",

volume = "39",

pages = "421--423",

journal = "Journal of Heterocyclic Chemistry",

issn = "0022-152X",

publisher = "John Wiley and Sons Inc.",

number = "2",

}

TY - JOUR

T1 - Tin(II) chloride-mediated synthesis of 2-substituted benzoxazoles

AU - Cho, Chan Sik

AU - Kim, Dong Tak

AU - Zhang, Jiao Qiang

AU - Ho, Son Lam

AU - Kim, Tae Jeong

AU - Shim, Sang Chul

PY - 2002

Y1 - 2002

N2 - 2-Aminophenols react with an array of carboxylic acids in dioxane at 180° in the presence of tin(II) chloride to afford the corresponding 2-substituted benzoxazoles in good yields. The reaction is applicable to a wide range of alkyl, alkenyl, aryl carboxylic acids.

AB - 2-Aminophenols react with an array of carboxylic acids in dioxane at 180° in the presence of tin(II) chloride to afford the corresponding 2-substituted benzoxazoles in good yields. The reaction is applicable to a wide range of alkyl, alkenyl, aryl carboxylic acids.

UR - https://www.scopus.com/pages/publications/0036098226

U2 - 10.1002/jhet.5570390229

DO - 10.1002/jhet.5570390229

M3 - Article

AN - SCOPUS:0036098226

SN - 0022-152X

VL - 39

SP - 421

EP - 423

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 2

ER -

Tin(II) chloride-mediated synthesis of 2-substituted benzoxazoles

Abstract

Access to Document

Other files and links

Fingerprint

Cite this