A mild, nonacidic method for the conversion of carboxylic esters into oxazolines

John H. Dod; Jihua Guan; Charles F. Schwender

doi:10.1080/00397919308013297

A mild, nonacidic method for the conversion of carboxylic esters into oxazolines

John H. Dod, Jihua Guan, Charles F. Schwender

Chemistry

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

9 Scopus citations

Abstract

Conversion of carboxylic esters directly into amide alcohols is facilitated by use of base. Combined with a nonacidic cyclization of the intermediate amide alcohol this method allows formation of oxazolines under nonacidic conditions directly from the carboxylic esters.

Original language	English (US)
Pages (from-to)	1003-1008
Number of pages	6
Journal	Synthetic Communications
Volume	23
Issue number	7
DOIs	https://doi.org/10.1080/00397919308013297
State	Published - Apr 1 1993

All Science Journal Classification (ASJC) codes

Organic Chemistry

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10.1080/00397919308013297

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title = "A mild, nonacidic method for the conversion of carboxylic esters into oxazolines",

abstract = "Conversion of carboxylic esters directly into amide alcohols is facilitated by use of base. Combined with a nonacidic cyclization of the intermediate amide alcohol this method allows formation of oxazolines under nonacidic conditions directly from the carboxylic esters.",

author = "Dod, {John H.} and Jihua Guan and Schwender, {Charles F.}",

year = "1993",

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doi = "10.1080/00397919308013297",

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T1 - A mild, nonacidic method for the conversion of carboxylic esters into oxazolines

AU - Dod, John H.

AU - Guan, Jihua

AU - Schwender, Charles F.

PY - 1993/4/1

Y1 - 1993/4/1

N2 - Conversion of carboxylic esters directly into amide alcohols is facilitated by use of base. Combined with a nonacidic cyclization of the intermediate amide alcohol this method allows formation of oxazolines under nonacidic conditions directly from the carboxylic esters.

AB - Conversion of carboxylic esters directly into amide alcohols is facilitated by use of base. Combined with a nonacidic cyclization of the intermediate amide alcohol this method allows formation of oxazolines under nonacidic conditions directly from the carboxylic esters.

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DO - 10.1080/00397919308013297

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JO - Synthetic Communications

JF - Synthetic Communications

IS - 7

ER -

A mild, nonacidic method for the conversion of carboxylic esters into oxazolines

Abstract

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