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

Article abstract of DOI:10.1080/00397919308013297

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 car

Full text of DOI:10.1080/00397919308013297

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Synthetic Communications: An
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A Mild, Nonacidic Method for
the Conversion of Carboxylic
Esters into Oxazolines
J. H. Dodd a , J. Guan a & C. F. Schwender a
a The R. W. Johnson Pharmaceutical Research
Institute, 1000 Route 202 Raritan, New Jersey, 08869
Version of record first published: 23 Sep 2006.
To cite this article: J. H. Dodd , J. Guan & C. F. Schwender (1993): A Mild,
Nonacidic Method for the Conversion of Carboxylic Esters into Oxazolines, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 23:7, 1003-1008
To link to this article: http://dx.doi.org/10.1080/00397919308013297
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