Efficient synthetic method for L-tartaramides by aminolysis of reactive 2,3-O-isopropylidene-L-tartaryl chloride

Article abstract of DOI:10.1080/00397919708003365

The reactive 2,3-O-isopropylidene L-tartaryl chloride 4 was firstly synthesized from L-(+)-tartaric acid. Various chiral 2,3-O-isopropylidene-L-tartaramides 5 were prepared by aminolysis of the reactive L-tartaryl chloride 4 with primary and secondary ami

Full text of DOI:10.1080/00397919708003365

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Synthetic Communications: An
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Efficient Synthetic Method for
l-Tartaramides by Aminolysis of
Reactive 2,3-O-Isopropylidene-
L-tartaryl Chloride
a
a
b
Heung-Jin Choi , Mi-Ok Kwak & Hanchul Song
a
Department of Industrial Chemistry, Kyungpook
National University, Taegu, 702-701, Korea
b
Department of Dyeing and Finishing, Kyungpook
National University, Taegu, 702-701, Korea
Published online: 22 Aug 2006.
To cite this article: Heung-Jin Choi , Mi-Ok Kwak & Hanchul Song (1997) Efficient
Synthetic Method for l-Tartaramides by Aminolysis of Reactive 2,3-O-Isopropylidene-
L-tartaryl Chloride, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 27:7, 1273-1280, DOI:
10.1080/00397919708003365
To link to this article: http://dx.doi.org/10.1080/00397919708003365
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