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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 45, 2015 - Issue 1
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Original Articles

Stereoselective Synthesis of cis- and trans-3,4,5-Trisubstituted-1,3-oxazolidin-2-one Derivatives from 1,2-Amino Alcohol Monoesters and Aziridine-2-carboxylates

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Pages 111-118 | Received 21 May 2014, Published online: 20 Oct 2014
 

Abstract

New cis-N-alkyl-1,3-oxazolidin-2-ones were prepared in moderate to good yields via phosgenation of erythro-1,2-aminoalcohol monoesters, accompanied by formation of aziridine by-products. On the other hand, their regioisomers trans-N-alkyl-1,3-oxazolidin-2-ones were prepared regio- and stereoselectively in good yields by ring expansion of trans-N-alkyl aziridine-2-carboxylates.

GRAPHICAL ABSTRACT

ACKNOWLEDGMENT

We thank N. Gabsi for interesting and valuable English discussions.

Notes

a Yields refer to isolated chromatographically pure compounds.

a Yields refer to isolated chromatographically pure compounds.

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