Tetrahedron letters2022,Vol.884.DOI:10.1016/j.tetlet.2021.153554

A new approach for the synthesis of N-beta-enaminocarbonyl 2-oxazolidinones through ring transformation reactions of uracil

Kitamura, Yoshiaki Ohshima, Yuto Nagaya, Yuki
Tetrahedron letters2022,Vol.884.DOI:10.1016/j.tetlet.2021.153554

A new approach for the synthesis of N-beta-enaminocarbonyl 2-oxazolidinones through ring transformation reactions of uracil

Kitamura, Yoshiaki 1Ohshima, Yuto 1Nagaya, Yuki1
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作者信息

  • 1. Gifu Univ
  • 折叠

Abstract

The reaction of N-1-sulfonyluracil derivatives bearing a 2-hydroxyethyl moiety at the 3-position with NaH under anhydrous conditions at room temperature affords the corresponding 2-oxazolidinone bearing the beta-enaminocarbonyl moiety. These products are useful diversifiable precursors toward various beta-amino acids and N-heterocyclic compounds. (C) 2021 Elsevier Ltd. All rights reserved.

Key words

beta-Enaminocarbonyl compounds/2-Oxazolidinone/Ring transformation/Uracil/STEREOSELECTIVE-SYNTHESIS/ACID-DERIVATIVES/AMINO/COMPLEXES/CATALYSTS/ENAMINES

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出版年

2022
Tetrahedron letters

Tetrahedron letters

CCR
ISSN:0040-4039
被引量1
参考文献量26
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