One-pot synthesis of 2,4,5-trisubstituted oxazoles from N-acyl amino acids by a combination of cyclodehydration with N,N′-diisopropylcarbodiimide and Wittig olefination-Reference-Cited by-同舟云学术

One-pot synthesis of 2,4,5-trisubstituted oxazoles from N-acyl amino acids by a combination of cyclodehydration with N,N′-diisopropylcarbodiimide and Wittig olefination

Published:2012-01 Issue:4 Volume:68 Page:977-981
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Huang Wenhua,Dong Guangping,Mijiti Zumureti

Funder

Tianjin University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. Recent advances in the total syntheses of oxazole-containing natural products

2. Thiazole and Oxazole Alkaloids: Isolation and Synthesis

3. An efficient synthesis of ethyl 5-oxazoleacetates

4. Electronically Mediated Selectivity in Ring Opening of 1-Azirines. The 3-X Mode: Convenient Route to 3-Oxazolines

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3. Single-Step Synthesis of Iodinated Oxazoles from N-Propargyl Amides Mediated by I2/Iodosylbenzene/Trimethylsilyl Trifluoromethanesulfonate Systems;The Journal of Organic Chemistry;2017-08-25

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5. ChemInform Abstract: One-Pot Synthesis of 2,4,5-Trisubstituted Oxazoles from N-Acyl Amino Acids by a Combination of Cyclodehydration with N,N′-Diisopropylcarbodiimide and Wittig Olefination.;ChemInform;2012-06-11