Diversity in Synthesis of N-Heterocycles from Simple Propargylic Alcohols

被引:12
作者
Gayon, Eric [1 ]
Gerard, Helene [2 ]
Vrancken, Emmanuel [1 ]
Campagne, Jean-Marc [1 ]
机构
[1] Inst Charles Gerhardt, CNRS UM2 UM1 ENSCM UMR 5253, F-34296 Montpellier 5, France
[2] Univ Paris 06, CNRS Case 137, Chim Theor Lab, UMR 7616, F-75262 Paris 05, France
关键词
iron; palladium; heterocycles; isomerization; ring closure; catalysis; ONE-POT SYNTHESIS; HIGHLY SUBSTITUTED ISOXAZOLES; ELECTROPHILIC CYCLIZATION; NUCLEOPHILIC-SUBSTITUTION; O-ALKYNYLPHENOLS; TANDEM REACTION; REARRANGEMENT; DERIVATIVES; 4-ISOXAZOLINES; ACYLAZIRIDINES;
D O I
10.1055/s-0034-1378804
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In this account, we summarize our recent work on the preparation of various N-heterocycles, starting from propargylic alcohols. Our aim was to develop versatile and selective one-pot procedures that would permit the synthesis of large collections of heterocycles, such as di- or tri-substituted isoxazolines and isoxazoles, cis-aziridines, and pyrimidines, by fine changes in the reaction conditions. When needed, mechanistic studies have been performed by combining experimental work with density functional theory calculations. 1 Introduction 2 Synthesis of Disubstituted Isoxazolines 3 Synthesis of Disubstituted Isoxazoles 4 Synthesis of cis-Acylaziridines 5 Trisubstituted Isoxazolines and Isoxazoles 6 -Enaminones and Pyrimidines 7 Conclusion
引用
收藏
页码:2336 / 2350
页数:15
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