Utilisation of Enols of Mono- and Dicarbonyls Compounds in 1,3-Dipolar Cycloaddition Reactions-Reference-Cited by-同舟云学术

Utilisation of Enols of Mono- and Dicarbonyls Compounds in 1,3-Dipolar Cycloaddition Reactions

Published:2003-05 Issue:5 Volume:2003 Page:254-255
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Kurkowska Joanna¹,Zadrożna Irmina¹

Affiliation:

1. Warsaw University of Technology, Faculty of Chemistry, ul. Noakowskiego 3, 00-664 Warsaw, Poland

Abstract

2-Isoxazolines were obtained from substituted enols or their ester or ether derivatives in 1,3-dipolar cycloaddition reactions with aliphatic or aromatic nitrile oxides.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823403103173967

Reference11 articles.

1. Trihaloacetylated Enol Ethers - General Synthetic Procedure and Heterocyclic Ring Closure Reactions with Hydroxylamine

2. The Reactions of Primary Nitroparaffins with Isocyanates1

3. An improved procedure for the preparation of 2-isoxazolines

4. Nitrile Oxides. V. Stable Aromatic Nitrile Oxides1,2

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4. Utilization of Enols of Mono- and Dicarbonyls Compounds in 1,3-Dipolar Cycloaddition Reactions.;ChemInform;2004-01-20