This submission belongs to the session a. General Organic Synthesis of the event The 3rd International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 1999
Citation
T. Tejero, S. Anoro, F. L. Merchan, P. Merino, 1,3-Dipolar Cycloadditions of N-Benzyl Furfuryl Nitrones to Vinyl Ethers and a,b-Unsatureted Esters, in Proceedings of The 3rd International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 1999, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-3-01718
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1,3-Dipolar Cycloadditions of N-Benzyl Furfuryl Nitrones to Vinyl Ethers and a,b-Unsatureted Esters
T. Tejero 1
S. Anoro 1
F. L. Merchan 1
P. Merino 1
1. Laboratorio de Sintesis Asimetrica, Departamento de Quimica Organica, Facultad de Ciencias-ICMA, Universidad de Zaragoza-CSIC, E-50009 Zaragoza, Aragon, Spain
Abstract
While abundant information on the reactivity of several classes of nitrones exists [1], hetaryl nitrones, i.e. nitrones bearing an heterocyclic ring at the carbon atom, have been the subject of very few investigations [2]. Recent publications from our laboratory have been concerned with the use of thiazolyl nitrones 1 as a suitable substrate for both nucleophilic additions [3] and 1,3-dipolar cycloadditions [4]. Our continued interest in the reactivity of hetaryl nitrones has led to investigate the reaction of the furfuryl nitrones 2 with several alkenes. In this communication we report our preliminary results on this topic.
Keywords
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