Header menu link for other important links
X
1,3-Dipolar cycloadditions: Part XIV - highly selective cycloadditions of C, N-diaryl nitrones to diethyl aryl methylene malonates
A BANERJI, S SENGUPTA, A NAYAK, P K BISWAS, B BHATTACHARYA, S DASGUPTA, R SAHA, T PRANGE, A NEUMAN
Published in -
2007
Volume: 46
   
Issue: 9
Pages: 1495 - 1500
Abstract
Cycloaddition of nitrones to diethyl arylmethylene malonates occurred with very high selectivity to furnish 3,5-trans-2,3,5-triaryl-4,4-dicarbethoxy isoxazolidines. This is in contrast with the nitrone cycloadditions to other α,β-conjugated carbonyl derivatives where two diastereoisomeric (and on occasion regioisomeric) cycloadducts are generally obtained.
About the journal
JournalIndian Journal of Chemistry - Section B Organic and Medicinal Chemistry
Publisher-
ISSN0376-4699