Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/688
Title: 1,3-Dipolar cycloadditions: part XIV – Highly selective cycloadditions of C, N-diaryl nitrones to diethyl aryl methylene malonates¹
Authors: Banerji, A
Sengupta, S
Nayak, A
Biswas, P K
Bhattacharya, B
S Dasgupta, (Mrs. Ray)
Saha, R
Prange, Thierry
Neuman, Alain
Keywords: 1,3-Dipolar cycloadditions
Nitrones
Cycloadducts
Aryl methylene malonates
Dipolarophile
Issue Date: Sep-2007
Publisher: CSIR
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.
Description: 1495-1500
URI: http://hdl.handle.net/123456789/688
ISSN: 0376-4699
Appears in Collections:IJC-B Vol.46B(09) [September 2007]

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