1,3-Dipolar cycloadditions: part XIV – Highly selective cycloadditions of C, N-diaryl nitrones to diethyl aryl methylene malonates¹
IR@NISCAIR: CSIR-NISCAIR, New Delhi - ONLINE PERIODICALS REPOSITORY (NOPR)
View Archive Info| Field | Value | |
| Creator |
Banerji, A
Sengupta, S Nayak, A Biswas, P K Bhattacharya, B S Dasgupta, (Mrs. Ray) Saha, R Prange, Thierry Neuman, Alain |
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| Date |
2008-04-03T09:17:57Z
2008-04-03T09:17:57Z 2007-09 |
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| Identifier |
0376-4699
http://hdl.handle.net/123456789/688 |
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| Description |
1495-1500
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. |
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| Language |
en_US
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| Publisher |
CSIR
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| Source |
IJCB Vol.46B(9) [September 2007]
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| Subject |
1,3-Dipolar cycloadditions
Nitrones Cycloadducts Aryl methylene malonates Dipolarophile |
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| Title |
1,3-Dipolar cycloadditions: part XIV – Highly selective cycloadditions of C, N-diaryl nitrones to diethyl aryl methylene malonates¹
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| Type |
Article
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