Indrasena Reddy, T. ; Bhawal, Baburao M. ; Rajappa, Srinivasachari (1993) Unique zeolite-catalyzed synthesis of nitroketene S,N-acetals Tetrahedron, 49 (10). pp. 2101-2108. ISSN 0040-4020
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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...
Related URL: http://dx.doi.org/10.1016/S0040-4020(01)86309-2
Abstract
Dimethyl carbonimidodithioates (4a-g, 7a-c) derived from various primary amines and amino acid esters [glycine, (L)-alanine and (L)-phenylalanine] have been condensed with nitromethane in the presence of the rare-earth exchanged zeolite RE(70%)Na Y to give the S,N-acetals (5a-g, 8a-c). Mercuric chloride catalyzed hydrolysis of these (8a-c) has led to the nitroacetyl derivatives (9a-c). The glycine derivative (7a) gives a dimeric product (11) when heated alone with the zeolite.
Item Type: | Article |
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Source: | Copyright of this article belongs to Elsevier Science. |
ID Code: | 50330 |
Deposited On: | 23 Jul 2011 07:19 |
Last Modified: | 23 Jul 2011 07:19 |
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