Synthesis and utility of new amine/nucleobase addition products of allenylphosphonates

Kumara Swamy, K. C. ; Balaraman, E. ; Satish Kumar, N. (2006) Synthesis and utility of new amine/nucleobase addition products of allenylphosphonates Tetrahedron, 62 (43). pp. 10152-10161. ISSN 0040-4020

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

Related URL: http://dx.doi.org/10.1016/j.tet.2006.08.034

Abstract

In the reaction of allenylphosphonates with amines/nucleobases, depending on the amine and the allenylphosphonate, either Z- or E-vinylphosphonate or allylphosphonate as a single isomer with a β-amino functionality was isolated. A simple route to phosphonates with a β-NH2 group is developed by direct reaction with ammonia. In reactions with adenine, three different modes of reaction, with one of them involving an unusual cyclisation, are observed. The utility of (enamino)allyl phosphonate products thus obtained in the synthesis of (enamino)-1,3-butadienes via Horner-Wadsworth-Emmons (HWE) reaction is also demonstrated.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Allenylphosphonates; Nucleobase; Enaminophosphonates; HWE Reaction; Mitsunobu Reaction; X-ray Structure
ID Code:29658
Deposited On:23 Dec 2010 05:40
Last Modified:17 May 2016 12:28

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