Tetrasubstituted N-Azolyl Olefins via Products from Sequential SRN1 Reactions

R. Beugelmans; A. Lechevallier; T. Frinault; T. Gharbaoui; R. Benhida

doi:10.1055/s-1994-22909

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Synlett 1994; 1994(7): 513-514
DOI: 10.1055/s-1994-22909

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Tetrasubstituted N-Azolyl Olefins via Products from Sequential S_RN1 Reactions

R. Beugelmans^* , A. Lechevallier, T. Frinault, T. Gharbaoui, R. Benhida

^*Institut de Chimie des Substances Naturelles, C.N.R.S., 91198 Gif-sur-Yvette, France

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Publication Date:
18 September 2002 (online)

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The synthesis of new N-azolyl (N9-adenine; 4-nitroimidazole) tetrasubstituted and functionalized olefins is based upon Grob type fragmentation or E_RC1 elimination reactions carried out on products obtained by two sequential S_RN1 reactions.

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