(Q63198334)

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Diels-alder reaction of 2′,3′-unsaturated-3′-nitro-thymidine. First chemical evidence of nitroxide radical formation in the radical-promoted denitration reaction

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Diels-alder reaction of 2′,3′-unsaturated-3′-nitro-thymidine. First chemical evidence of nitroxide radical formation in the radical-promoted denitration reaction (English)

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Jyoti Chattopadhyaya

4

object named as

J. Chattopadhyaya

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author name string

N. Hossain

1

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J. Plavec

2

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C. Thibaudeau

3

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publication date

January 1993

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49

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40

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9079-9088

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New synthesis of 2',3'-dideoxy-3'-C-cyano-2'-substituted thymidines by michael addition reactions

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New syntheses of 2',3'-dideoxy-2',3'-di-substituted & -2'-mono-substituted uridines & adenosines by michael addition reactions

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Michael addition reactions of α β-ene-3′-phenylselenone of uridine. New synthesis of 2′,3′-dideoxy-ribo-aziridino-, 2′,3′-dideoxy-2′, 3′-ribo-cyclopropyl- & 2,2′-O-anhydro-3′-deoxy-3′-amino uridine derivatives

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Synthesis of new 2',3'-dideoxy-2',3'-α-fused-heterocyclic uridines, & some 2', 3'-ene-2'-substituted uridines from easily accessible 2',3'- ene-3'phenylselenonyl uridine

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Conjugated nitroalkenes: versatile intermediates in organic synthesis

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Intramolecular [4+2]-cycloadditions of nitroalkenes with olefins. 2

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Nitroethylene: a stable, clean, and reactive agent for organic synthesis

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Identifiers

10.1016/S0040-4020(01)91224-4

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