116856-49-6Relevant articles and documents
Synthesis of the two enantiomers of the carbocyclic analog of nicotinamide ribose and analysis of their biological properties
Ikbal,Cerceau,Le Goffic,Sicsic
, p. 415 - 420 (1989)
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Synthesis of carbocyclic nucleosides from 2-azabicyclo[2.2.1]hept-5-en-3-ones: Sodium borohydride-mediated carbon-nitrogen bond cleavage of five- and six-membered lactams
Katagiri,Muto,Nomura,Higashikawa,Kaneko
, p. 1112 - 1122 (2007/10/02)
Various carbocyclic ribofuranosyl nucleosides were stereoselectively synthesized through a small number of steps from 2-azabicyclo[2.2.1]hept-5-en-3-ones by the use of sodium borohydride-mediated C-N bond cleavage as a key step. Ready availability of a no