78795-27-4Relevant articles and documents
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
Carbocyclic Analogs of Thymine Nucleosides and Related 1-Substituted Thymines
Shealy, Y.Fulmer,O'Dell, C.Allen,Thorpe, Martha C.
, p. 383 - 389 (2007/10/02)
The carbocyclic analogs of thymidine (IXf), 1-β-ribofuranosylthymine (IXg), and 1-β-3'-deoxyribofuranosylthymine (IXe) were synthesized by incorporating modifications into the Shaw method of synthesizing 2,4-(1H,3H)pyrimidinediones via acryloylureas.Simpler analogs of thymine nucleosides were also prepared by this method.The carbocyclic analog of thymidine displayed modest activity against Leukemia L1210 in vivo.It differs from a compound prepared previously by a Prins reaction.