Chemical and Pharmaceutical Bulletin p. 1601 - 1603 (1995)
Update date:2022-08-04
Topics: Characterization Optimization Purification Protection of Functional Groups Starting Material Scale-up De-Protection Functional Group Modifications
Inaba
Inami
Kimoto
Yanada
Miwa
Taga
Bessho
The stereospecific synthesis is described of the first member of a new class of C-nucleoside analogues in which the sugar ring is replaced with a 1,3-thiazolidine ring. The 1,3-thiazolidin-2-yl analogues (1) and (2) of pseudouridine were prepared stereospecifically via condensation of L or D- cysteine with a formylated nucleobase.
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Doi:10.1021/om950528q
(1996)Doi:10.1016/0040-4039(95)01857-E
(1995)Doi:10.1016/0022-328X(95)05498-E
(1995)Doi:10.1107/S0108270195009899
(1996)Doi:10.1016/0223-5234(96)88309-7
(1995)Doi:10.1016/0584-8539(71)80155-1
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