alpha-Thymidine (4) was synthesized from thymidine (1) in 3 steps in 3
6% overall yield without using chromatography and with the possibility
of increasing the yield to 85% by reusing the remaining alpha,beta-mi
xture. O-p-toluoyl-alpha-D-erythro-pentofuranosyl)thymine (3) was furt
her converted to y-alpha-D-erythro-pentofuranosyl)-5-methylcytosine (5
).