Short convergent route to chiral pyrimidine analogues of 2′-deoxy neplanocin A
- 1 January 1990
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 6,p. 458-459
- https://doi.org/10.1039/c39900000458
Abstract
The chiral epoxide (6) has been converted in five stages into the thymidine analogue (14) of Neplanocin A and into the 6′α-(8) and 6′β-(10) hydroxy analogues of carbocyclic Thymidine.Keywords
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