Nucleosides and Nucleotides p. 683 - 685 (1999)
Update date:2022-08-05
Topics:
Messini, Lea
Tiwari, Kamal N.
Montgomery, John A.
Secrist III, John A.
Coupling of 1-O-acetyl-2-deoxy-3,5-di-O-toluoyl-4-thio-D-ribofuranose with 6-chloropurine and 2,6-dichloropurine gave a mixture of 9α and 9β anomers as major products. These anomers were separated and converted to 2′-deoxy-4′-thio analogues of adenosine, inosine, guanosine, 2-amino-adenosine, and 2-chloro adenosine as well as their α-anomers. Copyright
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