Acyclonucleoside 류의 합성(2) -2'',3''-disubstituted secouridine의 합성-
Synthesis of Acyclonucleosides (2) -Synthesis of 2'',3''-disubstituted Secouridines-

대한약학회
약학회지
제33권 제5호 (1989년)
1989.10

296 - 299 (4 pages)

The synthetic study of 2'',3''-diazido and difluoro secouridines toward development of new antiviral agents is described. These acyclic nucleosides were synthesized from uridine by the method of ring opening reaction of sugar moiety.

Acyclonucleoside 류의 합성(2) -2'',3''-disubstituted secouridine의 합성-
Synthesis of Acyclonucleosides (2) -Synthesis of 2'',3''-disubstituted Secouridines-

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Acyclonucleoside 류의 합성(2) -2'',3''-disubstituted secouridine의 합성- Synthesis of Acyclonucleosides (2) -Synthesis of 2'',3''-disubstituted Secouridines-

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Acyclonucleoside 류의 합성(2) -2'',3''-disubstituted secouridine의 합성-
Synthesis of Acyclonucleosides (2) -Synthesis of 2'',3''-disubstituted Secouridines-

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