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Stereoselective Transformations in the Thymidine Series

V. Škarić ; Laboratory of Stereochemistry and Natural Products, "Rudjer Boskovic« Institute, 41001 Zagreb, Croatia, Yugoslavia
M. Pavela-Vrančič ; Laboratory of Stereochemistry and Natural Products, "Rudjer Boskovic« Institute, 41001 Zagreb, Croatia, Yugoslavia
J. Matulić-Adamić ; Laboratory of Stereochemistry and Natural Products, "Rudjer Boskovic« Institute, 41001 Zagreb, Croatia, Yugoslavia

Puni tekst: engleski, pdf (5 MB) str. 415-424 preuzimanja: 68* citiraj
APA 6th Edition
Škarić, V., Pavela-Vrančič, M. i Matulić-Adamić, J. (1984). Stereoselective Transformations in the Thymidine Series. Croatica Chemica Acta, 57 (3), 415-424. Preuzeto s https://hrcak.srce.hr/194146
MLA 8th Edition
Škarić, V., et al. "Stereoselective Transformations in the Thymidine Series." Croatica Chemica Acta, vol. 57, br. 3, 1984, str. 415-424. https://hrcak.srce.hr/194146. Citirano 07.03.2021.
Chicago 17th Edition
Škarić, V., M. Pavela-Vrančič i J. Matulić-Adamić. "Stereoselective Transformations in the Thymidine Series." Croatica Chemica Acta 57, br. 3 (1984): 415-424. https://hrcak.srce.hr/194146
Harvard
Škarić, V., Pavela-Vrančič, M., i Matulić-Adamić, J. (1984). 'Stereoselective Transformations in the Thymidine Series', Croatica Chemica Acta, 57(3), str. 415-424. Preuzeto s: https://hrcak.srce.hr/194146 (Datum pristupa: 07.03.2021.)
Vancouver
Škarić V, Pavela-Vrančič M, Matulić-Adamić J. Stereoselective Transformations in the Thymidine Series. Croatica Chemica Acta [Internet]. 1984 [pristupljeno 07.03.2021.];57(3):415-424. Dostupno na: https://hrcak.srce.hr/194146
IEEE
V. Škarić, M. Pavela-Vrančič i J. Matulić-Adamić, "Stereoselective Transformations in the Thymidine Series", Croatica Chemica Acta, vol.57, br. 3, str. 415-424, 1984. [Online]. Dostupno na: https://hrcak.srce.hr/194146. [Citirano: 07.03.2021.]

Sažetak
The s tereoselective 5% Rh/ AliOa hydrogenations Olf .thymidine,
3',5'-anhydro- X and 3'-deoxy- XII thymidines to -the
corresipondiing (5S) - 5,6-d1hydirothymi!di..ne deirivaitiv1es I, IX, and
XIII were evLdenced by 1H- and 13C-NMR analyses and N-.glycosidix!
bo1I1d cleaV'ages .to (-)-S-5,6-dihydrot:hymine. Th:e regiose
·lect.ive syntiheses 01f the configuraotionally defined (58)-5'-
0-tosyl- (Ill) and (5'S)-5'-deoxy-5'-iodo- (IV) 5,6-dihydrothymidines
aire descriibed. The tntramolecular cyC'lisat.ion of (5S) - 3',5'-dimesyloxy-5,6- -dihydrothymidine (II) by NaiOMe afforded (5R,5S)-5'-0-mesy.I- -2,3' -anhydro- 5,6-dihydrothym.idines 5,6-Dihydropyrimidine

Hrčak ID: 194146

URI
https://hrcak.srce.hr/194146

Posjeta: 122 *