Bulletin of the Chemical Society of Japan

The Convenient Synthesis of Anhydronucleosides via the 2′, 3′-O-Sulfinate of Pyrimidine Nucleosides as the Active Intermediates

T Sowa, K Tsunoda

Index: Bulletin of the Chemical Society of Japan, , vol. 48, p. 505 - 507

Full Text: HTML

Citation Number: 32

Abstract

Page 1. February, 1975] BULLETIN Of THÉ CHEHÖCAL SOCfËTV OÍ JAPAN, VOL. ... Anhydronucleosides are important modifications of natural nucleosides and have been used as intermediates in the chemical synthesis of arabinonucleosides. ...

Related Articles:

Reactions of 2-acyloxyisobutyryl halides with nucleosides. V. Reactions with cytidine and its derivatives

[Journal of Organic Chemistry, , vol. 39, # 15 p. 2182 - 2186]

An efficient synthesis of 1-. beta.-D-arabinofuranosylcytosine

[Journal of Organic Chemistry, , vol. 41, # 10 p. 1828 - 1831]

2, 2'-Anhydropyrimidine nucleosides. Novel syntheses and reactions

[Journal of Organic Chemistry, , vol. 38, # 3 p. 593 - 598]

Vilsmeier-Haack reaction. IV. Convenient synthesis of 2, 2'-anhydro-1-. beta.-D-arabinofuranosyl cytosine (2, 2'-cyclocytidine) and its derivatives

[Journal of Organic Chemistry, , vol. 37, p. 284 - 288]

An efficient synthesis of 1-. beta.-D-arabinofuranosylcytosine

[Journal of Organic Chemistry, , vol. 41, # 10 p. 1828 - 1831]

More Articles...