Carbohydrate research

Studies on the origin of stereoselectivity in the synthesis of 1, 2-trans glycofuranosyl azides

A Štimac, J Kobe

Index: Carbohydrate Research, , vol. 324, # 3 p. 149 - 160

Full Text: HTML

Citation Number: 30

Abstract

... Carbohydrate Research. Volume 324, Issue 3, 25 February 2000, Pages 149–160. Cover image Cover image. ... Glycosyl azides [1] serve as valuable carbohydrate building blocks, especially as precursors to glycosylamines and heterocyclic derivatives such as 1,2,3-triazoles. ...

Related Articles:

Antiviral nucleosides. A stereospecific, total synthesis of 2'-fluoro-2'-deoxy-. beta.-D-arabinofuranosyl nucleosides

[Howell, Henry G.; Brodfuehrer, Paul R.; Brundidge, Steven P.; Benigni, Daniel A.; Sapino, Chester Journal of Organic Chemistry, 1988 , vol. 53, p. 85 - 88]

A stereocontrolled synthesis of 1, 3, 5-tri-O-benzoyl-. alpha.-D-ribofuranose

[Journal of Organic Chemistry, , vol. 50, # 14 p. 2597 - 2598]

6-Methyl-5-azacytidine-synthesis, conformational properties and biological activity. a comparison of molecular conformation with 5-azacytidine

[Hanna, Naeem B.; Zajicek, Jaroslav; Piskala, Alois Nucleosides and Nucleotides, 1997 , vol. 16, # 1-2 p. 129 - 144]

More Articles...