A Convenient Method for C-Azanucleosides Synthesis
…, T Akiba, Y Ochiai, A Momotake, H Togo
Index: Yokoyama, Masataka; Akiba, Takahiro; Ochiai, Yoshie; Momotake, Atsuya; Togo, Hideo Journal of Organic Chemistry, 1996 , vol. 61, # 17 p. 6079 - 6082
Full Text: HTML
Citation Number: 25
Abstract
As a part of our program for synthesis and evaluation of the C-nucleosides as a new type of DNA unit, 1 we have been interested in the C-azanucleosides in which the endocyclic ribosyl ring oxygen is replaced with a nitrogen atom. To our knowledge, many modified nojirimycins, which function as effective glycosidase inhibitors, have been reported, 2 and only three C-azanucleosides3 have been synthesized as nojirimycin analogs. However, ...
Related Articles:
A Convenient Method for C-Azanucleosides Synthesis
[Journal of Organic Chemistry, , vol. 61, # 17 p. 6079 - 6082]
Synthesis of 2-substituted pyrrolidines from nitriles
[Tetrahedron Letters, , vol. 54, # 37 p. 5001 - 5003]