Volume 21, Issue 1
Natural Products
Full Access

ChemInform Abstract: 3-Methylxanthosine: Synthesis and Acidic Hydrolysis of the Glycosyl Bond.

T. ITAYA

T. ITAYA

Fac. Pharm. Sci., Kanazawa Univ., Takara, Kanazawa 920, Japan

Search for more papers by this author
T. HARADA

T. HARADA

Fac. Pharm. Sci., Kanazawa Univ., Takara, Kanazawa 920, Japan

Search for more papers by this author
First published: January 2, 1990

Abstract

3-Methylxanthosine (IVb) is prepared by ethoxycarbonylation of the nucleoside (I) and subsequent base-induced cyclization of the carbamate (III).

ChemInform Abstract

3-Methylxanthosine (IVb) is prepared by ethoxycarbonylation of the nucleoside (I) and subsequent base-induced cyclization of the carbamate (III). Acidic hydrolysis of the N-glycosidic bond in (IVb) proceeds about 1000 times faster than in xanthosine (IVa).

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.