✦ LIBER ✦

A Facile Synthesis of the Phosphoramidites of 2- N -Methyl-2′-deoxy (or 2′-O-allyl)-ψ-isocytidine, 1, 3-Dimethyl-2′-deoxy-ψ-uridine and N 1-Methyl-2′-O-allyl-ψ-uridine as Synthons Suitable for Oligonucleotide Synthesis

✍ Scribed by Bhattacharya, B. K.; Revankar, G. R.

Book ID: 121232095
Publisher: Taylor and Francis Group
Year: 1994
Tongue: English
Weight: 1008 KB
Volume: 13
Category: Article
ISSN: 0732-8311
DOI: 10.1080/15257779408009476

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Nucleosides-126: Selective methylation o

Nucleosides-126: Selective methylation of the C-nucleoside, ψ-isocytidine and its 2$́-deoxy analog. Synthesis of 1-methyl, 3-methyl and 4-o-methyl derivatives

✍ K.W. Pankiewicz; A. Matsuda; K.A. Watanabe; J.J. Fox 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 619 KB

Synthesis of benzyl O-(2-O-methyl-β-d-ga

Synthesis of benzyl O-(2-O-methyl-β-d-galactopyranosyl)-(1→3)-2-acetamido-2-deoxy-β-d-glucopyranoside [benzyl 2′-O-methyllacto-N-bioside I], and its higher saccharide containing an O-(2-O-methyl-β-d-galactopyranosyl)-(1→3)-2-acetamido-2-deoxy-β-d-glucopyranosyl group as a potential substrate for (1→4)-α-l-fucosyltransferase

✍ Arun K. Sarkar; Rakesh K. Jain; Khushi L. Matta 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 1002 KB

Treatment of benzyl O-/?-n-galactopyranosyl-( 1+3)-2-acetamido-2-deoxy-4,6-O-isopropylidene-j3-D-glucopyranoside with tert-butylchlorodiphenylsiiane afforded the 6'-0-tert-butyldiphenylsilyl ether, which was converted into the 3',4'-0-isopropylidene derivative. Methylation and subsequent removal of