✦ LIBER ✦

Synthesis of 2-acetamido-2,4-dideoxy-4-fluoro-3-O-β-d-galactopyranosyl-d-glucopyranose. A potential specific substrate for (1→2)-α-l-fucosyltransferase

✍ Scribed by Rexford L. Thomas; Saeed A. Abbas; Conrad F. Piskorz; Khushi L. Matta

Publisher: Elsevier Science
Year: 1988
Tongue: English
Weight: 353 KB
Volume: 175
Category: Article
ISSN: 0008-6215
DOI: 10.1016/0008-6215(88)80167-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of O-α-l-fucopyranosyl-(1→3)-O

Synthesis of O-α-l-fucopyranosyl-(1→3)-O-β-d-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-d-glucopyranose (N-acetyl-3′-O-α-l-fucopyranosyllactosamine)

✍ Raschmi Dubey; Donna Reynolds; Saeed A. Abbas; Khushi L. Matta 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 590 KB

A facile synthesis of benzyl 2-acetamido

A facile synthesis of benzyl 2-acetamido-6-O-acetyl-4-O-(6-O-acetyl-3,4-O-isopropylidene-β-d-galactopyranosyl)-2-deoxy-β- d-glucopyranoside, a key intermediate for the synthesis of O-α-l-fucopyranosyl-(1→2)-O-β-d-galactopyranosyl-(1→4)-O-[α-l-fucopyranosyl- (1→3)]-2-acetamido-2-deoxy-d-glucopyranose

✍ Surjit S. Rana; Khushi L. Matta 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 269 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

A convenient synthesis of O-α-l-fucopyra

A convenient synthesis of O-α-l-fucopyranosyl-(1 → 2)-O-β-d-galactopyranosyl-(1 → 4)-d-glucopyranose (2′-O-α-l-fucopyranosyllactose)

✍ Rakesh K. Jain; Robert D. Locke; Khushi L. Matta 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 293 KB

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

Synthesis of methyl O-(2-O-methyl-β-d-galactopyranosyl)-(1 → 4)-O-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-(1 → 3)- β-d-galactopyranoside and 4-nitrophenyl O-β-d-galactopyranosyl-(1 → 4)-O-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-(1 → 3)-β-d-galactopyranoside

✍ Shaheer H. Khan; Rakesh K. Jain; Khushi L. Matta 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 704 KB

Recent years have seen a remarkable surge of interest in the study of U-Lfucosyltransferases. Of these L-fucosyltransferases, the enzyme (143)~a+fucosyltransferase has attracted a great deal of clinical interest as a potential tumor marker. This enzyme catalyzes the transfer of an L-fucosyl group f

A synthesis of 8-methoxycarbonyloct-1-yl

A synthesis of 8-methoxycarbonyloct-1-yl O-α-d-galactopyranosyl-(1→3)-O-β-d-galactopyranosyl-(1→4)-2-acetamido-2-deoxy-β-d-glucopyranoside

✍ Per J. Garegg; Stefan Oscarson 📂 Article 📅 1985 🏛 Elsevier Science 🌐 English ⚖ 480 KB

Halide-assisted glycosyIation, using a non-p~icipating Z-substituent (benzyl) in the glycosyl halide, was used to obtain the ~-D-gaiactosyl linkage and silver triflate promotion with a participating 2-substituent (benzoyl) was used to obtain the /3-D-galactosyl linkage in a facile synthesis of the t