✦ LIBER ✦

Synthesis of seven penta-N,O-acetyl-pseudo-2-amino-2-deoxy-dl-hexopyranoses

✍ Scribed by Seiichiro Ogawa; Masaru Orihara

Book ID: 107725772
Publisher: Elsevier Science
Year: 1988
Tongue: English
Weight: 961 KB
Volume: 177
Category: Article
ISSN: 0008-6215
DOI: 10.1016/0008-6215(88)85053-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of the penta-N,O-acetyl deriva

Synthesis of the penta-N,O-acetyl derivatives of some pseudo-3-amino-3-deoxy-dl-hexopyranoses a and -dl-hexopyranosylamine derivatives

✍ Seiichiro Ogawa; Masaru Orihara 📂 Article 📅 1989 🏛 Elsevier Science 🌐 English ⚖ 585 KB

Proton and carbon-13 n.m.r. spectra of s

Proton and carbon-13 n.m.r. spectra of six pseudo-2-acetamido-2-deoxy-dl-hexopyranoses

✍ Klaus Bock; Seiichiro Ogawa; Masaru Orihara 📂 Article 📅 1989 🏛 Elsevier Science 🌐 English ⚖ 447 KB

Differently N-protected 3,4,6-tri-O-acet

Differently N-protected 3,4,6-tri-O-acetyl-2-amino-2-deoxy-d-glucopyranosyl chlorides and their application in the synthesis of diosgenyl 2-amino-2-deoxy-β-d-glucopyranoside

✍ Bednarczyk, Dorota; Walczewska, Agata; Grzywacz, Daria; Sikorski, Artur; Liberek 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 584 KB

Synthesis of 2-acetamido-2-deoxy-4-O-(2-

Synthesis of 2-acetamido-2-deoxy-4-O-(2-O-methyl-β-D-galactopyranosyl)-d-glucopyranose (N-acetyl-2′-O-methyllactosamine)

✍ Saeed A. Abbas; Conrad F. Piskorz; Khushi L. Matta 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 726 KB

ChemInform Abstract: Synthesis of 1,2,3,

ChemInform Abstract: Synthesis of 1,2,3,4,6-Penta-O-acetyl-5-deoxy-5-phenylphosphonothioyl- D-glucopyranoses.

✍ T. HANAYA; A. AKAMATSU; T. ISONO; H. YAMAMOTO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB

Synthesis of C-glycosides of N-acetylglu

Synthesis of C-glycosides of N-acetylglucosamine by direct alkylation of 2-amino-2-deoxy-2,3,4,6-tetra-O-acetyl glucopyranosyl chloride

✍ Kyung-Il Kim; Rawle I. Hollingsworth 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 156 KB

The B-isomer of C-glycoside, ethyl 2-aceta~no-2-~oxy-3,4,6-~-O-ace~l-~-D-glucopyranosylacetateQ) was prepared stenoselectively in two steps by reaction of 2-acetamino-2-deoxy-3,4X&i-O-acetyl-a-D-glucopyranosyl chloride(&) with potassium diethylmalonate and 18-crown-6, followed by decarboxylation. C-