✦ LIBER ✦

Reactions of furanoside epoxides. The preparation of bromohydrins from methyl 5-O-acetyl-2,3-anhydro-α (and β)-D-ribofuranoside

✍ Scribed by Elmer J. Reist; Sandra L. Holton

Book ID: 108308238
Publisher: Elsevier Science
Year: 1969
Tongue: English
Weight: 573 KB
Volume: 9
Category: Article
ISSN: 0008-6215
DOI: 10.1016/s0008-6215(00)82890-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Syntheses and React

ChemInform Abstract: Syntheses and Reactions of 5-O-Acetyl-1,2-anhydro-3-O-benzyl-α-D-ribofuranose and -β-D-lyxofuranose, 5-O-Acetyl-1,2-anhydro-3,6-di-O-benzyl- and 1,2-Anhydro-5,6-di-O-benzoyl-3-O-benzyl-β-D-mannofuranose, and 6-O-Acetyl-1,2-anhydro-3,4-di-O-benzyl-α-D-glucopyranose and -β-D-talopyranose.

✍ Jun Ning; Fanzuo Kong 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 44 KB 👁 2 views

ChemInform Abstract: Preparation of Meth

ChemInform Abstract: Preparation of Methyl 2,3-Anhydro- and 2,3-O-Sulfinylfuranosides from Unprotected Furanosides Using the Mitsunobu Reaction.

✍ Oliver Schulze; Juergen Voss; Gunadi Adiwidjaja 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Synthesis and mass spectra of 4-O-acetyl

Synthesis and mass spectra of 4-O-acetyl-1,5-anhydro-2,3,6-tri-O-ethyl-d-glucitol and the positional isomers of 4-O-acetyl-1,5-anhydro-di-O-ethyl-O-methyl-d-glucitol and 4-O-acetyl-1,5-anhydro-O-ethyl-di-O-methyl-d-glucitol

✍ Samuel G. Zeller; Anello J. D'Ambra; Michael J. Rice; Gary R. Gray 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 657 KB

Synthesis and mass spectra of 4-O-acetyl

Synthesis and mass spectra of 4-O-acetyl-1,5-anhydro-2,3,6-tri-O-(methoxycarbonylmethyl)-d-glucitol and the positional isomers of 4-O-acetyl-1,5-anhydro-di-O-(methoxycarbonylmethyl)-O-methyl-d-glucitol and 4-O-acetyl-1,5-anhydro-O-(methoxycarbonylmethyl)di-O-methyl-d-glucitol

✍ Samuel G. Zeller; George W. Griesgraber; Gary R. Gray 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 765 KB

Reductive cleavage of fully methylated, partially O-carboxymethylated cellulose had previously been shown to produce 4-O-acetyl-1,5-anhydro-2,3,6-tri-O-methyl-, -2-O-(methoxycarbonylmethyl)-3,6-di-O-methyl-, -3-O-(methoxycarbonylmethyl)-2,6-di-O-methyl-, -6-O-(methoxycarbonylmethyl)-2,3-di-O-methyl-

Reinvestigation of the synthesis of β-d-

Reinvestigation of the synthesis of β-d-ribofuranosyl β-d-ribofuranoside from 1-O-acetyl-2,3,5-tri-O-benzoyl-β-d-ribofuranose using boron trifluoride etherate

✍ Leon M. Lerner 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 349 KB

Stereochemical control of the glycosylat

Stereochemical control of the glycosylation reaction via 3,5-di-O-(p-toluoyl)-2-O-(p-toluolsulfonyl)-β-D-methyl ribofuranoside

✍ Christos Papageorgiou; Christoph Tamm 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 195 KB

Lewis acid catalyzed glycosylation of the 2'-tosyl ribofuranose derivative jj leads exclusively to fi-nucleosides in the uridine and adenosine series.