A NOVEL REGIO- AND HIGHLY STEREOSELECTIVE ANOMERIC DEACETYLATION OF 2-AMINOSUGAR DERIVATIVES.

DOI: 10.1016/S0040-4039(00)91795-7

Source and publish data:

Tetrahedron Letters p. 1359 - 1362 (1993)

Update date:2022-09-26

Topics:

Authors:

Avalos, Martin

Babiano, Reyes

Cintas, Pedro

Jimenez, Jose L.

Palacios, Juan C.

Valencia, Concepcion

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Article abstract of DOI:10.1016/S0040-4039(00)91795-7

Silica gel-mediated anomeric deacetylation of per-acetylated 2-amino-2-deoxy-glycopyranose derivatives in methanol constitutes a mild and inexpensive protocol for the selective deprotection of these relevant carbohydrate templates.The reaction proceeds wi

Full text of DOI:10.1016/S0040-4039(00)91795-7

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Article Doi

A NOVEL REGIO- AND HIGHLY STEREOSELECTIVE ANOMERIC DEACETYLATION OF 2-AMINOSUGAR DERIVATIVES.

DOI: 10.1016/S0040-4039(00)91795-7

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)91795-7

Full text of DOI:10.1016/S0040-4039(00)91795-7

Products guided by the article

R&D Labs maybe for 148943-80-0

Relevant to this article

Hydrogen bonding or stacking interactions in differentiating duplex stability in oligonucleotides containing synthetic nucleoside probes for alkylated DNA

The Reaction of Nitrones with (R)-(+)-Methyl p-Tolyl Sulfoxide Anion; Asymmetric Synthesis of Optically Active Secondary Amines

Synthesis of functionalized acetophenones by formal [3+3] cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes with 3-alkoxyand 3-silyloxy-2-acetyl-2-en-1-ones

Silylstannations of α,β-unsaturated carbonyl compounds via the generation of Bu3Sn- in ionic liquids

1β-methyl-2-(5-substituted pyrrolidin-3-ylthio)carbapenems; 3. Synthesis and antibacterial activity of BO-2727 and its related compounds

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