A novel and versatile glycosyl donor for the preparation of glycosides of N-acetylneuraminic acid

DOI: 10.1016/S0040-4039(98)00359-1

Source and publish data:

Tetrahedron Letters p. 3065 - 3068 (1998)

Update date:2022-08-03

Topics:

Authors:

Demchenko, Alexei V.

Boons, Geert-Jan

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(98)00359-1

An N-diacetyl derivative of neuraminic acid exhibits excellent glycosyl donor properties and is a very useful substrate for the preparation of glycosides of N-acetylneuraminic Acid. The donor will be a key component in the preparation of a heptasaccharide derived from group B type III Streptococcus.

Full text of DOI:10.1016/S0040-4039(98)00359-1

Products guided by the article

Product name:(2S,4S,5R,6R)-4-Acetoxy-5-acetylamino-2-[(2R,3S,4S,5R,6R)-3,5-diacetoxy-2-benzoyloxymethyl-6-(2-trimethylsilanyl-ethoxy)-tetrahydro-pyran-4-yloxy]-6-((1S,2R)-1,2,3-triacetoxy-propyl)-tetrahydro-pyran-2-carboxylic acid methyl ester

Cas No:121360-17-6

R&D Labs maybe for 121360-17-6

Kaiping Genuine Biochemical Pharmaceutical Co.,Ltd.

Contact:+86-750-2881198

Address:No.1, Xinke Road, Shatang Town, Kaiping, Guangdong Province, P.R.China
PharmOrgsyn

Contact:+86-21-38228826

Address:Room 505 Building 2, No 3377 Kangxin Highway, Shanghai, Republic China
taizhou creating bio-pharm co.,ltd.

Contact:+86- 576- 88827176

Address:715 room ,unit A.junyue Building,Jiaojiang,Taizhou,Zhejiang,China
GenicBio Limited

Contact:+86-(0)21-3770 9035

Address:Room 301, Building 2, Meijiabang Road 1508, Shanghai China
Heliosense Biotechnologies, Inc.

website:https://www.heliosense.com/

Contact:+86-592-5667290

Address:Xiamen Torch Hi-tech Zone Venture Weiye Building S506

Relevant to this article

Synthesis and studies of hydrolysis of p-nitrophenyl picolinate catalysed by schiff base zinc (ii) complexes with aza-crown ether or morpholinopendants

Doi:10.3184/030823409X450525
(2009)
Highly enantioselective aldol reaction of acetaldehyde and isatins only with 4-hydroxydiarylprolinol as catalyst: concise stereoselective synthesis of (R)-convolutamydines B and E, (-)-donaxaridine and (R)-chimonamidine

Doi:10.1016/j.tet.2009.12.041
(2010)
Cyclization of propargylic amides: Mild access to oxazole derivatives

Doi:10.1002/chem.200902472
(2010)
Fluoro- and nitro-substitution effect of some chiral compounds

Doi:10.1080/15421400802406463
(2008)
Synthesis of α-Chlorolactams by Cyanoborohydride-Mediated Radical Cyclization of Trichloroacetamides

Doi:10.1002/chem.201800210
(2018)
K₃PO₄-catalyzed regiospecific aminobromination of βnitrostyrene derivatives with N-Bromoacetamide as aminobtominating agent

Doi:10.1021/jo9026879
(2010)

Article Doi