Preparation of trans diequatorial 2,3-pyruvate acetals in a di- and a trisaccharide related to the K-antigen from E. Coli 0101:K103:H-

Article abstract of DOI:10.1080/00397919808006846

Using methyl 2,2-bis(ethylthio)propionate as acetalating agent and triflic acid-sulfuryl chloride as catalyst, synthesis of 2,3-trans diequatorial pyruvate ketal was achieved. Starting from D-galactose and L- rhamnose derivatives, methyl 2,3,4,6-tetra-O-b

Full text of DOI:10.1080/00397919808006846

Synthetic Communications
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
Preparation of trans Diequatorial 2,3-Pyruvate
Acetals in a Di- and a Trisaccharide Related to the
K-Antigen from E. Coli 0101:K103:H−
Anup Kumar Misra , Saibal Kumar Das & Nirmolendu Roy
To cite this article: Anup Kumar Misra , Saibal Kumar Das & Nirmolendu Roy (1998)
Preparation of trans Diequatorial 2,3-Pyruvate Acetals in a Di- and a Trisaccharide Related to
the K-Antigen from E. Coli 0101:K103:H− , Synthetic Communications, 28:8, 1471-1480, DOI:
10.1080/00397919808006846
To link to this article: http://dx.doi.org/10.1080/00397919808006846
Published online: 22 Aug 2006.
Submit your article to this journal
Article views: 21
View related articles
Citing articles: 4 View citing articles
Full Terms & Conditions of access and use can be found at
http://www.tandfonline.com/action/journalInformation?journalCode=lsyc20
Download by: [University of Waterloo]
Date: 26 October 2015, At: 09:28