Diastereoselectivity in the synthesis of D-glycero-D-aldoheptoses by 2-trimethylsilylthiazole homologation from hexodialdo-1,5-pyranose derivatives

DOI: 10.1139/v94-036

Source and publish data:

Canadian Journal of Chemistry p. 237 - 246 (1994)

Update date:2022-09-26

Topics:

Authors:

Khare Khare

Sood Sood

Aspinall

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Article abstract of DOI:10.1139/v94-036

An exploration of the synthesis of D-glycero-D-altro-heptose, a constitutent of O antigen chains in lipopolysaccharides from Campylobacter jejuni serotypes O:23 and O:36 led to a study of the 2-trimethylsilylthiazole homologation procedure for heptose syn

Full text of DOI:10.1139/v94-036

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Product name:Methyl 2,3,4-tri-O-benzyl-α-D-mannohexodialdo-1,5-pyranoside

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