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A highly convergent synthesis of the phytoalexin elicitor hexasaccharide

A highly convergent synthesis of the elicitor-active D-glucohexatose 1 and its variant 19 was achieved via coupling of the trisaccharide donor 14 with the trisaccharide acceptor 15 followed by deprotection. 14 and 15 were obtained from rearrangement of the orthoesters 6 and 5 respectively which were...

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Bibliographic Details
Published in:Tetrahedron letters 1998-04, Vol.39 (14), p.1937-1940
Main Authors: Wang, W, Kong, F
Format: Article
Language:English
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Summary:A highly convergent synthesis of the elicitor-active D-glucohexatose 1 and its variant 19 was achieved via coupling of the trisaccharide donor 14 with the trisaccharide acceptor 15 followed by deprotection. 14 and 15 were obtained from rearrangement of the orthoesters 6 and 5 respectively which were prepared quantitatively from coupling of the disaccharide 4 with acetobromoglucose and 6-O-chloroacetylated acetobromoglucose respectively. Graphic
ISSN:0040-4039
1873-3581
DOI:10.1016/S0040-4039(98)00087-2