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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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Published in: | Tetrahedron letters 1998-04, Vol.39 (14), p.1937-1940 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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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.
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/S0040-4039(98)00087-2 |