Journal article
Glycosyl disulfides: novel glycosylating reagents with flexible aglycon alteration.
- Abstract:
-
[reaction: see text] Glycosyl disulfides have been shown for the first time to be effective glycosyl donors. Glucosylation and galactosylation of a panel of representative alcohol acceptors allowed the formation of 28 simple glycosides, disaccharides, and glycoamino acids in yields of up to 90%. As well as providing a novel class of effective glycosyl donors, the ability to easily alter the nature of the aglycon and the ability to differently activate donors that differ only in their aglycon ...
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- Publication status:
- Published
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- Publisher copy:
- 10.1021/jo051374j
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Authors
Bibliographic Details
- Journal:
- The Journal of organic chemistry
- Volume:
- 70
- Issue:
- 24
- Pages:
- 9740-9754
- Publication date:
- 2005-11-05
- DOI:
- EISSN:
-
1520-6904
- ISSN:
-
0022-3263
- URN:
-
uuid:801b71b7-d256-4dbc-ba2a-869b3e130a3f
- Source identifiers:
-
52064
- Local pid:
- pubs:52064
Item Description
- Language:
- English
- Keywords:
Terms of use
- Copyright date:
- 2005
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