Syntheses of peptidoglycolipid analogs with distinct immunomodulating activities

Article abstract of DOI:10.1080/07328300008544102

Amphiphilic 2-amino-2-deoxy-β-D-glucopyranosylamides were synthesized from N-protected glucosamine derivatives via N-glycosidation with fatty amines, subsequent N-acylation with fatty acid derivatives and deprotection. They could further be modified with

Full text of DOI:10.1080/07328300008544102

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Journal of Carbohydrate Chemistry
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Syntheses of Peptidoglycolipid
Analogs with Distinct
Immunomodulating Activities
Oswald Lockhoff & Yutaka Hayauchi
a Bayer AG, Central Research , ZF-WF Q18, D-51368
Leverkusen, Germany
Published online: 07 Mar 2008.
To cite this article: Oswald Lockhoff & Yutaka Hayauchi (2000) Syntheses of Peptidoglycolipid
Analogs with Distinct Immunomodulating Activities, Journal of Carbohydrate Chemistry,
19:4-5, 603-619, DOI: 10.1080/07328300008544102
To link to this article: http://dx.doi.org/10.1080/07328300008544102
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