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Synthesis of a <i>C</i>‑Glycoside Analogue of β‑Galactosyl Ceramide, a Potential HIV‑1 Entry Inhibitor
https://doi.org/10.1021/jo402115w.s001
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journal contribution
posted on 2013-12-06, 00:00
authored by
V. Narasimharao Thota
,
Mula Brahmaiah
,
Suvarn S. Kulkarni
A β-<i>C</i>-galactosyl ceramide was synthesized in a stereoselective manner, employing a Sharpless AD reaction and olefin cross metathesis as key steps.
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Synthesis of a <i>C</i>‑Glycoside Analogue of β‑Galactosyl Ceramide, a Potential HIV‑1 Entry Inhibitor
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Categories
Biochemistry
Microbiology
Cell Biology
Molecular Biology
Neuroscience
Biotechnology
Chemical Sciences not elsewhere classified
Information Systems not elsewhere classified
Mental Health
Keywords
ceramide
metathesi
Potential
Galactosyl
HIV
olefin
InhibitorA
Synthesi
stereoselective manner
Entry
Ceramide
Sharpless AD reaction
Analogue
Licence
CC BY-NC 4.0
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