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C‐glycosides III. Cyclo‐additions dipolaires ‐ 1,3 d'oxydes de nitriles et de nitrilimines. Communication préliminaire
Author(s) -
Tronchet J. M. J.,
Jotterand A.,
Le Hong N.,
Perret Melle F.,
ThorndahlJaccard Mme S.,
Tronchet Mme J.,
Chalet J. M.,
Faivre Melles L.,
Hausser C.,
Sébastian C.
Publication year - 1970
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19700530631
Subject(s) - chemistry , glycosyl , cycloaddition , glycoside , stereochemistry , organic chemistry , catalysis
1.3‐dipolar cycloaddition of alkenes (or alkynes) on sugars‐nitriloxides and nitrilimines led respectively to 3‐glycosyl‐isoxazolines (or isoxazoles) and 3‐glycosyl‐pyrazolines (or pyrazoles). 5‐glycosyl‐isoxazolines were similarly prepared from arylnitriloxides and α‐ or ω‐unsaturated sugars. These new C‐glycosides are potential antiviral and anti‐tumor agents.