Direct conversion of 2-acetamido-2-deoxysugars to 1,2-oxazoline derivatives by dehydrative cyclization in water

Heterocycles

Volumn 63, Issue 7, 2004, Pages 1531-1535

  Kadokawa, Jun Ichi ^a   Mito, Mitsumasa ^a   Takahashi, Satoshi ^a   Noguchi, Masato ^a   Shoda, Shin Ichiro ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1,2 OXAZOLINE DERIVATIVE; 2 ACETAMIDO 2 DEOXYSUGAR; CHITIN DERIVATIVE; CYANAMIDE; GLYCOSIDASE; LEWIS ACID; N ACETYLGALACTOSAMINE; N ACETYLGLUCOSAMINE; N,N' DIACETYLCHITOBIOSE; OXAZOLINE DERIVATIVE; SUGAR OXAZOLINE DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ACETYLATION; ARTICLE; CHEMICAL BOND; CYCLIZATION; DEHYDRATIVE CYCLIZATION; ENZYME GLYCOSYLATION; ENZYME MECHANISM; GLYCOSIDIC BOND; METABOLISM; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME; STEREOCHEMISTRY;

EID: 3142550532     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-04-10065     Document Type: Article

References (23)

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23. 1HNMR spectrum of the reaction mixture indicated that in the α- and β-anomers, β-anomer predominantly reacted with WSC-HCl, because the ratio of the peak due to β-anomeric proton decreased with progress of the reaction.