88095-33-4Relevant articles and documents
Sc(OTf)3-catalyzed C-glycosidation of glycals: A facile synthesis of allyl glycosides, glycosyl cyanides and glycosyl azides
Yadav,Reddy,Chand, Pratap K
, p. 4057 - 4059 (2001)
The treatment of glycals with allyltrimethylsilane, trimethylsilyl cyanide and trimethylsilyl azide in the presence of catalytic amounts of Sc(OTf)3 gave the corresponding 2,3-unsaturated allyl glycosides, glycosyl cyanides and glycosyl azides in excellent yields with high α-selectivity.
SYNTHESIS OF C-GLYCOSYL COMPOUNDS FROM 3,4,6-TRI-O-ACETYL-1,5-ANHYDRO-D-arabino-HEX-1-ENITOL AND ALLYLTRIMETHYLSILANE AND BIS(TRIMETHYLSILYL)ACETYLENE
Ichikawa, Yoshiyasu,Isobe, Minoru,Konobe, Masato,Goto, Toshio
, p. 193 - 200 (2007/10/02)
C-glycosyl derivatives of compounds bearing two, three, or four carbon atoms were obtained from 3,4,6-tri-O-acetyl-1,5-anhydro-D-arabino-hex-1-enitol (1) via a deacetoxylated oxonium ion generated by treatment with a Lewis acid.The nucleophilic reagents w
REACTION OF 4,6-O-BENZYLIDENE-3-O-MESYL-ALLAL WITH ALLYLIC GRIGNARD REAGENTS. HIGHLY REGIO- AND STEREOSELECTIVE PREPARATION OF 2,6-DISUBSTITUTED DIHYDROPYRAN RINGS
Ogihara, Takuo,Mitsunobu, Oyo
, p. 3505 - 3508 (2007/10/02)
The reaction of 4,6-O-benzylidene-1,2-dideoxy-3-O-mesyl-D-ribo-hex-1-enopyranose reacted with 2-propenylmagnesium chloride or 2-methyl-2-propenylmagnesium chloride to give 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-1-C-prop-2-enyl- (or 2-methylprop-2-enyl)-β-D-erythro-hex-2-enitol in good yield.