119125-07-4Relevant academic research and scientific papers
PREPARATION OF METHYL 4,6-O-BENZYLIDENE-2-CHLORO- AND -2-BROMO-α- AND β-D-xylo-HEXOPYRANOSID-3-ULOSES AND THEIR α-D-ribo ISOMERS, AND FORMATION OF GLYCOSID-3-ULOSE HYDRATES FOR THE β-D-xylo ISOMERS
Sakakibara, Tohru,Nakagawa, Toshio
, p. 231 - 242 (2007/10/02)
The title glycosid-3-uloses were prepared from 3-nitro-β-D-threo-hex-2-eno-pyranoside derivatives. 1H-N.m.r. spectral studies revealed that the 2-bromo- and 2-chloro-β-D-xylo-hexopyranosid-3-uloses readily equilibrated with their hydrates, but the remaini
REACTIONS OF METHYL 4,6-O-BENZYLIDENE-2,3-DIDEOXY-2-C-p-TOLYLSULFONYL-α-D-erythro-HEX-2-ENOPYRANOSIDE AND ITS PHENYL ANALOGUE WITH SODIUM METHOXIDE
Sakakibara, Tohru,Yamamoto, Azuma,Ishido, Yoshiharu
, p. 77 - 86 (2007/10/02)
Reaction of the title methyl glycoside 5 with methanolic sodium methoxide afforded mainly the isomeric α-D-erythro-hex-3-enopyranoside derivative 13, formed by migration of the double bond from C-2 to C-3, together with 1,5-anhydro-4,6-O-benzylidene-2-deo
