137101-01-0Relevant articles and documents
De novo highly stereocontrolled synthesis of 2,6-dideoxy sugars by use of 2,6-anhydro-2-thio sugars
Toshima, Kazunobu,Yoshida, Takehito,Mukaiyama, Satsuki,Tatsuta, Kuniaki
, p. 173 - 188 (2007/10/02)
Representative 2,6-dideoxy sugars, L-cladinose (1), L-(mycarose (2), L-oleandrose (3), L-olivose (4), and all of their C-3 epimers, 2,6-dideoxy-3-C-methyl-3-O-methyl-L-arabino-hexopyranose (26), 2,6-dideoxy-3-C-methyl-L-arabino-hexopyranose (L-olivomycose
De Novo highly stereocontrolled synthesis of 2,6-dideoxy-C-3-branched carbohydrates by use of 2,6-anhydro-2-thio sugar:L-cladinose and its C-3 epimer
Toshima, Kazunobu,Yoshida, Takehito,Mukaiyama, Satsuki,Tatsuta, Kuniaki
, p. 4139 - 4142 (2007/10/02)
L-Cladinose (1) and its C-3 epimer 2 were synthesized through a highly stereo selective addition of methyl anion to the C-3 carbonyl groups of α-anomer 9 and β-anomer 10 having 2,6-anhydro-2-thio structures, respectively, which were prepared from the comm
