105368-79-4Relevant academic research and scientific papers
A Novel Transformation of Four Aldoses to Some Optically Pure Pseudohexopyranoses and a Pseudopentofuranose, Carboxylic Analogues of Hexopyranoses and Pentofuranose. Synthesis of Derivatives of (1S,2S,3R,4S,5S)-, (1S,2S,3R,4R,5S)-, (1R,2R,3R,4R,5S)-, (1S,
Tadano, Kin-ichi,Maeda, Hiroo,Hoshino, Masahide,Iimura, Youichi,Suami, Tetsuo
, p. 1946 - 1956 (2007/10/02)
Knoevenagel reactions with dimethyl malonate of the suitably protected acylic aldehydes 6, 20, 34, and 46, which were prepared from D-ribose, D-xylose, D-arabinose, and D-erythrose, respectively, proceeded smoothly to provide α,β-unsaturated diesters 7, 2
A NEW TRANSFORMATION OF ALDOSE DERIVED SYNTHONS TO PSEUDO-HEXOPYRANOSE OR PSEUDO-PENTOFURANOSE DERIVATIVES
Tadano, Kin-ichi,Maeda, Hiroo,Hoshino, Masahide,Iimura, Youichi,Suami, Tetsuo
, p. 1081 - 1084 (2007/10/02)
The D-ribose or D-erythrose derived acyclic synthon, which possesses a 2-malonyl carbon chain at C-1 position, was cyclized stereoselectively to a six- or five-membered carbocycle.Those carbocycles were converted into pseudo-β-L-mannopyranose derivatives
SYNTHESIS OF OPTICALLY ACTIVE PSEUDO-α-D-GLUCOSE AND PSEUDO-β-L-ALTROSE
Suami, Tetsuo,Tadano, Kin-ichi,Kameda, Yukiaki,Iimura, Youichi
, p. 1919 - 1922 (2007/10/02)
Optically active two pseudo-sugars, pseudo-α-D-glucose and pseudo-β-L-altrose have been synthesized by cyclization of 2,3,4-tri-O-benzyl-5-deoxy-5-iodo-L-arabinose with dimethyl malonate in the presence of sodium hydride as a key reaction.
