106445-05-0Relevant academic research and scientific papers
Highly stereoselective indium trichloride-catalysed asymmetric aldol reaction of formaldehyde and a glucose-derived silyl enol ether in water
Loh, Teck-Peng,Chua, Guan-Leong,Vittal, Jagadese J.,Wong, Meng-Wah
, p. 861 - 862 (2007/10/03)
The yield and stereochemical outcome of the reaction between D-glucose-derived silyl enol ether 1 (Z and E isomers) and commercial formaldehyde in water catalysed by indium(III) choride was studied.
Zaragozic acid a : Interesting observations in anhydro-ring formation of densely functionalised carbohydrate templates
Gurjar, Mukund K.,Das, Sanjoy K.,Saha, Uttam K.
, p. 2241 - 2244 (2007/10/02)
A methodology which produced highly substituted 1,6-anhydrofuranose derivative, symbolising 2,8-dioxobicyclo[3.2.1]octan core of zaragozic acid, has been described.
A formal synthesis of a novel immunosuppressant ISP-1 : Stereocontrolled Pd(O) catalysedcis-hydroxyamination of carbohydrate derived vinyl epoxide
Rao, A. V. Rama,Gurjar, Mukund K.,Devi, T. Rama,Kumar, K. Ravi
, p. 1653 - 1656 (2007/10/02)
Described herein are the results leading to the synthesis of ISP-1 containing an unusal α, α-disubstituted amino acid and whose immunosuppressive activity only has recently been discovered.
SYNTHESES OF PSEUDO-α-D-GLUCOPYRANOSE AND PSEUDO-β-L-IDOPYRANOSE, TWO OPTICALLY ACTIVE PSEUDO-HEXOPYRANOSES, FROM D-GLUCOSE BY USING STEREOSELECTIVE REDUCTIVE DEACETOXYLATION WITH SODIUM BOROHYDRIDE AND CYCLITOL FORMATION FROM NITROFURANOSE AS KEY REACTIO
Yoshikawa, Masayuki,Cha, Bae Cheon,Nakae, Takahiko,Kitagawa, Isao
, p. 3714 - 3717 (2007/10/02)
Two optically active pseudo-hexopyranoses, pseudo-α-D-glucopyranose and pseudo-β-L-idopyranose, have been synthesized from D-glucose by using stereoselective deacetoxylations with NaBH4 and cyclitol formations from nitrofuranose derivatives as key reactio
1,3,5-TRIDEOXY-3,5-DI-C-METHYL-L-TALITOL: A CHIRON FOR THE C-33-C-37 SEGMENT OF AMPHOTERICIN B
Liang, David,Schuda, Ann DeCamp,Fraser-Reid, Bert
, p. 229 - 240 (2007/10/02)
1,3,5-Trideoxy-3,5-di-C-methyl-L-talitol is a potential chiron for the C-33-C-37 segment of amphotericin B.This hexitol has been synthesized from 3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose by a route in which a C-methylene derivative at C-5 is hydr
