Stereospecific Synthesis and NMR Conformational Studies of .gamma.-Butyrolactones of Nucleosides as Chiral Synthons for the Preparation of 2'-C- and 3'-C-Branched-Chain Nucleosides

1994 ◽  
Vol 59 (25) ◽  
pp. 7661-7670 ◽  
Author(s):  
Sonsoles Velazquez ◽  
Maria Luisa Jimeno ◽  
Sophie Huss ◽  
Jan Balzarini ◽  
Maria-Jose Camarasa
Keyword(s):  
Stereospecific Synthesis ◽  
Conformational Studies ◽  
Branched Chain

Oxidation of a branched-chain alditol by Acetobacter suboxydans: A stereospecific synthesis of l-dendroketose

1977 ◽  
Vol 53 (1) ◽  
pp. 101-108 ◽  
Author(s):  
Walter A. Szarek ◽  
G.Wayne Schnarr ◽  
Harold C. Jarrell ◽  
J.K.N. Jones
Keyword(s):  
Stereospecific Synthesis ◽  
Acetobacter Suboxydans ◽  
Branched Chain

A new approach to the stereospecific synthesis of branched-chain sugars

1988 ◽  
pp. 1581 ◽  
Author(s):  
Ton That Thang ◽  
Maria de los A. Laborde ◽  
Alain Olesker ◽  
Gabor Lukacs
Keyword(s):  
Stereospecific Synthesis ◽  
New Approach ◽  
Branched Chain

ChemInform Abstract: A New Approach to the Stereospecific Synthesis of Branched-Chain Sugars.

ChemInform ◽  
1989 ◽  
Vol 20 (27) ◽  
Author(s):  
T. T. THANG ◽  
M. A. LABORDE ◽  
A. OLESKER ◽  
G. LUKACS
Keyword(s):  
Stereospecific Synthesis ◽  
New Approach ◽  
Branched Chain

Branched-chain sugars. Reaction of furanoses with formaldehyde: a stereospecific synthesis of L-dendroketose

1979 ◽  
Vol 57 (4) ◽  
pp. 384-386 ◽  
Author(s):  
Pak-Tsun Ho
Keyword(s):  
Stereospecific Synthesis ◽  
Branched Chain ◽  
Simple Conversion

A simple conversion of 2,3-O-isopropylidene-D-hamamelose, prepared by reaction of 2,3-O-isopropylidene-D-ribose with formaldehyde, into L-dendroketose is described.

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