90661-40-8Relevant academic research and scientific papers
Total syntheses of d-allo-1-deoxynojirimycin and l-talo-1-deoxynojirimycin via reductive cyclization
Chavan, Subhash P.,Dumare, Nilesh B.,Pawar, Kailash P.
, p. 40852 - 40858 (2015/02/05)
Synthesis of a polyhydroxypiperidine framework for l-talo-1-deoxynojirimycin and d-allo-1-deoxynojirimycin was achieved from l-tartaric acid by employing flash dihydroxylation and reductive lactamisation as the key steps. This journal is
De novo asymmetric syntheses of D- and L-talose via an iterative dihydroxylation of dienoates
Ahmed, Md. Moinuddin,O'Doherty, George A.
, p. 10576 - 10578 (2007/10/03)
A short and highly efficient route to D- and L-tafo-γ-lactones has been developed. The key transformation was the sequential osmium-catalyzed bis-dihydroxylation reaction of substituted 2,4-dienoates. When the first dihydroxylation reaction is performed o
4-O-Benzyl-23-O-isopropylidene-L-threose: A useful building block for stereoselective synthesis of monosaccharides
Mukaiyama, Teruaki,Suzuki, Keisuke,Yamada, Tohru,Tabusa, Fujio
, p. 265 - 276 (2007/10/02)
4-O-Benzyl-23-O-isopropylidene-L-threose readily available from L-tartaric acid is a quite useful four-carbon building block for monosaccharide synthesis. The versatility can be reinforced by the coupled use of stereoselective addition reactions where the
A FORMAL TOTAL SYNTHESIS OF POLYOXIN J USING 4-O-BENZYL-2,3-O-ISOPROPYLIDENE-L-THREOSE AS A COMMON CHIRAL BUILDING BLOCK
Tabusa, Fujio,Yamada, Tohru,Suzuki, Keisuke,Mukaiyama, Teruaki
, p. 405 - 408 (2007/10/02)
A convergent formal total synthesis of Polyoxin J was achieved.Two fragments, deoxypolyoxin C and 5-O-carbamoylpolyoxamic acid, were synthetized in a highly stereoselective manner from the common chiral building block, 4-O-benzyl-2,3-O-isopropylidene-L-th
