167904-07-6

Basic information

• Product Name: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone
• Synonyms: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone
• CAS NO: 167904-07-6
• Molecular Weight: 538.64
• Mol File: 167904-07-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone(167904-07-6)
• EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-L-altrono-1,5-lactone(167904-07-6)

Safety Data

• Hazardous Substances Data: 167904-07-6(Hazardous Substances Data)

Upstream product

• 167904-03-2 2,3,4,6-tetra-O-benzyl-D-galactononitrile 
• 168037-62-5 (Z)-2,3,4,6-tetra-O-benzyl-D-galactose oxime 
• 270062-22-1 1N-benzyloxy-2,3,4,6-tetrakis(benzyloxy)-5-hydroxy-(2R,3S,4S,5R)-hexanamide 
• 82598-84-3 2,3,4,6-tetra-O-benzyl-D-galactonolactone 
• 60656-87-3 benzyloxyacetoaldehyde 
• 905732-75-4 (2R,3R,4S,5S)-4,6-Bis-benzyloxy-2,3,5-trihydroxy-hexanoic acid methyl ester 
• 905732-74-3 (E)-(4R,5S)-4,6-Bis-benzyloxy-5-hydroxy-hex-2-enoic acid methyl ester 
• 905732-76-5 (3R,4R,5R,6S)-5-Benzyloxy-6-benzyloxymethyl-3,4-dihydroxy-tetrahydro-pyran-2-one 
• 100-39-0 benzyl bromide 
• 270062-27-6 2N-benzyloxy-3,4,5-tris(benzyloxy)-6-benzyloxymethyl-(3R,4S,5S,6S)-tetrahydro-2H-pyran-2-imine 
• 167904-05-4 2,3,4,6-tetra-O-benzyl-L-altrononitrile 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

Direct one-pot highly enantioselective assembly of polyketide and carbohydrate synthons

A short, direct, catalytic, enantioselective synthesis of polyketide segments and carbohydrates is presented. The novel, direct, one-pot, organocatalytic asymmetric tandem cross-aldol/Horner-Wittig-Emmons reactions assemble polyketide and carbohydrate der

Intramolecular Tishchenko reactions of protected hexos-5-uloses: A novel and efficient synthesis of L-idose and L-altrose

Protected t-butyl esters of aldonic acids with the rare L-ido and L- altro configuration can be effectively obtained by a diastereoselective Tishchenko reaction of hexos-5-uloses induced by t-BuOSmI2. These compounds can be easily converted int