76404-33-6

Upstream product

• 76739-66-7 3,4-di-O-acetyl-D-rhamnal 
• 100-51-6 benzyl alcohol 
• 755033-94-4 (2S,3R)-3,6-dihydro-2-methyl-6-(phenylmethoxy)-3-O-acetyl-2H-pyran-3-ol 
• 76404-31-4 Benzyl-4-O-methylsulfonyl-2,3-6-tridesoxy-α-L-erythro-hex-2-enopyranosid 
• 34819-86-8 3,4-di-O-acetyl-6-deoxy-L-glucal 
• 76404-29-0 phenylmethyl 4-O-acetyl-2,3,6-trideoxy-α-L-erythro-hex-2-enopyranoside 
• 155016-85-6 Benzyl 2,3,6-trideoxy-4-O-p-nitrobenzoyl-α-L-threo-hex-2-enopyranoside 
• 76404-32-5 Benzyl-4-O-benzoyl-2,3,6-tridesoxy-α-L-threo-hex-2-enopyranosid 
• 71978-92-2 benzyl 4-O-acetyl-6-deoxy-2,3-dideoxy-α/β-D-erythro-hex-2-enopyranoside 

Downstream Products

• 132351-74-7 ((2R,3S)-6-Benzyloxy-2-methyl-3,6-dihydro-2H-pyran-3-yloxy)-tert-butyl-dimethyl-silane 
• 174151-43-0 benzyl 2,3,6-trideoxy-4-O-trichloroacetimidoyl-α-L-threo-hex-2-enopyranoside 
• 76404-37-0 Benzyl-2-O-acetyl-4-O-(4-O-acetyl-2,3,6-tridesoxy-α-L-erythro-hex-2-enopyranosyl)-3,6-didesoxy-3-iod-α-L-idopyranosid 
• 76404-38-1 Benzyl-2-O-acetyl-4-O-(4-O-acetyl-2,3,6-tridesoxy-α-L-erythro-hexopyranosyl)-3,6-didesoxy-α-L-lyxo-hexopyranosid 
• 76404-36-9 Benzyl-2,3-anhydro-4-O-(4-O-acetyl-2,3,6-tridesoxy-α-L-erythro-hex-2-enopyranosyl)-6-desoxy-α-L-talopyranosid 
• 174151-47-4 N-[(2R,3R,4R,5R,6S)-2-Benzyloxy-4-hydroxy-6-methyl-5-(toluene-4-sulfonylamino)-tetrahydro-pyran-3-yl]-acetamide 
• 174151-48-5 N-[(2R,3R,4R,5R,6S)-2-Benzyloxy-5-hydroxy-6-methyl-4-(toluene-4-sulfonylamino)-tetrahydro-pyran-3-yl]-acetamide 
• 174151-44-1 benzyl 2,3,4,6-tetradeoxy-2-trichloroacetamido-α-L-threo-hex-3-enopyranoside 
• 174151-46-3 benzyl 2-acetamido-2,3,4,6-tetradeoxy-α-L-threo-hex-3-enopyranoside 
• 174151-45-2 benzyl 2-amino-2,3,4,6-tetradeoxy-α-L-threo-hex-3-enopyranoside 
• 76404-35-8 Benzyl-2,3-anhydro-6-desoxy-α-L-gulopyranosid 
• 76404-34-7 Benzyl-2,3-anhydro-6-desoxy-α-L-talopyranosid 
• 88818-93-3 benzyl 2,3,4-tri-O-acetyl-6-deoxy-α-L-talopyranoside 

Relevant academic research and scientific papers

Synthesis of the Hexasaccharide Fragment of Landomycin A Using a Mild, Reagent-Controlled Approach

The synthesis of the hexasaccharide fragment of landomycin A is reported. Using p-toluenesulfonyl chloride mediated dehydrative glycosylation, we constructed the deoxy-sugar linkages in a stereoselective fashion without the need for temporary prosthetic g

Reagent Controlled Direct Dehydrative Glycosylation with 2-Deoxy Sugars: Construction of the Saquayamycin Z Pentasaccharide

The first synthesis of the pentasaccharide fragment of the angucycline antibiotic saquayamycin Z is described. By using our sulfonyl chloride mediated reagent controlled dehydrative glycosylation, we are able to assemble the glycosidic linkages with high

SYNTHESIS OF ISOMERIC BENZYL 6-DEOXY-α-L-TALO- AND α-L-GULOPYRANOSIDES

Synthesis of benzyl 2,3,4-tri-O-acetyl-6-deoxy-α-L-talopyranoside (6) and its α-L-gulo isomer 7 was performed by a five-step sequence starting from L-rhamnal 1.The L-talo isomer was proved to be identical with the component of O-antigenic polysaccharide o

A convergent synthesis of optically active aspyrone

Aspyrone (1) was elaborated in an optically pure form by the key reaction involving a nucleophilic addition of δ-lactone enolate to 2-tosyloxyaldehyde and a subsequent in situ formation of epoxide.