195192-35-9

Upstream product

• 32934-24-0 S-ethyl 2,3,4,6-tetra-O-acetyl-1-deoxy-1-thio-α-D-mannopyranoside 
• 195192-33-7 ethyl 2,3-O-isopropylidene-1-thio-6-O-triphenylmethyl-α-D-mannopyranoside 
• 128850-48-6 ethyl 1-thio-6-O-triphenylmethyl-α-D-mannopyranoside 
• 316188-11-1 ethyl 6-O-[(tert-butyl)diphenylsilyl]-1-thio-α-D-mannopyranoside 
• 316188-13-3 ethyl 6-O-[(tert-butyl)diphenylsilyl]-2,3-di-O-isopropylidene-1-thio-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 7473-36-1 ethyl 1-thio-α-D-mannopyranoside 
• 195192-34-8 ethyl 4-O-benzyl-2,3-O-isopropylidene-1-thio-6-O-trityl-α-D-mannopyranoside 

Downstream Products

• 195192-37-1 (R)-1-((3aS,4R,6R,7S,7aS)-7-Benzyloxy-4-ethylsulfanyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-2-(dimethyl-phenyl-silanyl)-ethanol 
• 195192-39-3 (2R,3S,4R,5S,6S)-5-Benzyloxy-6-[(R)-1-benzyloxy-2-(dimethyl-phenyl-silanyl)-ethyl]-2-ethylsulfanyl-tetrahydro-pyran-3,4-diol 
• 195192-38-2 [(R)-2-Benzyloxy-2-((3aS,4R,6S,7S,7aS)-7-benzyloxy-4-ethylsulfanyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-ethyl]-dimethyl-phenyl-silane 
• 195192-40-6 (2R,3S,4R,5S,6S)-4,5-Bis-benzyloxy-6-[(R)-1-benzyloxy-2-(dimethyl-phenyl-silanyl)-ethyl]-2-ethylsulfanyl-tetrahydro-pyran-3-ol 
• 195192-42-8 Benzoic acid (2R,3S,4S,5S,6S)-4,5-bis-benzyloxy-6-[(R)-1-benzyloxy-2-(dimethyl-phenyl-silanyl)-ethyl]-2-ethylsulfanyl-tetrahydro-pyran-3-yl ester 
• 195192-44-0 Benzoic acid (2S,3S,4S,5S,6S)-4,5-bis-benzyloxy-6-[(R)-1-benzyloxy-2-(dimethyl-phenyl-silanyl)-ethyl]-2-[(2R,3R,4S,5S,6S)-3,5-bis-benzyloxy-2-((R)-1,2-bis-benzyloxy-ethyl)-6-methoxy-tetrahydro-pyran-4-yloxy]-tetrahydro-pyran-3-yl ester 
• 1240564-06-0 ethyl 4,7-di-O-benzyl-2,3-O-isopropylidene-1-thio-D-glycero-α-D-manno-heptopyranoside 

Relevant academic research and scientific papers

1,2-Diacetals in synthesis: Total synthesis of a glycosylphosphatidylinositol anchor of Trypanosoma brucei

A full account on a total synthesis of GPI anchor 1 employing butanediacetal (BDA) groups and a chiral bis(dihydropyran) is presented. The reactivity of selenium and thio glycosides was tuned by the use of BDA groups. This allowed the assembly of an appro

Synthesis of a trisaccharide fragment corresponding to the lipopolysaccharide region of vibrio parahaemolyticus

Vicinal syn-dihydroxylation of D-manno-hept-6-enopyranosides 4 and 10 with OsO4 afforded D-glycero-α-D-manno-heptopyranosides 5 and 11, respectively, in good yield and with a high degree of stereoselectivity. Compound 5 was converted into DD-He