75879-82-2

Upstream product

• 108-24-7 acetic anhydride 
• 2880-96-8 methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside 
• 75837-51-3 methyl (2R)-4,6-O-benzylidene-2-methyl-2-deoxy-α-D-threo-hex-3-ulopyranoside 
• 4288-93-1 methyl 4,6-O-benzylidene-α-D-galactopyranoside 
• 95058-48-3 (1aR,2S,6R,7bR)-2-Methoxy-1a-methyl-6-phenyl-hexahydro-1,3,5,7-tetraoxa-cyclopropa[a]naphthalene 
• 3257-59-8 methyl 2,3-anhydro-4,6-O-benzylidene-α-D-gulopyranoside 
• 917-54-4 methyllithium 

Downstream Products

• 84207-40-9 Benzoic acid (2R,3R,4S,5S,6S)-3-hydroxy-2-hydroxymethyl-6-methoxy-5-methyl-tetrahydro-pyran-4-yl ester 
• 84207-41-0 methyl 3-O-benzoyl-6-O-(tert-butyldimethylsilyl)-2-C-methyl-α-D-idopyranoside 
• 84207-42-1 methyl 3-O-benzoyl-6-O-(tert-butyldimethylsilyl)-2-deoxy-4-O-toluene-p-sulfonyl-α-D-idopyranoside 
• 93403-85-1 methyl (2R)-4,6-O-benzylidene-2-methyl-2-((methylthio)methyl)-2-deoxy-α-D-threo-hex-3-ulopyranoside 
• 93403-86-2 (4aR,6S,8aR)-6-Methoxy-7,7-dimethyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-ol 
• 75837-51-3 methyl (2R)-4,6-O-benzylidene-2-methyl-2-deoxy-α-D-threo-hex-3-ulopyranoside 
• 84207-39-6 methyl 3-O-benzoyl-4,6-O-benzylidene-2-deoxy-2-C-methyl-α-D-idopyranoside 
• 93403-87-3 C₁₇H₁₇⁽²⁾H₅O₅S 
• 109914-97-8 methyl 3-O-benzyl-2-deoxy-6-O-(diphenyl-t-butylsilyl)-2-C-methyl-4-C-(trimethylsilylmethyl)-α-D-idopyranoside 
• 109914-98-9 methyl 3-O-benzyl-2-deoxy-6-O-(diphenyl-t-butylsilyl)-2-C-methyl-4-C-(trimethylsilylmethyl)-α-D-altro-pyranoside 
• 109914-90-1 methyl 3-O-benzyl-2-deoxy-6-O-(diphenyl-t-butylsilyl)-2-C-methyl-α-D-altropyranoside 
• 109914-94-5 O-(diphenyl-t-butylsilyl)-2-C-methyl-α-D-idopyranoside 
• 109915-01-7 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-arabino-hexopyranosid-3-ulose 
• 109915-02-8 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-lyxopyranosid-3-ulose 

Relevant academic research and scientific papers

An Approach to the Total Synthesis of the Prelog-Djerassi Lactone

An approach to the synthesis of the Prelog-Djerassi lactone using D-glucose as a starting material is described.The use of Swern oxidation provides an efficient means of preparing carbohydrate ketones.An unusual departure from the normal reaction pathway

Chiral Synthons for the Total Synthesis of Macrolide Antibiotics

All the methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-dimethyl-t-butylsilyl-α-D-hexopyranosides, chiral intermediates in the total synthesis of many biologically important natural products have been prepared.