68907-47-1

Upstream product

• 95058-48-3 (1aR,2S,6R,7bR)-2-Methoxy-1a-methyl-6-phenyl-hexahydro-1,3,5,7-tetraoxa-cyclopropa[a]naphthalene 
• 108-24-7 acetic anhydride 
• 2880-96-8 methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside 
• 917-54-4 methyllithium 

Downstream Products

• 121388-97-4 3,4-di-O-acetyl-1,5-anhydro-6-O-benzyl-2-deoxy-2-C-methyl-D-altritol 
• 121388-96-3 methyl 3,4-di-O-acetyl-6-O-benzyl-2-deoxy-2-C-methyl-α-D-altropyranoside 
• 109958-35-2 (2R,4aR,6S,7S,8S,8aS)-8-Benzyloxy-6-methoxy-7-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 121467-58-1 (2R,4aR,6S,7S,8aR)-6-Methoxy-7-methyl-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one 
• 75837-45-5 methyl 3-O-benzyl-2-deoxy-2-C-methyl-α-D-altropyranoside 
• 64526-80-3 methyl 4,6-O-benzylidene-2-deoxy-2-C-methyl-α-D-arabino-hexopyranosid-3-ulose 
• 68907-48-2 methyl 4,6-O-benzylidene-2-deoxy-2-C-methyl-3-O<(thiomethyl)-thiocarbonyl>-α-D-altro-pyranoside 
• 457623-06-2 1-((2S,6S)-6-Methoxy-5-methyl-3,6-dihydro-2H-pyran-2-yl)-ethanone 
• 220094-47-3 (2R,3S,4S,5R,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-6-methoxy-5-methyl-tetrahydro-pyran-3,4-diol 
• 220094-49-5 tert-Butyl-((1S,2R,4S,5R,6S)-4-methoxy-5-methyl-3,7-dioxa-bicyclo[4.1.0]hept-2-ylmethoxy)-diphenyl-silane 
• 87318-99-8 (2S,3R,4R,5R,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-6-methoxy-3,5-dimethyl-tetrahydro-pyran-4-ol 
• 189453-10-9 epothilone D 
• 152044-54-7 epothilone B 

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