79646-64-3

Upstream product

• 79607-39-9 (2S,6S)-2-Methoxy-5-methyl-3-methylene-6-trityloxymethyl-3,6-dihydro-2H-pyran 
• 73656-98-1 (2S,5S,6S)-2-Methoxy-5-methyl-3-methylene-6-trityloxymethyl-tetrahydro-pyran 
• 68880-94-4 methyl 2,3,4-trideoxy-2-C-methyl-6-O-triphenylmethyl-α-D-threo-hexopyranoside 
• 68880-93-3 methyl 2,3-dideoxy-2-C-methyl-6-O-triphenylmethyl-α-D-threo-hexopyranosid-4-ulose 
• 76-83-5 trityl chloride 
• 68880-91-1 methyl 2,3-dideoxy-2-C-methyl-α-D-arabino-hexopyranoside 
• 68880-92-2 methyl 2,3-dideoxy-2-C-methyl-6-O-(triphenylmethyl)-α-D-arabino-hexopyranoside 
• 68907-48-2 methyl 4,6-O-benzylidene-2-deoxy-2-C-methyl-3-O<(thiomethyl)-thiocarbonyl>-α-D-altro-pyranoside 
• 68880-90-0 methyl 4,6-O-benzylidene-2,3-dideoxy-2-C-methyl-α-D-arabino-hexopyranoside 
• 79607-37-7 methyl 3,4-dideoxy-4-c-methyl-6-o-trityl-α-D-glycero-hex-3-enopyranosid-2-ulose 
• 79607-38-8 (2S,5S,6S)-2-Methoxy-5-methyl-6-trityloxymethyl-dihydro-pyran-3-one 

Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS OF(-)-α-MULTISTRIATIN FROM D-GLUCOSE

D-glucose was converted into (-)-α-multistriatin, the aggregation pheromone of the Europian elm bark beetle, via a highly stereoselective eighteen-step route

A ROUTE TO PRELOG-DJERASSI LACTONE FROM METHYL α,D-GLUCOPYRANOSIDE

The enone 1 obtainable from methyl α,D-glucopyranoside is converted into the corresponding diene 5 which is hydrogenated to give predominantly the diequatorial dimethyl hexopyranoside 3.C6 of the latter is converted stepwise to the methyl ketone from whic