73679-58-0

Upstream product

• 68880-93-3 (2R,5R,6S)-6-Methoxy-5-methyl-2-trityloxymethyl-dihydro-pyran-3-one 
• 68880-92-2 (2R,3S,5R,6S)-6-Methoxy-5-methyl-2-trityloxymethyl-tetrahydro-pyran-3-ol 
• 101978-79-4 Methyl 4,6-O-benzylidene-2-deoxy-2-C-methyl-α-D-allopyranoside 
• 105930-42-5 (2R,4aR,6S,7R,8aS)-6-Methoxy-7-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 66149-56-2 methyl 3,4-dideoxy-4-C-methyl-6-O-(triphenylmethyl)-α-D-threo-hexopyranosid-2-ulose 
• 35303-94-7 (2S,6S)-2-Methoxy-6-trityloxymethyl-6H-pyran-3-one 
• 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 
• 109915-00-6 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-altropyranoside 
• 109914-99-0 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-idopyranoside 
• 19465-06-6 methyl 4,6-O-benzylidene-2-deoxy-2-C-methyl-α-D-altropyranoside 
• 2880-96-8 methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside 
• 75837-45-5 methyl 3-O-benzyl-2-deoxy-2-C-methyl-α-D-altropyranoside 
• 109914-92-3 methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-arabino-hexapyranosid-4-ulose 

Downstream Products

• 105897-94-7 Toluene-4-sulfonic acid (1S,2R,4R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-4-[1,3]dithian-2-yl-2-methyl-pentyl ester 

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

STEREOSELECTIVE TOTAL SYNTHESIS AND STEREOCHEMISTRY OF DIPLODIATOXIN, A MYCOTOXIN FROM DIPLODIA MAYDIS

The stereochemistry of diplodiatoxin has been deduced, and the assumed stereostructure has been confirmed by the synthesis using highly stereocontrolled strategy, in which the intramolecular Diels-Alder reaction of a(E, E, E)-triene is involved.

Synthetic Routes to 6,8-Dioxabicyclooctyl Pheromones from D-Glucose Derivatives. 4. Synthesis of (-)-α-Multistriatin

The precursor for (-)-α-multistriatin (alkyl 2,3,4-trideoxy-2,4-di-C-methyl-α-D-lyxo-hexopyranoside) may be approached from the corresponding isomeric 4-oxo-2-C-methyl- or 2-oxo-4-C-methylpyranosides by (a) methylenation followed by (b) hydrogenation.The