109914-99-0

Upstream product

• 109915-02-8 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-lyxopyranosid-3-ulose 
• 676-58-4 methylmagnesium chloride 
• 118360-84-2 methyl 3,4-anhydro-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside 
• 109914-96-7 methyl 3-O-benzyl-2,4-dideoxy-2-C-methyl-4-C-methylene-6-O-trityl-α-D-arabino-hexopyranoside 
• 118360-81-9 methyl 4-bromo-2,4-dideoxy-2-C-methyl-6-O-triphenylmethyl-α-D-idopyranoside 
• 118360-83-1 methyl 2,3-anhydro-4-bromo-4-deoxy-6-O-trityl-α-D-gulopyranoside 
• 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 
• 109914-91-2 methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside 
• 75837-44-4 methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-C-methyl-α-D-altropyranoside 
• 109915-01-7 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-arabino-hexopyranosid-3-ulose 
• 109915-00-6 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-altropyranoside 

Downstream Products

• 73679-58-0 methyl 2,3,4-trideoxy-2,4-di-C-methyl-6-O-(triphenylmethyl)-α-D-arabino-hexopyranoside 
• 79646-63-2 methyl 2,3,4-trideoxy-2,3-di-C-methyl-6-O-trityl-α-D-ribo-hexopyranoside 
• 109915-02-8 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-lyxopyranosid-3-ulose 
• 109914-99-0 (2S,3R,5S,6S)-2-Methoxy-3,5-dimethyl-6-trityloxymethyl-tetrahydro-pyran-4-ol 
• 118360-86-4 methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-talopyranoside 

Relevant academic research and scientific papers

Stereoselective Syntheses of 1,3,5-Trihydroxy-2,4-dimethylpentane Equivalents from Methyl α-Mannopyranosides

The optically active 1,3,5-trihydroxy-2,4-dimethylpentane equivalents: methyl 2,4-dideoxy-2,4-di-C-methyl-α-D-ido- and talopyranosides and their enantiomers, which should be suitable for the syntheses of propionate-derived natural products, were stereo- a

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