163041-06-3

Upstream product

• 163181-10-0 2-{(2S,3S,4S,5S,6S)-4-Benzyloxy-6-benzyloxymethyl-5-[(4S,5R,6R)-5,7-bis-benzyloxy-6-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-2-oxo-heptyl]-2-[10-(4-methoxy-benzyloxy)-decyl]-tetrahydro-pyran-3-yl}-isoindole-1,3-dione 
• 163040-79-7 2-[(2S,3S,4S,5S,6S)-4-Benzyloxy-6-benzyloxymethyl-2-[10-(4-methoxy-benzyloxy)-decyl]-5-(2-oxo-propyl)-tetrahydro-pyran-3-yl]-isoindole-1,3-dione 
• 1027603-80-0 Acetic acid (2S,3R,4S,5S,6S)-6-acetoxymethyl-4-benzyloxy-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-5-(2-methyl-allyl)-tetrahydro-pyran-2-yl ester 
• 163040-78-6 2-[(2S,3S,4S,5S,6S)-2-Allyl-4-benzyloxy-6-benzyloxymethyl-5-(2-methyl-allyl)-tetrahydro-pyran-3-yl]-isoindole-1,3-dione 
• 163040-77-5 Acetic acid (2S,3S,4S,5S,6S)-6-allyl-4-benzyloxy-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(2-methyl-allyl)-tetrahydro-pyran-2-ylmethyl ester 
• 163041-02-9 2-[(2S,3S,4S,5S,6S)-2-Allyl-4-benzyloxy-6-hydroxymethyl-5-(2-methyl-allyl)-tetrahydro-pyran-3-yl]-isoindole-1,3-dione 
• 163040-76-4 2-[(1S,2S,3S,4R,5R)-3-Benzyloxy-2-(2-methyl-allyl)-6,8-dioxa-bicyclo[3.2.1]oct-4-yl]-isoindole-1,3-dione 
• 163041-01-8 (1S,2S,3S,4R,5R)-4-Azido-3-benzyloxy-2-(2-methyl-allyl)-6,8-dioxa-bicyclo[3.2.1]octane 
• 163041-09-6 (2S,3R)-2,4-bis(benzyloxy)-3-(tert-butyldimethylsilanyloxy)butyraldehyde 
• 138061-50-4 1,3-O-Dibenzyl-2-O-(tert-butyldimethylsilyl)threitol 
• 110104-41-1 (1S,2S,3S,4R,5R)-2-(2-Methyl-2-propenyl)-4-(p-toluenesulfonyl)oxy-6,8-dioxabicyclo<3.2.1>octan-3-ol 
• 131522-45-7 (1S,2S,3S,4S,5R)-2-(2-Methyl-2-propenyl)-3,4-epoxy-6,8-dioxabicyclo<3.2.1>octan-3-ol 
• 6167-32-4 1,6:3,4-dianhydro-2-O-tosyl-D-galactose 

Downstream Products

• 163040-87-7 2-{(2S,3S,4S,5S,6S)-4-Benzyloxy-5-((2S,5S,6R)-5-benzyloxy-6-benzyloxymethyl-4-oxo-tetrahydro-pyran-2-ylmethyl)-6-benzyloxymethyl-2-[10-(4-methoxy-benzyloxy)-decyl]-tetrahydro-pyran-3-yl}-isoindole-1,3-dione 

Relevant academic research and scientific papers

Preferred conformation of C-glycosides. 14. Synthesis and conformational analysis of carbon analogs of the blood groupp determinant H-type II

The syntheses of C-trisaccharides 1-4, carbon analogs of the human blood group determinant H-type II, have been achieved in a flexible and efficient manner. Vicinal coupling constants in the 1H NMR spectrum provide experimental evidence that ea