106974-28-1

Upstream product

• 122-04-3 4-nitro-benzoyl chloride 
• 106929-12-8 (2R,3R,4R,5R)-4,5-Bis-benzyloxy-1-((1S,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-(4-methoxy-benzyloxy)-pentan-2-ol 
• 2746-25-0 p-Methoxybenzyl bromide 
• 106929-11-7 (2R,3R,4R,5R)-4,5-Bis-benzyloxy-1-((1S,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pentane-2,3-diol 
• 106929-16-2 4-Nitro-benzoic acid (2S,3S,4R,5R,6R)-3,4-bis-benzyloxy-6-((1S,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-ylmethyl)-5-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yl ester 

Downstream Products

• 106929-17-3 (2R,3R,4R,5R)-4,5-Bis-benzyloxy-2-((1S,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-ylmethyl)-6-propa-1,2-dienyl-tetrahydro-pyran-3-ol 
• 106929-14-0 Benzoic acid (2R,3R,4R,5S,6R)-3,4-bis-benzyloxy-6-((1S,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-ylmethyl)-5-hydroxy-tetrahydro-pyran-2-ylmethyl ester 
• 106929-14-0 Benzoic acid (2R,3R,4R,5R,6R)-3,4-bis-benzyloxy-6-((1S,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-ylmethyl)-5-hydroxy-tetrahydro-pyran-2-ylmethyl ester 
• 106929-18-4 (2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-2-((1S,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-ylmethyl)-6-hydroxymethyl-tetrahydro-pyran-3-ol 
• 106974-30-5 Benzoic acid (2R,3R,4R,6R)-3,4-bis-benzyloxy-6-((1S,2R,3S,4R,5R)-3,4-bis-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-2-ylmethyl)-5-hydroxy-tetrahydro-pyran-2-ylmethyl ester 

Relevant academic research and scientific papers

Preferred Conformation of C-Glycosides. 8. Synthesis of 1,4-Linked Carbon Disaccharides

Three general synthetic routes to 1,4-linked carbon disaccharides (e.g., 3, 4, 15-17, 21-23, 44, and 45) are presented.Control of the stereochemistry at C.1', C.2', C.5'and C.4, the incorporation of deuterium labels at the C.α position, and structural mod

Synthesis of C-Disaccharides

Stereocontrolled syntheses of four C-disaccharides 10, 11, 16, and 17 were reported.The (n-Pr)3SiH/BF3*Et2O reduction of hemiketals such as 7 yielded the equatorially substituted C-glycoside as the major product while C-alkylation (CHCCH2Si(CH3)3/BF3*E