492470-88-9

Upstream product

• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 205485-61-6 2-((3S,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-ylsulfanyl)-pyridine 
• 492470-84-5 1-((2R,3S,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-((2R,3R,4S,5S)-3,4-bis-benzyloxy-5-methoxy-tetrahydro-furan-2-yl)-2-nitro-ethanol 
• 492470-87-8 C₃₄H₃₂O₇ 
• 492470-85-6 (2S,3S,4R,5R)-3,4-Bis-benzyloxy-2-methoxy-5-nitromethyl-tetrahydro-furan 
• 492470-86-7 (2S,3S,4S,5S)-3,4-Bis-benzyloxy-2-iodomethyl-5-methoxy-tetrahydro-furan 
• 222555-96-6 2,5-anhydro-3,4-di-O-benzyl-D-mannitol 
• 86363-73-7 (2R,3S,4S,5R)-3,4-dihydroxy(tetrahydrofuran-2,5-diyl)bis(methylene) dibenzoate 
• 102208-55-9 2,5-anhydro-3,4,6-tri-O-benzyl-D-mannitol 
• 100-39-0 benzyl bromide 
• 16896-03-0 methyl 2,3-di-O-benzyl-α-D-arabinofuranoside 
• 94273-27-5 2,5-anhydro-3,4,6-tris-O-(phenylmethyl)-D-mannose 
• 697298-48-9 methyl 2,3-di-O-benzyl-5-dehydro-α-D-arabinofuranoside 
• 853260-29-4 (2R,3R,4S,5S)-3,4-Bis-benzyloxy-2-(2,2-dibromo-vinyl)-5-methoxy-tetrahydro-furan 

Relevant academic research and scientific papers

Samarium diiodide mediated coupling of 2-pyridylsulfonyl furanosides with aldehydes and ketones: A general synthesis of C-furanosides

Diiodosamarium-mediated coupling of anomeric 2-pyridyl sulfones derived from furanosides with carbonyl compounds, aldehydes, and ketones gave α-hydroxylated 2,5-trans-dialkylated tetrahydrofurans with good yields and useful stereoselectivities. The main c

Synthesis of C-disaccharide analogues of the α-D-arabinofuranosyl- (1→5)-α-D-arabinofuranosyl motif of mycobacterial cell walls via alkynyl intermediates

Two C-glycosides related to the recurrent α-D-arabinofuranosyl- (1→5)-α-D-arabinofuranosyl structural motif of mycobacterial arabinan have been prepared by routes involving acetylenic intermediates.

First synthesis of methyl α-C-D-arabinofuranosyl-(1→5)-α-D-arabinofuranoside: The C-disaccharide segment of motif C of Mycobacterium tuberculosis

The synthesis of C-analogue of the disaccharide 2 α-araf-(1→5)-araf, present in motif C of the arabino-galactan portion of Mycobacterium tuberculosis, has been described. The critical C-C bond formation reaction to couple both the furanosyl residues has b