76696-17-8

Upstream product

• 13403-13-9 ethyl-β-D-galactofuranoside 
• 59-23-4 D-Galactose 
• 100-44-7 benzyl chloride 
• 76696-16-7 Ethyl-5,6-O-isopropyliden-β-D-galactofuranosid 

Downstream Products

• 88480-98-2 Ethyl-2,3-di-O-benzyl-5,6-di-O-tosyl-β-D-galactofuranosid 
• 88480-97-1 Ethyl-2,3-di-O-benzyl-5-O-tosyl-β-D-galactofuranosid 
• 88480-96-0 Ethyl-5,6-O-di-O-acetyl-2,3-di-O-benzyl-β-D-galactofuranosid 
• 88481-00-9 Ethyl-5-O-acetyl-2,3-di-O-benzyl-6-desoxy-6-iod-β-D-galactofuranosid 
• 88481-03-2 Ethyl-5-O-acetyl-2,3-di-O-benzyl-6-desoxy-β-D-galactofuranosid 
• 88480-99-3 Ethyl-2,3-di-O-benzyl-6-desoxy-6-iod-β-D-galactofuranosid 
• 88481-01-0 Ethyl-5,6-anhydro-2,3-di-O-benzyl-β-D-galactofuranosid 
• 88481-02-1 Ethyl-2,3-di-O-benzyl-β-D-lyxo-hex-5-enofuranosid 
• 76696-19-0 Ethyl-2,3-di-O-benzyl-6-O-tosyl-β-D-galactofuranosid 
• 76696-21-4 Ethyl-2,3-di-O-benzyl-6-desoxy-5-O-methyl-β-D-galactofuranosid 
• 76696-20-3 Ethyl-2,3-di-O-benzyl-6-desoxy-β-D-galactofuranosid 
• 76696-18-9 ethyl 2,3-di-O-benzyl-β-D-galactofuranoside 
• 88480-95-9 Ethyl-6-O-acetyl-2,3-di-O-benzyl-β-D-galactofuranosid 

Relevant academic research and scientific papers

SYNTHESES OF THE CHROMOMYCINONE SIDE CHAIN FROM CARBOHYDRATE PRECURSORS

Appropriate dithiane derivatives of D-threo configuration were prepared starting with D-arabinose and D-galactose, respectively.Their dianions served for nucleophilic additions to model aldehydes, thus comprising syntheses of the complex side chain of chr

Synthesis of the Tetrose Building Unit of the Chromomycinone Side Chain from D-Galactose

Application of the reaction sequence isopropylidenation, benzylation, and acetal cleavage to ethyl-β-D-galactofuranoside (1) leads to the diol 4.The fucose derivative 15 is prepared from 4 by different routes and further transformed into its methyl ether