75721-93-6

Upstream product

• 81644-86-2 2,3,5-tri-O-benzoyl-L-rhamnono-1,4-lactone 
• 73-34-7 L-rhamnose 
• 20031-16-7 L-Rhamnono-1,4-lactone 
• 98-88-4 benzoyl chloride 

Downstream Products

• 865622-63-5 2-Allyl-6-methoxy-benzoic acid (3R,5R)-2-methoxy-5-((S)-1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-furan-3-yl ester 
• 620987-65-7 (1S,3R,4S)-1-(2-cyanoethyl)-3-hydroxy-4-methylhept-6-enyl 6-hydroxy-2-prop-2-enylbenzoate 
• 620987-64-6 1-((1E)-2-cyanovinyl)-(1R,3R,4S)-3-hydroxy-4-methylhept-6-enyl 6-hydroxy-2-prop-2-enylbenzoate 
• 620987-56-6 (3R,5R)-5-((1S)-1-methylbut-3-enyl)-2-hydroxyoxolan-3-yl 6-hydroxy-2-prop-2-enylbenzoate 
• 620987-63-5 (3R,5R)-5-((1S)-1-methylbut-3-enyl)-2-methoxyoxolan-3-yl 6-methoxy-2-prop-2-enylbenzoate 
• 620987-55-5 (3R,5R)-5-((1S)-1-hydroxyethyl)-2-methoxyoxolan-3-yl 6-methoxy-2-prop-2-enylbenzoate 
• 620987-54-4 (3R,5R)-5-((1S)-1-hydroxyethyl)-2-oxo-3,4,5-trihydrofuryl 6-methoxy-2-prop-2-enylbenzoate 

Relevant academic research and scientific papers

Enantiospecific Formal Total Syntheses of (-)-Salicylihalamides A and B from D-Glucose and L-Rhamnose

(Matrix Presented) Two formal chiral pool syntheses of the (-)-salicylihalamides A and B were achieved from commercially available 1,2,5,6-diacetone-D-glucose and L-rhamnose.