189210-39-7

Upstream product

• 63522-23-6 3-desoxy-1,2-O-isopropylidene-3-C-methylidene-α-D-erythro-pentodialdo-1,4-furanose 
• 100-58-3 phenylmagnesium bromide 

Downstream Products

• 184881-66-1 Toluene-4-sulfonic acid (2R,3R,4R,5R)-2-benzyl-3,4-dihydroxy-5-triisopropylsilanyloxy-tetrahydro-furan-3-ylmethyl ester 
• 184881-62-7 Toluene-4-sulfonic acid (2R,3R,4R,5S)-2-benzyl-3,4-dihydroxy-5-triisopropylsilanyloxy-tetrahydro-furan-3-ylmethyl ester 
• 184881-67-2 (3R,4R,6R,7R)-4-Benzyl-6-triisopropylsilanyloxy-1,5-dioxa-spiro[2.4]heptan-7-ol 
• 184881-63-8 (3R,4R,6S,7R)-4-Benzyl-6-triisopropylsilanyloxy-1,5-dioxa-spiro[2.4]heptan-7-ol 
• 184881-60-5 Toluene-4-sulfonic acid (3aR,5R,6S,6aR)-5-benzyl-6-hydroxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ylmethyl ester 
• 184881-59-2 (3aR,5R,6S,6aR)-5-Benzyl-6-hydroxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 
• 189210-47-7 (3S,4R)-4-Benzyl-6-hydroxy-1,5-dioxa-spiro[2.4]heptan-7-one 
• 184881-57-0 (3aR,5R,6aR)-5-Benzyl-2,2-dimethyl-6-methylene-tetrahydro-furo[2,3-d][1,3]dioxole 

Relevant academic research and scientific papers

Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics

Highly oxidated sidechain moiety of antitumor terpentecin and related antibiotics is prepared in a stereoselective manner from diacetone glucose through furanoside intermediates.