128308-28-1

Upstream product

• 128308-27-0 3-[(1S,4S,5R,6S)-5-(tert-Butyl-dimethyl-silanyloxy)-6-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-methoxy-4-methyl-heptyl]-phenol 

Downstream Products

• 128308-09-8 (3S,4R)-6-(2-{(4S,5S,6R)-6-[(1S,4S)-4-(3-Benzyloxy-phenyl)-4-methoxy-1-methyl-butyl]-2,2,5-trimethyl-[1,3]dioxan-4-ylmethyl}-[1,3]dithian-2-yl)-3-(tert-butyl-dimethyl-silanyloxy)-4,6-dimethyl-heptanoic acid methyl ester 
• 128308-17-8 ((2S,3R)-6-{(4S,5S,6R)-6-[(1S,4S)-4-(3-Benzyloxy-phenyl)-4-methoxy-1-methyl-butyl]-2,2,5-trimethyl-[1,3]dioxan-4-ylmethyl}-6-hydroxy-3,5,5-trimethyl-tetrahydro-pyran-2-yl)-acetic acid methyl ester 
• 128308-08-7 (4R,5S,6S)-4-[(1S,4S)-4-(3-Benzyloxy-phenyl)-4-methoxy-1-methyl-butyl]-6-{2-[(3R,4S)-4,6-bis-(tert-butyl-dimethyl-silanyloxy)-1,1,3-trimethyl-hexyl]-[1,3]dithian-2-ylmethyl}-2,2,5-trimethyl-[1,3]dioxane 

Relevant academic research and scientific papers

SYNTHETIC STUDY ON APLYSIATOXINS, HIGHLY INFLAMMATORY AGENTS AND TUMOR PROMOTERS. SYNTHESIS OF THE THREE OPTICALLY ACTIVE SEGMENTS

The main segments in debromoaplysiatoxin and related aplysiatoxins have been efficiently synthesized from D-glucose and L- and D-tartaric acids.