80902-00-7

Usage

InChI:InChI=1/C23H23ClO6/c1-13(2)23(26)17(8-15-9-18(24)21-19(10-15)28-12-29-21)22(25)30-20(23)11-14-4-6-16(27-3)7-5-14/h4-7,9-11,13,17,26H,8,12H2,1-3H3/b20-11-/t17-,23+/m0/s1

Upstream product

• 109292-79-7 (2R,3S)-2-(7-Chloro-benzo[1,3]dioxol-5-ylmethyl)-3-hydroxy-3-isopropyl-5-(4-methoxy-phenyl)-pent-4-ynoic acid 
• 34098-18-5 5-chloro-3,4-dihydroxybenzaldehyde 
• 19463-48-0 5-chlorovanillin 
• 88525-50-2 1-(4-methoxyphenyl)-4-methylpent-1-yn-3-ol 
• 88525-51-3 7-chlorobenzo[d][1,3]dioxole-5-carbaldehyde 
• 88525-49-9 1-(4-methoxyphenyl)-4-methylpent-1-yn-3-one 
• 88525-48-8 3-(7-Chloro-benzo[1,3]dioxol-5-yl)-propionic acid 
• 768-60-5 4-methoxyphenylacetylen 
• 109292-79-7 (2S,3S)-2-(7-Chloro-benzo[1,3]dioxol-5-ylmethyl)-3-hydroxy-3-isopropyl-5-(4-methoxy-phenyl)-pent-4-ynoic acid 
• 864152-64-7 4-isopropyl-5-[(E)-(4-methoxyphenyl)methylene]-3-[(3-chloro-4,5-methylenedioxyphenyl)methyl]-dihydro-2(3H)-furanone 
• 864152-61-4 4-isopropyl-5-[(Z)-(4-methoxyphenyl)methylene]-3-[(3-chloro-4,5-methylenedioxyphenyl)methyl]-dihydro-2(3H)-furanone 
• 18255-07-7 1-methoxy-4-<(phenylseleno)methyl>benzene 
• 824-94-2 p-methoxybenzyl chloride 
• 864152-58-9 (3R,4R,5R)-4-isopropyl-5-(l-menthyloxy)-3-[(3-chloro-4,5-methylenedioxyphenyl)methyl]-dihydro-2(3H)-furanone 

Relevant academic research and scientific papers

Synthesis and algicidal activity of (+)-cyanobacterin and its stereoisomer

(+)-Cyanobacterin, a photosynthesis inhibitor of freshwater cyanobacterium Schytonema hofmanni, was synthesized in 6 steps from a readily accessible chiral synthon 5R-5-(l-menthyloxy)-2(5H)furanone.

Total Synthesis and X-ray Structure Determination of Cyanobacterin

Racemic cyanobacterin has been synthesized and subjected to X-ray diffraction analysis in order to establish unambiguously the structure.