93741-07-2

Upstream product

• 86771-46-2 (+/-)-4-chloro-2-<(2'E,6'E)-7'-(3,3-dimethyl-4,4-ethylenedioxy-2-oxacyclopentyl)-3',7'-dimethyl-2',6'-heptadienyl>orcinol 
• 122-51-0 orthoformic acid triethyl ester 
• 86771-44-0 (+/-)-8-(7-bromo-1,5-dimethyl-1(E),5(E)-heptadienyl)-6,6-dimethyl-1,4,7-trioxaspiro<4.4>nonane 
• 86771-45-1 (+/-)-3-<(2'E,6'E)-7'-(3,3-dimethyl-4,4-ethylenedioxy-2-oxacyclopentyl)-3',7'-dimethyl-2',6'-heptadienyl>-1,5-dichloro-6-methyl-2,4-cyclohexanedione 
• 86855-29-0 (+/-)-3-<(2'E,6'E)-7'-(3,3-dimethyl-4,4-ethylenedioxy-2-oxacyclopentyl)-3',7'-dimethyl-2',6'-heptadienyl>-2,4-dimethoxy-6-methyl-1,4-cyclohexadiene 
• 86771-42-8 (+/-)-(2E,6E)-7-(3',3'-dimethyl-4',4'-ethylenedioxy-2'-oxacyclopentyl)-3,7-dimethyl-2,6-heptadienyl acetate 
• 95089-26-2 4,5-dihydro-5-[(1E,5E)-7-hydroxy-1,5-dimethyl-1,5-heptadienyl]-2,2-dimethyl-3(2H)-furanone 
• 86771-41-7 (+/-)-(2E,6E)-7-(3',3'-dimethyl-4'-oxo-2'-oxacyclopentyl)-3,7-dimethyl-2,6-heptadienyl acetate 
• 115-22-0 3-Hydroxy-3-methyl-2-butanone 
• 93741-06-1 (+/-)-methyl (E,E)-7-(6,6-dimethyl-1,4,7-trioxaspiro<4.4>non-8-yl)-3-methyl-2,6-octadienoate 
• 89983-26-6 ethyl (+/-)-(E)-3-(6,6-dimethyl-1,4,7-trioxaspiro<4.4>non-8-yl)-2-butenoate 
• 86771-43-9 (+/-)-(2E,6E)-7-(3',3'-dimethyl-4',4'-ethylenedioxy-2'-oxacyclopentyl)-3,7-dimethyl-2,6-heptadien-1-ol 
• 93741-02-7 (+/-)-(E)-3-(6,6-dimethyl-1,4,7-trioxaspiro<4.4>non-8-yl)-2-buten-1-ol 
• 93741-05-0 (+/-)-methyl (Z,E)-3-<(diethoxyphosphinyl)oxy>-7-(6,6-dimethyl-1,4,7-trioxaspiro<4.4>non-8-yl)-2,6-octadienoate 

Downstream Products

• 86832-77-1 dl-5-chloro-2,4-dihydroxy-6-methyl-3-[(2E,6E)-3-methyl-7-(3,3-dimethyl-4-oxo-2-oxacyclopentyl)-2,6-octadienyl]benzaldehyde 

Relevant academic research and scientific papers

Total Syntheses of Fungal Metabolites and Functionalized Furanones

Simple, efficient syntheses of the fungal metabolites colletochlorin D and (+/-)-ascofuranone and one of its stereoisomers are described.Our investigations of functionalized furanones also enabled us to develop a nine-step (22percent overall yield) synthe

SYNTHESIS OF (+/-)-ASCOCHLORIN, (+/-)-ASCOFURANONE AND LL-Z1272α

Three antibiotics with a common structural feature as prenylated phenols were synthesized: (+/-)-ascochlorin (5-chloro-2,4-dihydroxy-6-methyl-3-benzaldehyde), (+/-)-ascofurano

A SIMPLE TOTAL SYNTHESIS OF (+/-)-ASCOFURANONE

A simple, efficient total synthesis of (+/-)-ascofuranone is described.