679433-33-1

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 6248-20-0 2,4-dihydroxy-3-methylbenzaldehyde 
• 926-62-5 isobutylmagnesium bromide 
• 5674-02-2 2-methylpropylmagnesium chloride 

Downstream Products

• 679433-34-2 2-[3-hydroxy-2-methyl-6-(3-methyl-butyl)-phenoxy]-1-pyrrolidin-1-yl-ethanone 
• 919111-03-8 2-[3-hydroxy-2-methyl-6-(3-methyl-butyl)-phenoxy]-N-methoxy-N-methyl-propionamide 
• 919111-06-1 (2S,4R)-5-Benzyloxy-4-hydroxy-2-methyl-4-(3-methyl-butyl)-4H-anthracene-1,3-dione 
• 919111-05-0 11-benzyloxy-3,5-dimethyl-12b-(3-methyl-butyl)-12bH-1,4-dioxa-benzo[a]anthracene-2,6-dione 
• 919111-11-8 11-benzyloxy-3,5-dimethyl-12b-(3-methyl-butyl)-12a,12b-dihydro-12H-1,4-dioxa-benzo[a]anthracene-2,6-dione 
• 919111-07-2 Diethyl-carbamic acid (R)-5-benzyloxy-4-hydroxy-2-methyl-4-(3-methyl-butyl)-3-oxo-3,4-dihydro-anthracen-1-yl ester 
• 919111-08-3 (1R,2R)-8-Benzyloxy-2-(1-ethoxy-vinyl)-3-methyl-1-(3-methyl-butyl)-1,2-dihydro-anthracene-1,2,4-triol 

Relevant academic research and scientific papers

Total synthesis of (+)-rishirilide B: Development and application of general processes for enantioselective oxidative dearomatization of resorcinol derivatives

A concise synthesis of (+)-rishirilide B (2) is described. This is the first synthesis to be reported for the (+)-enantiomer of rishirilide B (2) as found in nature. The strategy accentuates the valuable combination of a method for oquinone methide coupli

Cycloadditions of o-quinone dimethides with p-quinol derivatives: Regiocontrolled formation of anthracyclic ring systems

Regioselective cycloadditions between the cyclohexadienones 12-14 and the ortho-quinone dimethide 19, which is thermally generated from the corresponding 1,3-dihydro-1-methoxy-2,2-dioxide benzo[c]thiophene 27, are reported. The synthetic sequence provides