39503-23-6

Upstream product

• 67-66-3 chloroform 
• 45497-73-2 aniline hydroiodide 
• 6937-96-8 2,6-dimethoxy-4-methylbenzaldehyde 
• 644-66-6 4-(3-formyl-2-hydroxy-4-methoxy-6-methylbenzoyloxy)-2-hydroxy-3,6-dimethylbenzoic acid 
• 64-19-7 acetic acid 
• 526-37-4 atranol 
• 77-78-1 dimethyl sulfate 
• 74-88-4 methyl iodide 
• 7446-70-0 aluminium trichloride 
• 71-43-2 benzene 
• 15918-53-3 formyl-3-hydroxy-2-methoxy-4-methyl-6-benzoate de methyle 
• 4179-19-5 1,3-dimethoxy-5-methylbenzene 
• 15918-51-1 acide formyl-3-hydroxy-2-methoxy-4-methyl-6-benzoique 
• 520-43-4 2-hydroxy-4-methoxy-6-methyl-benzoic acid methyl ester 

Downstream Products

• 114561-50-1 acide hydroxy-2-methoxy-6-methyl-4-benzoique 
• 118975-29-4 acide dichloro-3,5-hydroxy-2-methoxy-6-methyl-4-benzoique 
• 4356-38-1 acide decarboxythamnolique 
• 57439-15-3 hydroxy-2-methoxy-6-methyl-4-benzoate de benzyle 
• 57439-18-6 formyl-3-hydroxy-2-methoxy-6-methyl-4-benzoate de benzyle 
• 57439-21-1 acide (benzyloxycarbonyl)-3-hydroxy-2-methoxy-4-methyl-6-benzoique 
• 118975-22-7 acide formyl-3-hydroxy-2-methoxy-6-methyl-4-benzoique 
• 118975-24-9 (benzyloxycarbonyl)-3-hydroxy-2-methoxy-4-methyl-6-benzoate de formyl-3-dihydroxy-2,4-methyl-6-phenyl 
• 1159012-12-0 3-(2-chlorobenzyl)-5-methoxy-7-methyl-2H-chromen-2-one 
• 1159012-10-8 5-methoxy-7-methyl-3-(2-methylbenzyl)-2H-chromen-2-one 
• 1159012-13-1 3-(4-chlorobenzyl)-5-methoxy-7-methyl-2H-chromen-2-one 
• 1159012-17-5 3-(2,4-dimethoxybenzyl)-5-methoxy-7-methyl-2H-chromen-2-one 
• 1159012-14-2 3-(2-hydroxybenzyl)-5-methoxy-7-methyl-2H-chromen-2-one 
• 1159012-15-3 5-methoxy-3-(3-methoxybenzyl)-7-methyl-2H-chromen-2-one 

Relevant academic research and scientific papers

N-CONTAINING CHROMEN-4-ONE DERIVATIVES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

The present invention provides the compounds having the general formula: (I) wherein R1 to R8, and X are as described herein, compositions including the compounds and methods of using the compounds.

Organocuprate-initiated domino Michael-intramolecular aldol reaction-Application to the formation of ring B of the aglycon of landomycins

An innovative access to a β,β-disubstituted Morita-Baylis-Hillman motif, which is a potential intermediate en route to the synthesis of the aglycon of landomycins, is presented. It consists of a finely optimized organocuprate-initiated domino Michael-intr

The total synthesis of the fungal metabolite diversonol

(Chemical Equation Presented) Mission accomplished. The fungal metabolite diversonol has been synthesized for the first time. A key step in the total synthesis was the domino oxa-Michael-aldol condensation of salicylic aldehyde 1 and 4-hydroxycyclohexenon

Regioselective demethylation of 2,6-dimethoxybenzaldehydes with magnesium iodide etherate

Demethylation of asymmetically substituted 2,6-dimethoxybenzaldehydes with magnesium iodide etherate regioselectively single 6-methoxysalicylaldehydes derived from the more unstable chelation.