89240-88-0

Upstream product

• 22231-61-4 2-[4-(benzyloxy)-3-methoxyphenyl]ethylamine 
• 7721-61-1 2-methyl-4-methoxy-5-hydroxybenzaldehyde 
• 89300-66-3 7-Acetoxy-1-(5-acetoxy-2-chloromethyl-4-methoxy-benzyl)-6-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid ethyl ester 
• 97400-60-7 2-methyl-4-methoxy-N-(4-benzyloxy-3-methoxyphenethyl)-5-benzyloxyphenylacetamide 
• 97400-59-4 2-methyl-4-methoxy-5-benzyloxybenzyl cyanide 
• 97400-62-9 5-(benzyloxy)-4-methoxy-2-methylbenzaldehyde 
• 97400-61-8 2-methyl-4-methoxy-5-benzyloxybenzyl alcohol 
• 97400-58-3 1-Benzyloxy-5-bromomethyl-2-methoxy-4-methyl-benzene 
• 60699-62-9 2-methyl-4-methoxy-5-benzyloxyphenylacetic acid 
• 1700-29-4 2-(4-(benzyloxy)-3-methoxyphenyl)acetonitrile 
• 33693-48-0 4-benzyloxy-3-methoxybenzyl alcohol 
• 72724-00-6 1-(benzyloxy)-4-(bromomethyl)-2-methoxybenzene 
• 7721-62-2 4,5-dimethoxy-2-methylbenzaldehyde 
• 494-99-5 1,2-dimethoxy-4-methylbenzene 

Relevant academic research and scientific papers

SYNTHESIS OF -2'-METHYLRETICULINE AND ITS INCORPORATION INTO ALKALOID FRACTIONS OF PAPAVER SOMNIFERUM

-2'-Methylreticuline has been synthesized by standard methods.This modified opium alkaloid precursor is efficiently incorporated by aberrant biosynthesis into alkaloid fractions of Papaver somniferum, particularly into a highly purified codeine fraction.Key Word Index - Papaver somniferum; Papaveraceae; morphine alkaloids; aberrant biosynthesis; 2'-methylreticuline.

SYNTHESIS OF 6'-METHYLATED RETICULINES AND TETRAHYDROPAPAVEROLINES

Racemic 6'-methylreticuline and the racemate and both enantiomers of 6'-methyl-N-norreticuline and 6'-methyltetrahydropapaveroline were synthesized from the appropriate isomers of coreximine diacetate (1).Reduction of crystalline chloromethylcarbamate 2 w