96400-70-3

Upstream product

• 119123-67-0 methyl 4-(3-benzyloxy-4-methoxyphenyl)butyrate 
• 1403560-11-1 C₁₂H₁₆O₄ 
• 154490-53-6 2-(3,4-dimethoxyphenyl)-4-(3'-benzyloxy-4'-methoxy)phenyl butyric acid 
• 1064207-26-6 6-benzyloxy-7-methoxy-1-tetralone 
• 1403560-04-2 4-(3-benzyloxy-4-methoxyphenyl)butyric acid 
• 57596-01-7 4-(3-hydroxy-4-methoxyphenyl)butanoic acid 
• 1403560-03-1 4-(3-acetoxy-4-methoxyphenyl)-4-oxobutyric acid 
• 613-70-7 2-methoxyphenyl acetate 
• 96400-69-0 3-<4-benzyloxy-5-methoxy-2-(2,2-dimethoxyethyl)-phenyl>-6,7-dimethoxy-2-methylisoquinolin-1(2H)-one 
• 96400-68-9 3-(4-benzyloxy-5-methoxy-2-vinylphenyl)-6,7-dimethoxy-2-methylisoquinolin-1(2H)-one 

Downstream Products

• 113557-45-2 O-benzylfagaronine chloride 
• 52259-64-0 fagaronine 
• 96400-71-4 O-benzyldihydrofagaronine 

Relevant academic research and scientific papers

Synthesis of benzo[c]phenanthridine alkaloids by Pd(OAc) 2-induced direct aromatic carbonylation

The Pd(OAc)2-induced carbonylation of alkoxy-substituted 1-amino-2-phenyltetralins and 1-amino-2-phenylnaphthalenes was examined to provide the benzo[c]phenanthridine ring system. The carbonylation of substrates containing methylenedioxy groups

Total synthesis of oxyfagaronine, phenolic benzo[c]phenanthridine and general synthetic way of 2,3,7,8- and 2,3,8,9-tetrasubstituted benzo[c]phenanthridine alkaloids

Benzo[c]phenanthridine alkaloids such as oxynitidine, oxysanguinarine, oxyavicine and phenolic oxyfagaronine were synthesized from easily available starting benzonitriles 5 and toluamides 6 using a lithiated toluamidebenzonitrile cycloaddition reaction. T

TRANSFORMATION OF PROTOBERBERINES INTO BENZOPHENANTHRIDINES A NOVEL AND EFFICIENT SYNTHESIS OF ANTITUMOR BENZOPHENANTHRIDINE ALKALOIDS, FAGARONINE AND NITIDINE

Antileukemic benzophenanthridine alkaloids, fagaronine (1a) and nitidine (1c) were synthesized from the corresponding protoberberines through C6-N bond fission and subsequent cyclization between C6 and C13 position of the protoberberines.