97549-48-9

Upstream product

• 122480-81-3 5-Hydroxy-4-(4-hydroxy-phenyl)-6-methoxy-2-methyl-3,4-dihydro-2H-isoquinolin-1-one 
• 104517-01-3 4-benzyloxycinnamyl 2-methoxyphenyl ether 
• 90-05-1 2-methoxy-phenol 
• 87030-11-3 ethyl 3-(4-(benzyloxy)phenyl)acrylate 
• 87030-12-4 4-benzyloxycinnamyl alcohol 
• 122480-77-7 2-[(2,3-Dimethoxy-phenyl)-(4-methoxy-phenyl)-methyl]-malonic acid dimethyl ester 
• 122480-80-2 5,6-Dimethoxy-4-(4-methoxy-phenyl)-2-methyl-3,4-dihydro-2H-isoquinolin-1-one 
• 122480-79-9 5,6-Dimethoxy-4-(4-methoxy-phenyl)-3,4-dihydro-2H-isoquinolin-1-one 
• 104517-01-3 C₂₃H₂₂O₃ 
• 122480-78-8 3-(2,3-Dimethoxy-phenyl)-3-(4-methoxy-phenyl)-propionic acid 
• 122480-76-6 dimethyl 2-(2,3-dimethoxybenzylidene)malonate 
• 84184-52-1 (E)-3-(4-(benzyloxy)phenyl)prop-2-en-1-ol 
• 97456-07-0 rac-2-benzyloxy-β-(4-benzyloxyphenyl)-3-methoxy-N-methylphenethylamine 
• 97456-03-6 rac-2-benzyloxy-β-(4-benzyloxyphenyl)-3-methoxyphenethyl alcohol 

Relevant academic research and scientific papers

Total syntheses of (±)-cherylline and (±)-latifine

A new total synthesis of the two phenolic alkaloids (±)-cherylline 1 and (±)-latifine-2 isolated from Crinum species is described. The two key steps in the elaboration of these natural products are an anionic variant of the Fries rearrangement which gives

Synthesis of Amaryllidaceae Alkaloids, (+/-)-Cherylline and (+/-)-Latifine

Synthesis of the alkaloids, (+/-)-cherylline (1) and (+/-)-latifine (2), was accomplished by application of an isocyanate cyclization reaction according to Tsuda's two step procedure for constructing 1,2,3,4-tetrahydroisoquinol-1-one and a regioselective

Structure and Synthesis of a Novel Alkaloid, Latifine, from Crinum latifolium

A novel alkaloid, latifine, was isolated from leaves and bulbs of Crinum latifolium L. (Amaryllidaceae), and the structure (1) of the base was elucidated from spectral data, biogenetic considerations, X-ray analysis, and synthesis of its racemate.

Total Synthesis of (+/-)- and (+)-Latifine

Racemic latifine (+)-(1), a new representative of the rare phenolic Amaryllidaceae alkaloids, has been synthesized by employing the Claisen rearrangement of 4-benzyloxycinnamyl 2-methoxyphenyl ether (11) as a key step.Based on the racemic synthesis, (R)-(

THE TOTAL SYNTHESIS OF (+/-)-LATIFINE

Latifine, a novel phenolic isoquinoline base from Crinum latifolium L. (Amaryllidaceae), has been synthesized.