104372-02-3

Upstream product

• 90-05-1 2-methoxy-phenol 
• 104315-02-8 (R)-(E)-1-benzyloxy-4-(4-benzyloxyphenyl)but-3-en-2-ol 
• 104315-04-0 (R)-(E)-6-<4-benzyloxy-1-(4-benzyloxyphenyl)but-2-enyl>guiacol 
• 104315-01-7 (S)-3-Benzenesulfinyl-1-benzyloxy-4-(4-benzyloxy-phenyl)-butan-2-ol 
• 104315-03-9 (S)-(E)-1-benzyloxy-4-(4-benzyloxyphenyl)but-3-en-2-yl 2-methoxyphenyl ether 
• 104315-08-4 (R)-(E)-4-benzyloxy-1-(4-benzyloxyphenyl)-1-(2-benzyloxy-3-methoxyphenyl)but-2-ene 
• 104371-96-2 (R)-2-benzyloxy-β-(4-benzyloxyphenyl)-3-methoxyphenethylamine 
• 104371-98-4 (R)-2-benzyloxy-β-(4-benzyloxyphenyl)-3-methoxyphenethyl alcohol 
• 104371-97-3 (R)-2-benzyloxy-β-(4-benzyloxyphenyl)-3-methoxy-N-methylphenethylamine 
• 104371-99-5 (R)-N-2-benzyloxy-<β-(4-benzyloxyphenyl)-3-methoxyphenethyl>formamide 
• 104371-95-1 (R)-N-2-benzyloxy-<β-(4-benzyloxyphenyl)-3-methoxyphenethyl>phthalimide 
• 104372-00-1 (R)-N-2-benzyloxy-<β-(4-benzyloxyphenyl)-3-methoxyphenethyl>-N-methylformamide 
• 568565-52-6 (2R)-N-[2-((2-isopropoxy-3-methoxy)phenyl)-4'-isopropoxyphenyl]ethyl-N-methylamine 
• 568565-47-9 (2-isopropoxy-3-methoxy-phenyl)-(4-isopropoxy-phenyl)-methanol 

Relevant academic research and scientific papers

Asymmetric synthesis of (+)- and (-)-latifine

A concise and novel synthesis of isoquinoline alkaloids (S)-latifine and of its antipode is reported. The key step relies on the stereoselective reduction of an appropriately substituted diarylenamine equipped with a chiral auxiliary followed by Pictet-Sp

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)-(