80233-01-8

Upstream product

• 80233-00-7 3-((E)-But-2-enyl)-3-(3,4-dimethoxy-phenyl)-5-(1-hydroxy-ethyl)-dihydro-furan-2-one 
• 81309-83-3 (3S,5R)-3-((E)-But-2-enyl)-3-(3,4-dimethoxy-phenyl)-5-hydroxymethyl-dihydro-furan-2-one 
• 81309-82-2 (3R,5R)-5-Benzyloxymethyl-3-((E)-but-2-enyl)-3-(3,4-dimethoxy-phenyl)-dihydro-furan-2-one 
• 81309-78-6 (R)-5-Benzyloxy-2-(3,4-dimethoxy-phenyl)-4-hydroxy-pentanenitrile 
• 80232-99-1 3-((E)-But-2-enyl)-3-(3,4-dimethoxy-phenyl)-5-(1-iodo-ethyl)-dihydro-furan-2-one 
• 80232-98-0 (E)-2-((E)-But-2-enyl)-2-(3,4-dimethoxy-phenyl)-hex-4-enoic acid 
• 81309-80-0 (R)-5-Benzyloxymethyl-3-(3,4-dimethoxy-phenyl)-dihydro-furan-2-one 
• 93-17-4 3,4-dimethoxyphenylacetonitrile 

Downstream Products

• 81369-83-7 (S)-4-(3,4-Dimethoxy-phenyl)-4-(2-hydroxy-ethyl)-3-methylamino-cyclohex-2-enone 
• 81369-81-5 (3S)-(-)-3-(3,4-Dimethoxyphenyl)-3-(3-oxobutyl)tetrahydro-2-furanone 
• 81369-82-6 (S)-3a-(3,4-Dimethoxy-phenyl)-3,3a,4,5-tetrahydro-2H-benzofuran-6-one 
• 80233-04-1 (S)-3a-(3,4-Dimethoxy-phenyl)-3,3a,4,5-tetrahydro-2H-benzofuran-6-one 
• 468-53-1 (-)-mesembrine 
• 35714-44-4 Δ7-mesembrenone 
• 80233-02-9 (S)-3-((E)-But-2-enyl)-3-(3,4-dimethoxy-phenyl)-dihydro-furan-2-one 
• 80233-05-2 4-(3,4-Dimethoxy-phenyl)-4-(2-hydroxy-ethyl)-3-methylamino-cyclohex-2-enone 
• 80233-03-0 3-(3,4-Dimethoxy-phenyl)-3-(3-oxo-butyl)-dihydro-furan-2-one 
• 6023-73-0 mesembrine 
• 80287-15-6 3a-(3,4-dimethoxyphenyl)-1-methyl-3,3a,4,5-tetrahydro-1H-indol-6(2H)-one 
• 80233-02-9 3-((E)-But-2-enyl)-3-(3,4-dimethoxy-phenyl)-dihydro-furan-2-one 

Relevant academic research and scientific papers

ENANTIOSELECTIVE SYNTHESIS OF NATURAL MESEMBRINE USING (D)-MANNITOL AS A CHIRAL TEMPLATE, A MODEL STUDY FOR THE ENANTIOSELECTIVE SYNTHESIS OF THE AMARYLLIDACEAE ALKALOIDS

Enantioselective synthesis of (-)-mesembrine (1) has been achieved using (D)-mannitol with the intention of developing the enantioselective synthesis of the Amaryllidaceae alkaloids.

ANOTHER SYNTHESIS OF (+/-)-MESEMBRINE USING A SYMMETRIC STARTING MATERIAL

(+/-)-Mesembrine (10) has been synthesized efficiently via the vinylanalogous amide (9) using the symmetric substrate (1) as starting material.