77960-30-6

Upstream product

• 100-46-9 benzylamine 
• 115477-07-1 (E)-N-benzylpenta-2,4-dien-1-amine 
• 68106-23-0 (Z)-3-carbomethoxy-2,3-dichloroacryloyl chloride 
• 122457-37-8 (Z)-methyl N-benzyl-N-3-<<(E)-penta-2,4-dienyl>carbamoyl>-2,3-dichloroacrylate 
• 122457-68-5 methyl hydrogen dichloromaleate 
• 4439-53-6 N-benzyl(furan-2-ylmethyl)amine 
• 4393-11-7 N-benzyl-1-(furan-2-yl)methanimine 
• 98-01-1 furfural 
• 67-56-1 methanol 
• 77960-29-3 2-benzyl-3-oxo-2,3-dihydro-1H-isoindole-5-carboxylic acid 
• 115477-32-2 (1RS,2SR,6SR)-methyl 8-benzyl-1,2-dichloro-9-oxo-8-azabicyclo<4.3.0>non-4-ene-2-carboxylate 
• 115477-32-2 (1RS,2SR,6RS)-methyl 8-benzyl-1,2-dichloro-9-oxo-8-azabicyclo<4.3.0>non-4-ene-2-carboxylate 

Relevant academic research and scientific papers

Synthesis of advanced intermediates of lennoxamine analogues

A simple and convenient method for synthesis of advanced isoindolone intermediates of lennoxamine and analogues is described in this paper. The intramolecular Diels-Alder reaction of furan is used as a key step in this synthesis. Georg Thieme Verlag Stuttgart.

Synthesis of Hydroisoindoles via Intramolecular Diels-Alder Reactions of Functionalised Amido Trienes

Reactions of amino dienes with acryloyl chloride, maleic anhydride, bromomaleic anhydride, and dichloromaleic anhydride were studied.Acylation and intramolecular reaction by Diels-Alder cyclisation gave bicyclic adducts.Adducts of dichloromaleic anhydride