115477-11-7

Upstream product

• 1122-17-4 dichloromaleic acid anhydride 
• 115477-05-9 Benzyl-((2E,4E)-hexa-2,4-dienyl)-amine 
• 115477-05-9 benzyl[(2E,4E)-hexa-2,4-dien-1-yl]amine 
• 100-46-9 benzylamine 
• 63072-78-6 sorbyl bromide 

Downstream Products

• 122457-64-1 (3RS,6SR)-8-benzyl-3-methyl-9-oxo-8-azabicyclo<4.3.0>non-1-ene-2-carboxylic acid 
• 115477-12-8 (1RS,4SR)-8-benzyl-5-chloro-4-methyl-8-azabicyclo<4.3.0>nona-2,5-dien-7-one 
• 115477-28-6 (1RS,2SR,3SR,6RS)-8-benzyl-3-methyl-9-oxo-8-azabicyclo<4.3.0>non-4-ene-2-carboxylic acid 
• 122457-66-3 (1RS,4SR)-8-benzyl-5-chloro-4-methyl-8-azabicyclo<4.3.0>non-5-en-7-one 

Relevant academic research and scientific papers

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

New features of the intramolecular Diels Alder route to hydroisoindoles

Regio- and stereo- controlled routes to functionalised hydroisoindoles have been developed by reaction of aminodienes with unsaturated anhydrides or acid chlorides and subsequent elaboration of the Diels Alder adducts.