97345-59-0

Upstream product

• 94063-58-8 (5R)-1-benzoyl-5-benzylpyrrolidin-2-one 
• 97345-58-9 (8E,10E,12E)-1-imidazol-1-yl-12-methyltetradeca-8,10,12-trien-1-one 
• 97345-56-7 (8E,10E,12E)-methyl 12-methyltetradeca-8,10,12-trienoate 
• 97345-57-8 (8E,10E,12E)-12-methyltetradeca-8,10,12-trienic acid 
• 104701-95-3 (2E,4E)-4-Methylhexa-2,4-dienylphosphonic acid diethylester 
• 78289-06-2 1-methoxycyclooctene 
• 3884-92-2 methyl 8-oxooctanoate 

Downstream Products

• 97345-60-3 (8'E,10'E,12'E)-1-benzoyl-5-benzyl-3-(12'-methyl-1'-oxotetradeca-8',10',12'-trienyl)-3-phenylselenopyrrolidin-2-one 
• 97345-64-7 10-phenyl<11>cytochalasa-6(7),13^t-diene-1,21,-dione 
• 97345-63-6 2-benzoyl-10-phenyl<11>cytochalasa-6(7),13^t-diene-1,21,-dione 
• 97345-62-5 (5S,8'E,10'E,12'E)-1-benzoyl-5-benzyl-3-(12'-methyl-1'-oxotetradeca-8',10',12'-trienyl)pyrrol-2(5H)-one 

Relevant academic research and scientific papers

Cytochalasan Synthesis: Macrocycle Synthesis Using Intramolecular Diels-Alder Reactions. X-Ray Crystal Structure of 10-Phenylcytochalasa-6(7),13t-diene-1,21-dione

An approach to the total synthesis of cytochalasans has been developed which makes use of an intramolecular Diels-Alder reaction to close the large ring simultaneously forming the hydrogenated isoindolone unit with the desired stereochemistry.Conjugated t