62787-44-4

Upstream product

• 108-55-4 glutaric anhydride, 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 

Downstream Products

• 592512-28-2 (R)-phosphoric acid 6-oxo-1-(1-phenylethyl)-1,4,5,6-tetrahydropyridin-2-yl ester diphenyl ester 
• 592512-64-6 (+)-(3aR,4R,9aR,9bS)-4-butyl-2-phenyl-6-[(R)-1-phenylethyl]-4,6,8,9,9a,9b-hexahydro-3aH-pyrrolo[3,4-f]quinoline-1,3,7-trione 
• 592512-59-9 (+)-(3aR,9aR,9bS)-2-phenyl-6-[(R)-1-phenylethyl]-4,6,8,9,9a,9b-hexahydro-3aH-pyrrolo[3,4-f]quinoline-1,3,7-trione 
• 592512-48-6 (R)-(+)-6-(hex-1-ynyl)-1-(1-phenylethyl)-3,4-dihydro-1H-pyridin-2-one 
• 592512-45-3 (R)-(+)-1-(1-phenylethyl)-6-phenylethynyl-3,4-dihydro-1H-pyridin-2-one 
• 592512-39-5 (R)-(-)-1-(1-phenylethyl)-6-[(E)-styryl]-3,4-dihydro-1H-pyridin-2-one 

Relevant academic research and scientific papers

Preparation and cycloaddition reactions of enantiopure 2-(N-acylamino)-1,3-dienes for the synthesis of octahydroquinoline derivatives

Stille, Suzuki-Miyaura, and Sonogashira cross-coupling reactions were carried out with a glutarimide-derived vinyl phosphate, bearing a chiral auxiliary on the N atom, to prepare enantiopure 2-(N-acylamino)-1,3-dienes as partners in Diels-Alder reactions.