98473-63-3

Upstream product

• 59046-34-3 3-ethoxycarbonyl-2-phenyldioxopyrroline 
• 3240-11-7 Phenylacetylene-d1 
• 6911-81-5 (E)-β-deuteriostyrene 
• 21370-59-2 (Z)-β-deuteriostyrene 
• 98473-62-2 rel-(1S,5R)-6-deutero-5-ethoxycarbonyl-1,7-diphenyl-2-azabicyclo<3.2.0>hept-6-ene-3,4-dione 
• 98473-63-3 C₂₁H₁₈⁽²⁾HNO₄ 

Downstream Products

• 122184-86-5 5-deuterio-4-ethoxycarbonyl-3-hydroxy-6,7-diphenyl-1,5-dihydro-2H-azepin-2-one 
• 98473-63-3 (1S^*,5R^*,6S^*,7S^*)-6-deuterio-5-ethoxycarbonyl-1,7-diphenyl-2-azabicyclo<3.2.0>heptane-3,4-dione 
• 122184-92-3 (1S^*,5R^*,6S^*,7S^*)-6-deuterio-3-ethoxy-5-ethoxycarbonyl-1,7-diphenyl-2-azabicyclo<3.2.0>hept-2-en-4-one 
• 122184-92-3 (1S^*,5R^*,6R^*,7R^*)-6-deuterio-3-ethoxy-4-ethoxycarbonyl-1,7-diphenyl-2-azabicyclo<3.2.0>hept-2-en-4-one 

Relevant academic research and scientific papers

Dioxopyrrolines. XLII. Mechanism of 7-Epimerization Reaction of 7-Substituted 5-Ethoxycarbonyl-1-phenyl-2-azabicycloheptane-3,4-diones

7-Mono- and 7,7-disubstituted 5-ethoxycarbonyl-1-phenyl-2-azabicycloheptane-3,4-diones undergo epimerization at C-7 when treated with base.Experiments using the stereospecifically deuterium labeled compound 6 showed that the inversion of stereochem

Dioxopyrrolines. XXXVII. Stereochemical Pathways of Dioxopyrroline-Olefin Photocycloaddition. Stereochemical Selection Rule for the Photocycloaddition of Enone-Olefin Pairs

The photocycloaddition of 4-ethoxycarbonyl-5-phenyl-2H-pyrrole-2,3-dione 1 to (Z)- and (E)-d-styrenes proceeded in a stereoselective manner to give the compounds in which the styrene component added to 1 antarafacially as the major products.Including thes