76504-08-0

Upstream product

• 22987-82-2 1-nitrocyclopentene 
• 54494-80-3 1-phenyl-2-(1-pyrrolidinyl)acetylene 

Downstream Products

• 76504-11-5 4-Phenyl-4-(pyrrolidine-1-carbonyl)-4a,5,6,7-tetrahydro-4H-3-oxa-3a-aza-cyclobuta[1,2:1,4]dicyclopentene-2-carboxylic acid methyl ester 
• 80996-36-7 methyl 5a,6,7,8-tetrahydro-5-phenyl-5-<(1-pyrrolidinyl)carbonyl>-5H-cyclopent<2,3>azeto<1,2-b>isoxazole-2-carboxylate 
• 80996-35-6 dimethyl 5a,6,7,8-tetrahydro-5-phenyl-5-<(1-pyrrolidinyl)carbonyl>-5H-cyclopent<2,3>azeto<1,2-b>isoxazole-1,2-dicarboxylate 
• 76504-10-4 4-Phenyl-4-(pyrrolidine-1-carbonyl)-4a,5,6,7-tetrahydro-4H-3-oxa-3a-aza-cyclobuta[1,2:1,4]dicyclopentene-1,2-dicarboxylic acid dimethyl ester 
• 76504-09-1 1-<(3a,4,5,6-tetrahydro-3-phenyl-3H-cyclopentisoxazol-3-yl)carbonyl>pyrrolidine 

Relevant academic research and scientific papers

Chemistry of Four-Membered Cyclic Nitrones. 1. Synthesis and Thermal Isomerization of 2,3-Dihydroazete 1-Oxides

Nitroalkenes (1) react with ynamines (1-aminoacetylenes, 2) to yield nitrocyclobutenes 3 and four-membered cyclic nitrones (2,3-dihydroazete 1-oxides, 5); in one case the open-chain isomer (4) of a four-membered cyclic nitrone was isolated.Nitrones 5 isom

(4+2)-CYCLOADDITION OF NITROALKENES WITH YNAMINES; FORMATION OF A 4H-1,2-OXAZINE 2-OXIDE DERIVATIVE

The formation of a thermally unstable (4+2)-cycloadduct, a 4H-1,2-oxazine 2-oxide derivative (1), from the reaction of 1-nitrocyclopentene with 1-phenyl-2-(1-pyrrolidinyl)acetylene has been proven by the structure elucidation of isoxazole derivative 3 whi