66312-72-9

Upstream product

• 5153-67-3 nitrostyrene 
• 54781-35-0 ((1-(cyclohex-1-en-1-yl)vinyl)oxy)trimethylsilane 
• 75-52-5 nitromethane 
• 101183-80-6 (E)-1-(cyclohex-1-enyl)-3-phenylprop-2-en-1-one 
• 66312-71-8 1-cyclohexenyl-4-nitro-3-phenylbutan-1-one 
• 932-66-1 1-cyclohexenyl methyl ketone 
• 66312-68-3 4-(1-cyclohex-1-enyl-vinyl)-morpholine 
• 66312-72-9 (3S,4R,4aS,8aS)-4-Nitro-3-phenyl-octahydro-naphthalen-1-one 
• 66312-69-4 4-((3S,4S,4aR)-4-Nitro-3-phenyl-2,3,4,4a,5,6,7,8-octahydro-naphthalen-1-yl)-morpholine 

Downstream Products

• 66312-72-9 (3R,4R,4aR,8aR)-4-Nitro-3-phenyl-octahydro-naphthalen-1-one 

Relevant academic research and scientific papers

Substituent Effects on the Reactivity of 2-Morpholinobutadienes in the Presence of Dienophiles

2-Morpholinobutadienes (1) behave like typical enamines in their reactions with dimethyl acetylenedicarboxylate (2), β-nitrostyrene (3), diethyl 2-oxomalonate (4), and benzaldehyde (5).The nature of the resulting products is strongly dependent on the conf

SYNTHESIS OF NITRO-SUBSTITUTED DECALONES BY DOUBLE MICHAEL REACTION, SEQUENTIAL MICHAEL REACTION, AND BY DIELS ALDER REACTION

4-Nitro-3-phenyl-decalones are obtained from 1-acetylcyclohexene by three different ways.Stereochemistry and reaction pathways are discussed, and, for the first time, an intermediate of a sequential Michael reaction is isolated.