93059-53-1

Upstream product

• 92973-98-3 anti-7-tert-butylbicyclo<2.2.1>heptane-2,3-dione 
• 92973-86-9 anti-7-tert-butylbicyclo<2.2.1>heptan-2-one 
• 91900-53-7 7-isopropylidenebicyclo<2.2.1>heptan-2-one 
• 92973-99-4 anti-7-isopropylbicyclo<2.2.1>heptane-2,3-dione, (Z)-monotosylhydrazone 
• 92973-96-1 anti 7-isopropylbicyclo<2.2.1>heptane-2,3-dione 
• 92973-80-3 anti-7-isopropylbicyclo<2.2.1>heptan-2-one 
• 542-92-7 cyclopenta-1,3-diene 
• 87371-52-6 endo-2-acetoxy-7-isopropylidenebicyclo<2.2.1>hept-5-ene-exo-2-carbonitrile 
• 37939-82-5 7,7-Isopropylidenebicyclo<2.2.1>hept-5-en-2-one 
• 2175-91-9 6,6'-dimethyl fulvene 
• 92973-99-4 anti-7-isopropylbicyclo<2.2.1>heptane-2,3-dione, (Z,E)-monotosylhydrazone 
• 92973-85-8 anti-7-isopropylbicyclo<2.2.1>heptan-2-one-2,4-dinitro-phenylhydrazone 
• 92973-81-4 endo-2-chloro-7-isopropylidenebicyclo<2.2.1>hept-5-ene-exo-2-carbonitrile 
• 92973-83-6 endo-2-chloro-7-isopropylidenebicyclo<2.2.1>heptane-exo-2-carbonitrile 

Relevant academic research and scientific papers

Aliphatic diazo compounds. XIV. The synthesis of 7-substituted 3-diazo-2-norbornanones and the infrared and proton and carbon-13 nuclear magnetic resonance spectra of these diazo ketones and their precursors

syn and anti-7-Isopropyl-2-norbornanone (5 and 6) were prepared by catalitic hydrogenation of 7-isopropylidene-2-norbornanone; syn and anti-7-benzhydryl-2-norbornane (9 and 10) were prepared in analogous fashion.Ketones 5 and 6 and syn- and anti-7-tert-bu

THE ACID INDUCED DECOMPOSITION OF 7-SUBSTITUTED 3-DIAZO-2-NORBORNANONES.THE STRUCTURES OF THE PRODUCTS AND THEIR DISTRIBUTION

Introduction of a syn-7 isopropyl or t-butyl substituent in 3-diazo-2-norbornanone results in both endo and exo protonation in aqueous acid and a marked decrease in α-ketol and increase in tricyclanone formation.