Stereospecific [2π+2π+2π] Cycloaddition Reaction of Norbornadiene
- 1 October 1975
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 48 (10) , 2922-2926
- https://doi.org/10.1246/bcsj.48.2922
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- The π‐Orbital Sequence in Norbornadiene and Related HydrocarbonsHelvetica Chimica Acta, 1972
- Role of attractive interactions in endo-exo stereoselectivities of Diels-Alder reactionsJournal of the American Chemical Society, 1972
- Regio- and stereospecific [2.pi. + 2.sigma. + 2.sigma.] cycloaddition reaction of quadricyclaneJournal of the American Chemical Society, 1972
- Photoelectron Spectra of Bicyclic and Exocyclic OlefinsThe Journal of Chemical Physics, 1970
- Ionization Potential and Structure of OlefinsThe Journal of Chemical Physics, 1970
- Interaction of nonconjugated double bondsJournal of the American Chemical Society, 1970
- Photoelectron spectra of molecules. III. Ionization potentials of some cyclic hydrocarbons and their derivatives, and heats of formation and ionization potentials calculated by the MINDO[minimum neglect of differential overlap]SCF MO methodJournal of the American Chemical Society, 1970
- Bridged Polycyclic Compounds. XVIII. Addition of Dialkyl Azodicarboxylates to Norbornadiene1The Journal of Organic Chemistry, 1962
- Synthesis of Two Atom-Bridged Tetracyclic KetonesThe Journal of Organic Chemistry, 1960
- Synthesis of Some Conjugated Cyclobutane Polyolefins and their 1,2-Cycloaddition to Tetracyanoethylene1,2Journal of the American Chemical Society, 1959