[1.n]Paracyclophane durch Vakuum‐Gasphasen‐Pyrolyse von Disulfonen
- 1 August 1978
- journal article
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 111 (8), 2997-3000
- https://doi.org/10.1002/cber.19781110828
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Orientierungseffekte auf Charge‐Transfer‐Wechselwirkungen, VI. Die beiden intramolekularen Chinhydrone der [2.2]Paracyclophan‐ReiheEuropean Journal of Inorganic Chemistry, 1977
- Steric effects in [2.2]metaparacyclophanes. Steric isotope effect, remote substituent effect on a steric barrier, and other steric phenomenaJournal of the American Chemical Society, 1974
- Das pseudogeminale „Chinhydron” der [2.2]Paracyclophan-ReiheAngewandte Chemie, 1974
- The Pseudogeminal “Quinhydrone” of the [2.2] Paracyclophane SeriesAngewandte Chemie International Edition in English, 1974
- Ein „intramolekulares Chinhydron”︁Angewandte Chemie, 1973
- An “Intramolecular Quinhydrone”Angewandte Chemie International Edition in English, 1973
- Transanulare Wechselwirkungen bei [2.2]Phanen, II. Synthesen von [2.2](4,4′)Biphenylophan, [2.2](2,7)Phenanthrenophan und [2](4,4′)Biphenylo[2](2,7)phenanthrenophanEuropean Journal of Inorganic Chemistry, 1973
- Transanulare Wechselwirkungen bei [2.2]Phanen, III. [2,2](2,6)Naphthalinophan und [2.2](2,6)Naphthalinophan‐1,11‐dienEuropean Journal of Inorganic Chemistry, 1973
- [2.2.2](1,3,5)Cyclophane and its derivatives. Extreme example of face-to-face crowding of aromatic ringsJournal of the American Chemical Society, 1973
- Unusually large conformational kinetic isotope effect in [2.2]metaparacyclophaneJournal of the American Chemical Society, 1972