Institut für Organische Chemie
Refine
Has Fulltext
- yes (316)
Is part of the Bibliography
- yes (316)
Year of publication
Document Type
- Journal article (316) (remove)
Keywords
- Organische Chemie (122)
- Chemie (9)
- water oxidation (9)
- 1 (8)
- fluorescence (8)
- self-assembly (8)
- 3 (7)
- RNA (7)
- photocatalysis (7)
- polycyclic aromatic hydrocarbons (7)
Institute
- Institut für Organische Chemie (316)
- Institut für Anorganische Chemie (16)
- Theodor-Boveri-Institut für Biowissenschaften (9)
- Institut für Virologie und Immunbiologie (8)
- Institut für Pharmazie und Lebensmittelchemie (6)
- Institut für Physikalische und Theoretische Chemie (5)
- Lehrstuhl für Tissue Engineering und Regenerative Medizin (5)
- Institut für Hygiene und Mikrobiologie (3)
- Physikalisches Institut (3)
- Institut für Funktionsmaterialien und Biofabrikation (2)
Sonstige beteiligte Institutionen
- Agricultural Center, BASF SE, 67117 Limburgerhof, Germany (1)
- Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells, Göttingen (1)
- Department of Cellular Biochemistry, University Medical Center Göttingen (1)
- Department of Cellular Biochemistry, University Medical Centre Göttingen (1)
- Department of Molecular Biology, University Medical Centre Göttingen (1)
- Georg August University School of Science (1)
- Göttingen Center for Molecular Biosciences, University of Göttingen (1)
- Helmholtz Institute for RNA-based Infection Biology (HIRI), Josef-Schneider-Straße 2/D15, DE-97080 Wuerzburg, Germany (1)
- Institut für Molekulare Infektionsbiologie (MIB) der Universität Würzburg (1)
- Institute of Cancer Research (ICR) London (1)
EU-Project number / Contract (GA) number
- 682586 (15)
- 787937 (14)
- 693023 (2)
- 242175-VascuBone (1)
- 242175‐VascuBone (1)
- 643238 (1)
- 654000 (1)
- 715923 (1)
- 949191 (1)
- LaserLab Europe (LLC001917) (1)
By means of the BC NMR spectra of tricyclo{2.2.0~rfJ6Jhexane and thirteen of its derivatives the effects of substituents in endo-3- and endo-5-positions on the HC chemical shifts have been determined. The y-anti effects are at least as Jarge as in monosubstituted cyc1obutanes, where the shielding values of second-row hetero substituents exceed those in unstrained systems by far, and higher-row and carbon substituents still cause substantial upfield shifts. In the title system the y-anti effect of a substituent in the endo-3- and endo-5-position are operative additively, and thus shift the absorption of C-J upfieJd by a maximum of 27 ppm with respect to the unsubstituted hydrocarbon.
No abstract available
7-Azatetracyclo[4.1.0.0<sup>2,4</sup>.0<sup>3,5</sup>]heptan - ein neues Valenzisomeres des Azepins
(1979)
No abstract available