Tröger's base (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Tröger's base" in English language version.

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  • Julius Tröger (1887). "Ueber einige mittelst nascirenden Formaldehydes entstehende Basen". Journal für Praktische Chemie. 36 (1): 225–245. doi:10.1002/prac.18870360123.
  • Ostami (2017). "Facile preparation of Ʌ-shaped building blocks: Hünlich-base derivatization". Synlett. 28 (13): 1641–1645. doi:10.1055/s-0036-1588180. S2CID 99294625.
  • Spielman, M. A. (1935). "The Structure of Troeger's Base". J. Am. Chem. Soc. 57 (3): 583–585. doi:10.1021/ja01306a060.
  • Prelog, V.; Wieland, P. (1944). "Über die Spaltung der Tröger'schen Base in optische Antipoden, ein Beitrag zur Stereochemie des dreiwertigen Stickstoffs". Helvetica Chimica Acta. 27 (1): 1127–1134. doi:10.1002/hlca.194402701143.
  • Sergeyev Sergey, Diederich François (2006). "Semipreparative enantioseparation of Tröger base derivatives by HPLC". Chirality. 18 (9): 707–712. doi:10.1002/chir.20318. PMID 16845673.
  • Kaztami (2019). "Optically active and photoswitchable Tröger's base analogs". New Journal of Chemistry. 43 (20): 7751–7755. doi:10.1039/C9NJ01372E. S2CID 164362391.
  • Takuya; et al. (2018). "Modular Synthesis of Optically Active Tröger's Base Analogues". ChemPlusChem. 78 (12): 1510–1516. doi:10.1002/cplu.201300295. PMID 31986657.
  • Lacour; et al. (2017). "Stereoselective and Enantiospecific Mono and Bis C-H azidation of Tröger Bases. Insight on Bridgehead Iminium Intermediates and Application to Anion-Binding Catalysis". Chemistry – A European Journal. 23 (36): 8678–8684. doi:10.1002/chem.201700845. PMID 28406541.
  • Stephan Rigol; Lothar Beyer; Lothar Hennig; Joachim Sieler; Athanassios Giannis (2013). "Hünlich Base: (Re)Discovery, Synthesis, and Structure Elucidation after a Century". Organic Letters. 15 (6): 1418–1420. doi:10.1021/ol400357t. PMID 23470133.
  • Kazem-Rostami, M. (2017). "Design and synthesis of Ʌ-shaped photoswitchable compounds employing Tröger's base scaffold". Synthesis. 49 (6): 1214–1222. doi:10.1055/s-0036-1588913. S2CID 99913657.
  • Novruz G. Akhmedov; et al. (2019). "Molecular lambda shape light-driven dual switches: spectroscopic and computational studies of the photoisomerization of bisazo Tröger base analogs". Journal of Molecular Structure. 1178: 538–543. Bibcode:2019JMoSt1178..538K. doi:10.1016/j.molstruc.2018.10.071. S2CID 105312344.
  • K. R. Masoud and A. Moghanian (2017). "Hunlich base derivatives as photo-responsive Ʌ-shaped hinges". Organic Chemistry Frontiers. 4 (2): 224–228. doi:10.1039/C6QO00653A.
  • Pardo, C; Sesmilo, E; Gutiérrez-Puebla, E; Monge, A; Elguero, J; Fruchier, A (2001). "New Chiral Molecular Tweezers with a Bis-Tröger's Base Skeleton". Journal of Organic Chemistry. 66 (5): 1607–1611. doi:10.1021/jo0010882. PMID 11262103.
  • Zdeněk Kejíka; Tomáš Bříza; Martin Havlík; Bohumil Dolenský; Robert Kaplánek; Jarmila Králová; Ivan Mikula; Pavel Martásek; Vladimír Král (2016). "Specific ligands based on Tröger's base derivatives for the recognition of glycosaminoglycans". Dyes and Pigments. 134: 212–218. doi:10.1016/j.dyepig.2016.07.002.
  • Shejwalkar, Pushkar; Sedinkin, Sergey L.; Bauer, Eike B. (2011). "New amino-dithiaphospholanes and phosphoramidodithioites and their rhodium and iridium complexes". Inorganica Chimica Acta. 366 (1): 209–218. doi:10.1016/j.ica.2010.11.006.
  • Adrian, J. C.; C. S. Wilcox (1989). "Chemistry of synthetic receptors and functional group arrays. 10. Orderly functional group dyads. Recognition of biotin and adenine derivatives by a new synthetic host". Journal of the American Chemical Society. 111 (20): 8055–8057. doi:10.1021/ja00202a078.
  • Goswami, S; Ghosh, K; Dasgupta, S (2000). "Troger's Base Molecular Scaffolds in Dicarboxylic Acid Recognition". Journal of Organic Chemistry. 65 (7): 1907–1914. doi:10.1021/jo9909204. PMID 10774008.
  • Sergey Sergeyev; Delphine Didier; Vitaly Boitsov; Ayele Teshome; Inge Asselberghs; Koen Clays; Christophe M. L. Vande Velde; Aurélie Plaquet; Benoît Champagne (2010). "Symmetrical and Nonsymmetrical Chromophores with Tröger's Base Skeleton: Chiroptical, Linear, and Quadratic Nonlinear Optical Properties—A Joint Theoretical and Experimental Study". Chemistry – A European Journal. 16 (27): 8181–8190. doi:10.1002/chem.201000216. PMID 20533454.
  • Navrátilová, Tereza; Tatar, Ameneh; Havlík, Martin; Hajduch, Jan; Drozdová, Michaela; Gurung, Kshitij; Palatinus, Lukáš; Čejka, Jan; Sedláček, Jakub; Anzenbacher, Pavel; Dolenský, Bohumil (2022-11-18). "Preparation and Characterization of Metalloporphyrin Tröger's and Spiro-Tröger's Base Derivatives". The Journal of Organic Chemistry. 87 (22): 15178–15186. doi:10.1021/acs.joc.2c01716. ISSN 0022-3263.
  • Li, Zhong; Xu, Xiaoyong; Peng, Yanqing; Jiang, Zhaoxing; Ding, Chuanyong; Qian, Xuhong (2005). "An Unusual Synthesis of Tröger's Bases Using DMSO/HCl as Formaldehyde Equivalent". Synthesis (8): 1228–30. doi:10.1055/s-2005-861868.
  • Bosmani, Alessandro; Pujari, Sandip; Guenee, Laure; Besnard, Céline; Poblador Bahamonde, Amalia Isabel; Lacour, Jerome (2017). "Stereoselective and Enantiospecific Mono and Bis C-H azidation of Tröger Bases. Insight on Bridgehead Iminium Intermediates and Application to Anion-Binding Catalysis". Chemistry – A European Journal. 23 (36): 8678–8684. doi:10.1002/chem.201700845. PMID 28406541.

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  • Julius Tröger (1887). "Ueber einige mittelst nascirenden Formaldehydes entstehende Basen". Journal für Praktische Chemie. 36 (1): 225–245. doi:10.1002/prac.18870360123.