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- Heteroleptic complexes via solubility control: examples of Cu(ii), Co(ii), Ni(ii) and Mn(ii) complexes based on the derivatives of terpyridine and hydroxyquinoline. Maria Baskin, Natalia Fridman, Monica Kosa, Galia Maayan
, Dalton Trans.
, 2017
, 46
, 15330
- Construction of diverse CdII/ZnII coordination polymers based on 5-(quinolyl)tetrazolate generated via in situ hydrothermal synthesis. Li Ma, Naiqian Yu, Susu Chen, Hong Deng
, CrystEngComm
, 2013
, 15
, 1352
- Polycyclic N-heterocyclic compounds. Part 52.1 One-step syntheses of imidazo[1,5-a]pyridines, imidazo[1,5-a]quinolines and imidazo[5,1-a]isoquinolines by Vilsmeier reactions of pyridine-2-carbonitriles, quinoline-2-carbonitriles and isoquinoline-1-carbonitriles. Kenji Sasaki, Akifumi Tsurumori, Takashi Hirota
, J. Chem. Soc., Perkin Trans. 1
, 1998
, 3851
- Exploiting the “Lego brick” approach to predict accurate molecular structures of PAHs and PANHs. Hexu Ye, Silvia Alessandrini, Mattia Melosso, Cristina Puzzarini
, Phys. Chem. Chem. Phys.
, 2022
, 24
, 23254
- Some substitution reactions of thieno[3,2-f]quinoline. N. B. Chapman, K. Clarke, K. S. Sharma
, J. Chem. Soc. C
, 1970
, 2334
- Reissert compound chemistry. Part 5. Formation of pyrrolo[1,2-a]-quinolines and pyrrolo[2,1-a]isoquinolines. Barrie C. Uff, Ronald S. Budhram, Malcolm F. Consterdine, John K. Hicks, Brian P. Slingsby, John A. Pemblington
, J. Chem. Soc., Perkin Trans. 1
, 1977
, 2018
- A rationally designed metal-binding helical peptoid for selective recognition processes. Maria Baskin, Galia Maayan
, Chem. Sci.
, 2016
, 7
, 2809
- Palladium-catalyzed cyanation of aryl and heteroaryl iodides with copper(I) cyanide. Takao Sakamoto, Kazutoshi Ohsawa
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 2323
- Photoinitiated substitution reactions of 4-cyanopyridine and 2-cyanoquinoline with 2,3-dimethylbut-2-ene. Tullio Caronna, Sergio Morrocchi, Pietro Traldi, Bruno M. Vittimberga
, J. Chem. Soc., Chem. Commun.
, 1979
, 64a
- Copper catalysed direct amidation of methyl groups with N–H bonds. Yao Huang, Tieqiao Chen, Qiang Li, Yongbo Zhou, Shuang-Feng Yin
, Org. Biomol. Chem.
, 2015
, 13
, 7289