Publikācijas » 2017

Rezultātu skaits lapā  
Scopus datu bāzē indeksētās publikācijas
31Šmits G.; Audic B.; Wodrich M.D.; *Corminboeuf C.; Cramer N. A β-Carbon elimination strategy for convenient: In situ access to cyclopentadienyl metal complexes. Chem. Sci. 2017, 8(10), 7174-7179.      

32Kinēns A.; Sejejs M.; Kamlet A.S.; Piotrowski D.W.; Vedejs E.; *Suna E. Development of a chiral DMAP catalyst for the dynamic kinetic resolution of azole hemiaminals. J. Org. Chem. 2017, 82(2), 869-886.      

33Otikovs M.; Andersson M.; Jia Q.; Nordling K.; Meng Q.; Andreas L.B.; Pintacuda G.; Johansson J.; Rising A.; *Jaudzems K. Degree of Biomimicry of Artificial Spider Silk Spinning Assessed by NMR Spectroscopy. Angew. Chem. Int. Ed. 2017, 56(41), 12571-12575.      

34Skvorcova M.; *Jirgensons A. Intramolecular cyclopropylmethylation via non-classical carbocations. Org. Biomol. Chem. 2017, 15(33), 6909-6912.      

35Romanovs V.; Sidorkin V.; Belogolova E.; *Jouikov V. Radical cations of phenyl silatrane. Dalton Trans. 2017, 46(27), 8849-8854.      

36Nguyen T.T.; Grigorjeva L.; *Daugulis O. Aminoquinoline-directed, cobalt-catalyzed carbonylation of sulfonamide sp2 C-H bonds. Chem. Commun. 2017, 53(37), 5136-5138.      

37Grammatoglou K.; Bolsakova J.; *Jirgensons A. C-Quaternary alkynyl glycinols via the Ritter reaction of cobalt complexed alkynyl glycols. RSC Adv. 2017, 7(44), 27530-27537.      

38Bobiļeva O.; Ikaunieks M.; Duburs G.; Mandrika I.; Petrovska R.; Klovins J.; *Loža E. Synthesis and evaluation of (E)-2-(5-phenylpent-2-en-4-ynamido)cyclohex-1-ene-1-carboxylate derivatives as HCA2 receptor agonists. Bioorg. Med. Chem. 2017, 25(16), 4314-4329.      

39Zhao P.; Gvishi R.; Beķere L.; Lokshin V.; Khodorkovsky V.; Hagan D.J.; *Van Stryland E.W. Transient ring opening and closing of a two-photon photochromic molecule utilizing energy transfer. Opt.InfoBase Conf. Papers 2017, Part F41-CLEO_SI 2017.      

40Pustenko A.; Stepanovs D.; *Žalubovskis R.; Vullo D.; Kazaks A.; Leitans J.; Tars K.; Supuran C.T. 3H-1,2-benzoxathiepine 2,2-dioxides: a new class of isoform-selective carbonic anhydrase inhibitors. J. Enzyme Inhib. Med. Chem. 2017, 32(1), 767-775.      

Rezultātu skaits lapā