Aktuelle Publikationen (2014 - 2015)

291. D. Chaiyaveij, A.S. Batsanov, M.S. Fox, T.B. Marder, and A. Whiting, "An
        Experimental and Computational Approach to Understanding the Reactions of Acyl
        Nitroso Compounds in [4+2] Cycloadditions," J. Org. Chem., 80: 9518-9534 (2015).
        DOI: 10.1021/acs.joc.5b01470. Lesen Sie mehr...

290. S.K. Bose and T.B. Marder, "Metal-fee Catalytic Borylation of Carbon-Hydrogen 
        Bonds - A Leap Forward in C-H Functionalization," invited Perspective, Science,
        349: 473-474 (2015). DOI: 10.1126/science.aac9244. Lesen Sie mehr...

289. Z. Zhang, R.M. Edkins, M. Haehnel, M. Wehner, A. Eichhorn, L. Mailänder, M. Meier,
        J. Brand, F. Brede, K. Müller-Buschbaum, H. Braunschweig, and T.B. Marder,
        "Taming the Beast: Fluoromesityl Groups Induce a Dramatic Stability Enhancement 
        in Boroles," Chem. Sci., 6: 5922-5927 (2015). DOI: 10.1039/C5SC02205C.
        Lesen Sie mehr...

288. S.K. Bose, A. Deißenberger, A. Eichhorn, P.G. Steel, Z. Lin, and T.B. Marder, "Zinc-
        Catalyzed Dual C-X and C-H Borylation of Aryl Halides," Angew. Chem. Int. Ed., 54:
        11843-11847 (2015). DOI: 10.1002/anie.201505603. Angew. Chem. 127: 12009-
        12014 (2015). DOI: 10.1002/ange.201505603. Lesen Sie mehr...

287. N. Arnold, H. Braunschweig, P.B. Brenner, M. Ali Celik, R.D. Dewhurst, M. Haehnel,
        T. Kramer, I. Krummenacher, and T.B. Marder, "Correlations and Contrasts in Homo-
        Heteroleptic Cyclic (Alkyl)(amino)carbene (CAAC)-Containing Pt0 Complexes," Chem.
        Eur. J., 21: 12357-12362 (2015). DOI: 10.1002/chem.201502048.
        Lesen Sie mehr...

286. L. Ji, R.M. Edkins, A. Lorbach, I. Krummenacher, C. Brückner, A. Eichhorn, H.
        Braunschweig, B. Engels, P.J. Low, and T.B. Marder, "Electron Delocalization in
        Reduced Forms of 2-(BMes2)pyrene and 2,7-Bis(BMes2)pyrene," J. Am. Chem. Soc.,
        137: 6750-6753 (2015). DOI: 10.1021/jacs.5b03805. Lesen Sie mehr...

285. L. Ji, A. Lorbach, R.M. Edkins, and T.B. Marder, "Synthesis and Photophysics of a
        2,7-Disubstituted Donor-Acceptor Pyrene Derivative: An Example of the Application
        of Sequential Ir-Catalyzed C-H Borylation and Substitution Chemistry," J. Org. Chem.,
        80: 5658-5665 (2015. DOI: 10.1021/acs.joc.5b00618. Lesen Sie mehr...

284. S.A. Sadler, A. C. Hones, B. Roberts, D. Blakemore, T.B. Marder, and P.G. Steel,
        "Multidirectional Synthesis of Substituted Indazoles via Iridium-Catalyzed C-H
        Borylation," J. Org. Chem., 80: 5308-5314 (2015). DOI: 10.1021/acs.joc.5b00452.
        Lesen Sie mehr...

283. S. Pietsch, U. Paul, I.A. Cade, M.J. Ingleson, U. Radius, and T.B. Marder, "Room
        Temperature Ring Expansion of N-Heterocyclic Carbenes and B-B Bond Cleavage of
        Diboron(4) Compounds," Chem. Eur. J., 21: 9018-9021 (2015).
        DOI: 10.1002/chem.201501498. Lesen Sie mehr...

282. R.D. Dewhurst, E.C. Neeve, H. Braunschweig, and T.B. Marder, "sp²-sp³ Diboranes:
        Astounding Structural Variability and Mild Sources of Nucleophilic Boron for Organic
        Synthesis," Chem. Commun., 51: 9594-9607 (2015). (Featured Article).
        DOI: 10.1039/c5cc02316e. Lesen Sie mehr...

281. M.S. Cheung, F.K. Sheong, T.B. Marder, and Z. Lin, "Computational Insight into
        Nickel-Catalyzed Carbon-Carbon versus Carbon-Boron Coupling Reactions of
        Primary, Secondary and Tertiary Alkyl Bromides," Chem. Eur. J., 21: 7480-7488
        (2015). DOI: 10.1002/chem.201500110. (Designated as a Hot Paper).
        Lesen Sie mehr...

280. S. Pietsch, E.C. Neeve, D.C. Apperley, R. Bertermann, F. Mo, Di Qiu, M.S. Cheung, L.
        Dang, J. Wang, U. Radius, Z. Lin, C. Kleeberg, and T.B. Marder, "Synthesis, Structure
        and Reactivity of Anionic sp2-sp3 Diboron Compounds: Readily Accessible Boryl
        Nucleophiles," Chem. Eur. J., : 7082-7098 (2015). DOI: 10.1002/chem.201500235.
        (Designated as a Hot Paper). Lesen Sie mehr...

279. L. Ji, K. Fucke, S.K. Bose, and T.B. Marder, “Iridium-Catalyzed Borylation of Pyrene:
        Irreversibility and the Influence of Ligand on Selectivity,” J. Org. Chem., 80: 661-665
        (2015). Lesen Sie mehr...

278. Z. Zhang, R.M. Edkins, J. Nitsch, K. Fucke, A. Eichhorn, A. Steffen, Y. Wang, and
        T.B. Marder, “D-π-A Triarylboron Compounds with Tunable Push-Pull Character
        Achieved by Modification of Both the Donor and Acceptor Moieties,” Chem. Eur. J., 
        21: 177-190 (2015). DOI: 10.1002/chem.201405621. (Designated as a VIP – 
        Very Important Paper). Lesen Sie mehr...

277. Z. Zhang, R.M. Edkins, J. Nitsch, K. Fucke, A. Steffen, L.E. Longobardi,
        D.W. Stephan, C. Lambert and T.B. Marder, “ Optical and Electronic Properties
        of Air-stable Organoboron Compounds with Strongly Electron-accepting
        Bis(fluoromesityl)boryl Groups,” Chem. Sci., 6: 308-321 (2015).
        DOI: 10.1039/c4sc02410a  Lesen Sie mehr... 

276. Z.-Q. Zhang, C.-T. Yang, L.-J. Liang B. Xao, X. Lu, J.-H. Liu, Y.-Y. Sun, T.B. Marder,
        and Y. Fu, “Copper-Catalyzed/Promoted Cross-coupling of gem-Diborylalkanes
        with Nonactivated Primary Alkyl Halides: An Alternative Route to Alkylboronic
        Esters", Org. Lett., 16: 6342-6345 (2014). DOI: 10.1021/ol503111h.
       Lesen Sie mehr...

275. S.A. Sadler, H. Tajuddin, I.A.I. Mkhalid, A.S. Batsanov, D. Albesa-Jove,
        M.S. Cheung, A.C. Maxwell, L. Shukla, B. Roberts, D.C. Blakemore, Z. Lin,
        T.B. Marder, and P.G. Steel, “Iridium-Catalyzed C-H Borylation of Pyridines,”
        Org. Biomol. Chem., 12: 7318-7327 (2014). DOI: 10.1039/C4OB01565G
        Lesen Sie mehr...

274. S.K. Bose and T.B. Marder, “Efficient Synthesis of Aryl Boronates via Zinc-
        Catalyzed Cross-Coupling of Alkoxy Diboron Reagents with Aryl Halides at
        Room Temperature,” Org. Lett., 16: 4562-4565 (2014). DOI: 10.1021/ol502120q
        Lesen Sie mehr...

273. L. Ji, R.M. Edkins, L.J. Sewell, A. Beeby, A.S. Batsanov, K. Fucke, M. Drafz,
        J.A.K. Howard O. Moutounet, F. Ibersiene, A. Boucekkine, E. Furet, Z. Liu,
        J.-F. Halet, C. Katan, and T.B.Marder, “Experimental and Theoretical Studies
        of Quadrupolar Oligothiophene-cored Chromophores Containing Dimesitylboryl
        Moieties as π-Accepting End-groups: Syntheses,Structures, Fluorescence,
        One- and Two-photon Absorption,” Chem. Eur. J., 20: 13618 13635 (2014).
        DOI: 10.1002/chem.201402273. Lesen Sie mehr...

272. A. Steffen, K. Costuas, A. Boucekkine, M.-H. Thibault, A. Beeby, A.S. Batsanov,
        A. Charaf Eddin, D. Jacquemin, J.-F. Halet, and T.B. Marder, "Fluorescence in
        Rhoda- and Iridacyclopentadienes Neglecting the Spin-Orbit Coupling of the
        Heavy Atom: The Ligand Dominates" Inorg. Chem., 53: 7055-7069 (2014).
        DOI: 10.1021/ic501115k  Lesen Sie mehr...

271. X. Yin, J. Chen, R.A. Lalancette, T.B. Marder, and F. Jäkle, “Highly Electron-
        Deficient, Air Stable Conjugated Thienylboranes,” Angew. Chem. Int.
        Ed., 53: 9761-9765 (2014). DOI: 10.1002/anie.201403700.
        Lesen Sie mehr...

270. R. Dewhurst and T.B. Marder, “Cascades of Catalytic Selectivity,”
        invited News and Views paper,  Nature Chemistry, 6: 279-280 (2014).
        Lesen Sie mehr...

269. A. Steffen, R.M. Ward, M.G. Tay, R.M. Edkins, F. Seeler, M. van Leeuwen,
        L.-O. Pålsson, A. Beeby, A.S. Batsanov, J.A.K. Howard, and T.B. Marder,
        “Regiospecfic formation and Unusual Optical Properties of 2,5-Bis(arylethynyl
        rhodacyclopentadienes: A New Class of Luminescent Organometallics,”
        Chem. Eur. J., 20: 3652-3666 (2014). DOI:10.1002/chem.201304068. 
        Lesen Sie mehr...

268. R.E. Lopez-Real, J.J.R. Budge, T.B. Marder, A. Whiting, P.N. Hunt, and 
        S.A. Przyborski, “Application of Synthetic Photostable Retinoids Induces 
        Novel Limb and Facial Phenotypes During Chick Embryogenesis In Vivo,” 
        J. Anat., 224: 392-411 (2014). DOI: 10.1111/joa.12147. Lesen Sie mehr... 
        Corrigendum: J. Anat., 224: 529 (2014).  DOI: 10.1111/joa.12161. 

267. S. Konishi, S. Kawamorita, T. Iwai, P.G. Steel, T.B. Marder, and M. Sawamura, 
        “Site-Selective C-H Borylation of Quinolines at the C8 Position Catalyzed by a Silica
        Supported Phosphane-Iridium System,” Chem. Asian J., 9: 434-438 (2014). 
        DOI: 10.1002/asia.201301423 Lesen Sie mehr...

266. S.K. Bose, K. Fucke, L. Liu, P.G. Steel, and T.B. Marder, “Zinc-Catalyzed Borylation
        of Primary, Secondary and Tertiary Alkyl Halides with Alkoxy Diboron Reagents 
        at Room Temperature,” Angew. Chem. Int. Ed., 53: 1799-1803 (2014). 
        DOI: 10.1002/anie.201308855 (Designated as a Hot Paper).
        Lesen Sie mehr...

265. J.A. Foster, R.M. Edkins, G.J. Cameron, N. Coglin, K. Fucke, S. Ridgeway, 
        A.G. Crawford, T.B. Marder, A. Beeby, S.L. Cobb, and J.W. Steed, 
       “Blending Gellators to Tune Gel Structure and Probe Anion-Induced Disassembly,” 
        Chem. Eur. J., 20: 279-291 (2014). DOI: 10.1002/chem.201303153
        Lesen Sie mehr...