Year |
Citation |
Score |
2024 |
Wiebe MA, Staubitz A, Manners I. Dehydrocoupling of Phosphine-Borane Adducts Under Ambient Conditions using Aminoboranes as Hydrogen Acceptors. Chemistry (Weinheim An Der Bergstrasse, Germany). e202403849. PMID 39672795 DOI: 10.1002/chem.202403849 |
0.443 |
|
2023 |
Di Tommaso EM, Walther M, Staubitz A, Olofsson B. -Functionalization of azobenzenes hypervalent iodine reagents. Chemical Communications (Cambridge, England). 59: 5047-5050. PMID 37038702 DOI: 10.1039/d3cc01060k |
0.581 |
|
2020 |
Li S, Eleya N, Staubitz A. Cross-Coupling Strategy for the Synthesis of Diazocines. Organic Letters. PMID 32009408 DOI: 10.1021/Acs.Orglett.0C00122 |
0.321 |
|
2020 |
Eleya N, Appiah C, Lork E, Gogolin M, Gesing TM, Stauch T, Staubitz A. Synthesis and Thermal Investigations of Eleven-Membered Ring Systems Containing One of the Heavier Group 14 Element Atoms Si, Ge, and Sn. Molecules. 25: 283. PMID 31936773 DOI: 10.3390/Molecules25020283 |
0.332 |
|
2020 |
Appiarius Y, Stauch T, Lork E, Rusch P, Bigall NC, Staubitz A. From a 1,2-azaborinine to large BN-PAHs via electrophilic cyclization: synthesis, characterization and promising optical properties Organic Chemistry Frontiers. DOI: 10.1039/D0Qo00723D |
0.327 |
|
2020 |
Dowds M, Bank D, Strueben J, Soto DP, Sönnichsen FD, Renth F, Temps F, Staubitz A. Efficient reversible photoisomerisation with large solvodynamic size-switching of a main chain poly(azobenzene-alt-trisiloxane) Journal of Materials Chemistry C. 8: 1835-1845. DOI: 10.1039/C9Tc05193G |
0.346 |
|
2019 |
Hoffmann J, Kuczmera TJ, Lork E, Staubitz A. Synthesis and crystal structure of (E)-1,2-bis-[2-(methyl-sulfan-yl)phen-yl]diazene. Acta Crystallographica Section E: Crystallographic Communications. 75: 1808-1811. PMID 31709113 DOI: 10.1107/S2056989019014592 |
0.363 |
|
2019 |
Urrego-Riveros S, Ramirez Y Medina IM, Duvinage D, Lork E, Sönnichsen FD, Staubitz A. Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31347203 DOI: 10.1002/Chem.201902255 |
0.34 |
|
2019 |
Hoffmann J, Kuczmera TJ, Lork E, Staubitz A. Synthesis, Structure, Thermal Behavior and cis/trans Isomerization of 2,2′-(EMe3)2 (E = C, Si, Ge, Sn) Substituted Azobenzenes Molecules. 24: 303. PMID 30650637 DOI: 10.3390/Molecules24020303 |
0.384 |
|
2019 |
Urrego-Riveros S, Bremer M, Hoffmann J, Heitmann A, Reynaldo T, Buhl J, Gates PJ, Sönnichsen FD, Hissler M, Gerken M, Staubitz A. Conjugated oligomers with alternating heterocycles from a single monomer: synthesis and demonstration of electroluminescence Organic Chemistry Frontiers. 6: 3636-3643. DOI: 10.1039/C9Qo00947G |
0.332 |
|
2018 |
Ramirez Y Medina IM, Rohdenburg M, Mostaghimi F, Grabowsky S, Swiderek P, Beckmann J, Hoffmann J, Dorcet V, Hissler M, Staubitz A. Tuning the Optoelectronic Properties of Stannoles by the Judicious Choice of the Organic Substituents. Inorganic Chemistry. PMID 30284825 DOI: 10.1021/Acs.Inorgchem.8B01649 |
0.309 |
|
2018 |
Staubitz A. Generation of High-Molecular-Weight Polymers with Diverse Substituents: An Unusual Metal-Free Synthesis of Poly(aminoborane)s. Angewandte Chemie. 57: 5990-5992. PMID 29717536 DOI: 10.1002/Anie.201801903 |
0.384 |
|
2018 |
Urrego‐Riveros S, Medina IRy, Hoffmann J, Heitmann A, Staubitz A. Syntheses and Properties of Tin-Containing Conjugated Heterocycles. Chemistry: a European Journal. 24: 5680-5696. PMID 28913884 DOI: 10.1002/Chem.201703533 |
0.358 |
|
2018 |
Staubitz A. Hochmolekulare Polymere mit diversen Substituenten durch eine ungewöhnliche, metallfreie Synthese von Poly(aminoboranen) Angewandte Chemie. 130: 6096-6098. DOI: 10.1002/Ange.201801903 |
0.332 |
|
2017 |
Thiedemann B, Gliese PJ, Hoffmann J, Lawrence PG, Sönnichsen FD, Staubitz A. High molecular weight poly(N-methyl-B-vinylazaborine) - a semi-inorganic B-N polystyrene analogue. Chemical Communications (Cambridge, England). PMID 28054054 DOI: 10.1039/C6Cc08599G |
0.385 |
|
2017 |
Schulz-Senft M, Gates PJ, Sönnichsen FD, Staubitz AC. Diversely halogenated spiropyrans: Useful synthetic building blocks for a versatile class of molecular switches Dyes and Pigments. 136: 292-301. DOI: 10.1016/J.Dyepig.2016.08.039 |
0.343 |
|
2016 |
Strüben J, Hoffmann J, Presa-Soto D, Näther C, Staubitz A. Crystal structures of 3,3′-bis(hydroxydimethylsilanyl)azobenzene and 4,4′-bis(hydroxydimethylsilane)azobenzene Acta Crystallographica Section E: Crystallographic Communications. 72: 1590-1594. PMID 27840715 DOI: 10.1107/S2056989016016297 |
0.335 |
|
2015 |
Strueben J, Lipfert M, Springer JO, Gould CA, Gates PJ, Sönnichsen FD, Staubitz A. High-yield lithiation of azobenzenes by tin-lithium exchange. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 11165-73. PMID 26118826 DOI: 10.1002/Chem.201500003 |
0.367 |
|
2015 |
He LY, Urrego-Riveros S, Gates PJ, Näther C, Brinkmann M, Abetz V, Staubitz A. Synthesis of poly(thiophene-alt-pyrrole) from a difunctionalized thienylpyrrole by Kumada polycondensation Tetrahedron. 71: 5399-5406. DOI: 10.1016/J.Tet.2015.05.091 |
0.347 |
|
2015 |
He LY, Schulz-Senft M, Thiedemann B, Linshoeft J, Gates PJ, Staubitz A. Nucleophile‐Selective Cross‐Coupling Reactions with Vinyl and Alkynyl Bromides on a Dinucleophilic Aromatic Substrate European Journal of Organic Chemistry. 2015: 2498-2502. DOI: 10.1002/Ejoc.201500138 |
0.349 |
|
2014 |
Linshoeft J, Näther C, Staubitz A. Crystal structure of 1,3-bis-(4-hexyl-5-iodo-thio-phen-2-yl)-4,5,6,7-tetra-hydro-2-benzo-thio-phene. Acta Crystallographica Section E-Structure Reports Online. 70. PMID 25484713 DOI: 10.1107/S1600536814019667 |
0.305 |
|
2014 |
Thiedemann B, Schmitz CML, Staubitz A. Reduction of N-allylamides by LiAlH4: unexpected attack of the double bond with mechanistic studies of product and byproduct formation. Journal of Organic Chemistry. 79: 10284-10295. PMID 25347383 DOI: 10.1021/Jo501907V |
0.359 |
|
2014 |
Linshoeft J, Baum EJ, Hussain A, Gates PJ, Näther C, Staubitz A. Highly tin-selective stille coupling: synthesis of a polymer containing a stannole in the main chain. Angewandte Chemie (International Ed. in English). 53: 12916-20. PMID 25258154 DOI: 10.1002/Anie.201407377 |
0.336 |
|
2014 |
Strueben J, Gates PJ, Staubitz A. Tin-Functionalized Azobenzenes as Nucleophiles in Stille Cross-Coupling Reactions Journal of Organic Chemistry. 79: 1719-1728. PMID 24502513 DOI: 10.1021/Jo402598U |
0.312 |
|
2013 |
Heinrich ACJ, Thiedemann B, Gates PJ, Staubitz A. Dual Selectivity: Electrophile and Nucleophile Selective Cross-Coupling Reactions on a Single Aromatic Substrate Organic Letters. 15: 4666-4669. PMID 23980843 DOI: 10.1021/Ol401923J |
0.354 |
|
2012 |
Linshoeft J, Heinrich ACJ, Segler SAW, Gates PJ, Staubitz A. Chemoselective Cross-Coupling Reactions with Differentiation between Two Nucleophilic Sites on a Single Aromatic Substrate Organic Letters. 14: 5644-5647. PMID 23121649 DOI: 10.1021/Ol302571T |
0.347 |
|
2012 |
Blackstone V, Pfirrmann S, Helten H, Staubitz A, Presa Soto A, Whittell GR, Manners I. A cooperative role for the counteranion in the PCl5-initiated living, cationic chain growth polycondensation of the phosphoranimine Cl3P═NSiMe3. Journal of the American Chemical Society. 134: 15293-6. PMID 22950530 DOI: 10.1021/Ja307703H |
0.677 |
|
2012 |
Helten H, Robertson AP, Staubitz A, Vance JR, Haddow MF, Manners I. "Spontaneous" ambient temperature dehydrocoupling of aromatic amine-boranes. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 4665-80. PMID 22392879 DOI: 10.1002/Chem.201103241 |
0.7 |
|
2012 |
Suárez SS, Soto DP, Carriedo GA, Soto AP, Staubitz A. Experimental and Theoretical Study of the Living Polymerization of N-Silylphosphoranimines. Synthesis of New Block Copolyphosphazenes Organometallics. 31: 2571-2581. DOI: 10.1021/Om201012G |
0.353 |
|
2011 |
Sloan ME, Staubitz A, Lee K, Manners I. Scope and selectivity of heterogeneous Rh0-catalyzed tandem dehydrocoupling/hydrogenation using Me2NH·BH 3 as a stoichiometric H2 source European Journal of Organic Chemistry. 672-675. DOI: 10.1002/Ejoc.201001332 |
0.491 |
|
2011 |
Robertson APM, Whittell GR, Staubitz A, Lee K, Lough AJ, Manners I. Experimental and theoretical studies of the potential interconversion of the amine-borane iPr2NH·BH(C6F5) 2 and the aminoborane iPr2N=B(C6F 5)2 involving hydrogen loss and uptake European Journal of Inorganic Chemistry. 5279-5287. DOI: 10.1002/Ejic.201100779 |
0.506 |
|
2010 |
Staubitz A, Sloan ME, Robertson AP, Friedrich A, Schneider S, Gates PJ, Schmedt auf der Günne J, Manners I. Catalytic dehydrocoupling/dehydrogenation of N-methylamine-borane and ammonia-borane: synthesis and characterization of high molecular weight polyaminoboranes. Journal of the American Chemical Society. 132: 13332-45. PMID 20806956 DOI: 10.1021/Ja104607Y |
0.527 |
|
2010 |
Staubitz A, Robertson AP, Manners I. Ammonia-borane and related compounds as dihydrogen sources. Chemical Reviews. 110: 4079-124. PMID 20672860 DOI: 10.1021/Cr100088B |
0.389 |
|
2010 |
Staubitz A, Robertson AP, Sloan ME, Manners I. Amine- and phosphine-borane adducts: new interest in old molecules. Chemical Reviews. 110: 4023-78. PMID 20672859 DOI: 10.1021/Cr100105A |
0.415 |
|
2010 |
Sloan ME, Staubitz A, Clark TJ, Russell CA, Lloyd-Jones GC, Manners I. Homogeneous catalytic dehydrocoupling/dehydrogenation of amine-borane adducts by early transition metal, group 4 metallocene complexes. Journal of the American Chemical Society. 132: 3831-41. PMID 20180565 DOI: 10.1021/Ja909535A |
0.437 |
|
2010 |
Bagh B, Gilroy JB, Staubitz A, Müller J. Ring-opening polymerization of a galla[1]ferrocenophane: a gallium-bridged polyferrocene with observable tacticity. Journal of the American Chemical Society. 132: 1794-5. PMID 20099824 DOI: 10.1021/Ja910648K |
0.596 |
|
2010 |
Herbert DE, Gilroy JB, Staubitz A, Haddow MF, Harvey JN, Manners I. Strain-induced cleavage of carbon-carbon bonds: bridge rupture reactions of group 8 dicarba[2]metallocenophanes. Journal of the American Chemical Society. 132: 1988-98. PMID 20095552 DOI: 10.1021/Ja9087049 |
0.711 |
|
2009 |
Herbert DE, Gilroy JB, Chan WY, Chabanne L, Staubitz A, Lough AJ, Manners I. Redox-active metallomacrocycles and cyclic metallopolymers: photocontrolled ring-opening oligomerization and polymerization of silicon-bridged [1]ferrocenophanes using substitutionally-labile Lewis bases as initiators. Journal of the American Chemical Society. 131: 14958-68. PMID 19772341 DOI: 10.1021/Ja904928C |
0.71 |
|
2009 |
Hamilton CW, Baker RT, Staubitz A, Manners I. B-N compounds for chemical hydrogen storage. Chemical Society Reviews. 38: 279-93. PMID 19088978 DOI: 10.1039/B800312M |
0.476 |
|
2008 |
Staubitz A, Presa Soto A, Manners I. Iridium-catalyzed dehydrocoupling of primary amine-borane adducts: a route to high molecular weight polyaminoboranes, boron-nitrogen analogues of polyolefins. Angewandte Chemie (International Ed. in English). 47: 6212-5. PMID 18613187 DOI: 10.1002/Anie.200801197 |
0.481 |
|
2008 |
Staubitz A, Besora M, Harvey JN, Manners I. Computational analysis of amine-borane adducts as potential hydrogen storage materials with reversible hydrogen uptake. Inorganic Chemistry. 47: 5910-8. PMID 18500797 DOI: 10.1021/Ic800344H |
0.456 |
|
2003 |
Dohle W, Staubitz A, Knochel P. Mild synthesis of polyfunctional benzimidazoles and indoles by the reduction of functionalized nitroarenes with phenylmagnesium chloride. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 5323-31. PMID 14613142 DOI: 10.1002/Chem.200305090 |
0.46 |
|
2003 |
Staubitz A, Dohle W, Knochel P. Expeditious Functionalization of Quinolines in Positions 2 and 8 via Polyfunctional Aryl- and Heteroarylmagnesium Intermediates Cheminform. 34. DOI: 10.1055/S-2003-36828 |
0.4 |
|
Show low-probability matches. |