First attempts at differential diastereoselection in catalytic reactions of N-chirally substituted dirhodium(II) tetrakis[methyl 2-oxoimidazolidine-4(S)-carboxylates] with diazoacetates.
M. P. Doyle, D. J. Timmons, M. M. R. Arndt, A. Duursma, J. T. Colyer, H. Brunner, Russ. Chem. Bull., Int. Ed. 2001, 50, 2156-2161.
Platin(II)-Komplexe mit Porphyrinliganden: Synthese und Synergismen bei der photodynamischen Tumortherapie.
H. Brunner, H. Obermeier, R.-M. Szeimies, Chem. Ber. 1995, 128, 173-181.
Synthesis and in vitro testing of hematoporphyrin type ligands in platinum(II) complexes as potent cytostatic and phototoxic antitumor agents.
H. Brunner, K.-M. Schellerer, B. Treittinger, Inorg. Chim. Acta 1997, 264, 67-79.
Chiralitätsmultiplikation. Enantioselektive Katalyse mit Übergangsmetallkomplexen.
H. Brunner, GIT Fachz. Lab. 1994, 38, 273-277.
Dendrizymes: Expanded ligands for enantioselective catalysis.
H. Brunner, J. Organomet. Chem. 1995, 500, 39-46.
Right or Left in Chemistry - Enantioselective Catalysis with Transition Metal Compounds.
H. Brunner, Quim. Nova 1995, 18, 603-607.
Homogeneous Enantioselective Catalysis.
H. Brunner, Chiral React. Heterog. Catal., (Proc. Eur. Symp.), 1st (1993) (Publ. 1995), 29-32.
In Situ Catalysts in Enantioselective Catalysis with Transition-Metal Compounds.
H. Brunner, W. Zettlmeier, Adv. Catal. Processes (Asym. Chem. Transform.) 1995, 1, 1-27.
Optically Active Binaphthyl-Derived Salicylaldehydes and Salicylaldimines. Syntheses and Catalysis.
H. Brunner, Stereosel. React. Met.-Act. Mol., Proc. Symp., 2nd 1994 (Publ. 1995), 73-80.
Optically Active Transition Metal Compounds Containing Chiral Transition Metal Atoms.
H. Brunner, NATO ASI Ser., Ser. E 320 1996, 91-111.
Enantioselective Catalysis with Transition-Metal Complexes.
H. Brunner, NATO ASI Ser., Ser. E 320 1996, 175-190.
Hydrogenation.
H. Brunner, Appl. Homogeneous Catal. Organomet. Compd. 1996, 1, 201-219.
Enantioselective Catalysis; Part 93: Optically Active Expanded Phosphanes Derived from 1,2-Bisphosphanobenzene and Amides and Esters of Acrylic Acid.
H. Brunner, G. Net, Synthesis 1995, 423-426.
Enantioselective Catalysis 94. The "Diphenyl Effect" in the Enantioselective Hydrosilylation of Acetophenone with Diphenylsilane Using Rh/5,5-Diphenyl-2-(2-pyridinyl)oxazoline Catalysts.
H. Brunner, C. Henrichs, Tetrahedron: Asymmetry 1995, 6, 653-656.
Enantioselective Catalysis 95. An Asymmetric Hydrogenation System Breeding Its Own Counter-configurated Ligand.
H. Brunner, A. Terfort, Tetrahedron: Asymmetry 1995, 6, 919-922.
Enantioselektive Katalyse, 96. Naphthalin-Aufbauglieder in der Synthese von optisch aktiven Zweischalenphosphinen.
H. Brunner, J. Berghofer, Z. Naturforsch. 1995, 50b, 1510-1512.
Enantioselektive Katalyse 97. Optisch aktive Salicyloxazolin-Liganden in der enantioselektiven Kupfer-katalysierten Cyclopropanierung.
H. Brunner, J. Berghofer, J. Organomet. Chem. 1995, 501, 161-166.
Enantioselective Catalysis 98. Preparation of 9-Amino(9-deoxy)cinchona Alkaloids.
H. Brunner, J. Bügler, B. Nuber, Tetrahedron: Asymmetry 1995, 6, 1699-1702.
Enantioselective catalyses. Part 99. Phosphane ligands with two binding sites of differing hardness for enantioselective Grignard cross coupling.
A. Terfort, H. Brunner, J. Chem. Soc., Perkin Trans. 1 1996, 1467-1479.
Enantioselective Catalysis, C. Decarboxylation of Malonic Acids in the Presence of Copper(I) Compounds - Not a Copper(I) Catalysis but a Base Effect.
H. Brunner, J. Müller, J. Spitzer, Monatsh. Chem. 1996, 127, 845-858.
Enantioselective Catalysis, 101. Synthesis and Coordination Properties of (3'S,4'S)-(+)-1,2-Bis(3',4'-dimethoxyphospholano)benzene, a New Chiral Diphosphane.
H. Brunner, G. Net, Z. Naturforsch. 1996, 51b, 1210-1212.
Asymmetric Catalysis. Part 103. Enantioselective Michael Addition of 1,3-Dicarbonyl Compounds to Conjugated Nitroalkenes.
H. Brunner, B. Kimel, Monatsh. Chem. 1996, 127, 1063-1072.
Enantioselective Catalysis. Part 106. 9-Amino(9-deoxy)cinchona-Alkaloids and Their Derivatives.
H. Brunner, J. Bügler, Bull. Soc. Chim. Belg. 1997, 106, 77-84.
Enantioselective Catalysis. Part 107. New Optically Active Deltacyclenes as Building Blocks for the Synthesis of Expanded Phosphanes.
H. Brunner, A. Reimer, Bull. Soc. Chim. Fr. 1997, 134, 307-314.
Asymmetric Catalysis. Part 108. Copper Catalysts with Optically Active Ligands in the Enantioselective Meerwein Arylation of Activated Olefins.
H. Brunner, C. Blüchel, M. P. Doyle, J. Organomet. Chem. 1997, 541, 89-95.
Enantioselective Catalysis. Part 109. New Expanded Chiral Bipyridines.
H. Brunner, I. Poleschak, Z. Naturforsch., B: Chem. Sci. 1997, 52, 839-846.
Enantioselective Catalysis. Part 110. New Chiral Phosphanes Derived from Substituted Quinolines.
H. Brunner, T. Rückert, Synthesis 1997, 1309-1314.
Enantioselective Catalysis. Part 111. New Chiral Expanded Phosphanes Derived from Substituted Deltacyclenes.
H. Brunner, A. Reimer, Chem. Ber./Recl. 1997, 130, 1495-1498.
Enantioselective Catalysis. Part 112. New Chiral Deltacyclane-Based Tertiary Alcohols as Hydroperoxide Precursors.
H. Brunner, A. Reimer, Bull. Soc. Chim. Belg. 1997, 106, 267-272.
Enantioselective Catalysis. Part 113. New Menthylphosphane Ligands Differing in Steric and Electronic Properties.
H. Brunner, M. Janura, Synthesis 1998, 45-55.
Asymmetric Catalysis. Part 116. Triaza and Tetraaza Macrocycles with Chiral Pendant Arms in the Enantioselective Cyclopropanation.
H. Brunner, A. Winter, B. Nuber, Z. Naturforsch., B: Chem. Sci. 1997, 52, 1436-1438.
Asymmetric Catalysis. Part 117. Novel Chiral Oxazoline Ligands for Potential Charge-Transfer Effects in the Rh(I)-Catalyzed Enantioselective Hydrosilylation.
H. Brunner, R. Störiko, F. Rominger, Eur. J. Inorg. Chem. 1998, 771-781.
Asymmetric Catalysis. Part 118. Rh(I)-Catalyzed Asymmetric Hydrosilylation Using New Oxazoline Ligands with Potential Charge-Transfer Properties.
H. Brunner, R. Störiko, Eur. J. Inorg. Chem. 1998, 783-788.
Enantioselective Catalysis. Part 119. New Chiral 2-(2-Pyridinyl)oxazoline Ligands Containing an Additional Optically Active Substituent in the Pyridine System.
H. Brunner, R. Störiko, B. Nuber, Tetrahedron: Asymmetry 1998, 9, 407-422.
Enantioselective Catalysis. Part 120. New Optically Active Pyrrole-oxazolines.
H. Brunner, B. Haßler, Z. Naturforsch., B: Chem. Sci. 1998, 53, 476-480.
Enantioselective Catalysis. Part 121. Chiral Phosphane Ligands with Additional Oxygen Functionalities.
H. Brunner, T. Rückert, Monatsh. Chem. 1998, 129, 339-354.
Enantioselective Catalysis; 123: Octaaldehyde Type Chelating Ligands - A Divergent Synthesis Approach to Easily Tunable Expanded Ligands for Enantioselective Catalysis.
H. Brunner, M. Janura, S. Stefaniak, Synthesis 1998, 1742-1749.
Enantioselective Catalyses; 126: Axially Chiral N,N-Ligands with Binaphthyl/Bipyridyl Structure.
H. Brunner, G. Olschewski, B. Nuber, Synthesis 1999, 429-434.
Enantioselective Catalysis; 130: Optically Active Expanded Ligands Based on the trans-1,2-Substituted Cyclopentane Skeleton.
H. Brunner, S. Stefaniak, M. Zabel, Synthesis 1999, 1776-1784.
The First Helical-Chiral Phosphane Ligands: rac-[5]- and rac-[6]-Heliphos.
A. Terfort, H. Goerls, H. Brunner, Synthesis 1997, 79-86.
Synthesis, properties, stereochemistry and crystal structures of diastereomeric benzene-ruthenium(II) complexes with a chiral salicylideneaminato ligand. Optically Active Transition Metal Complexes. Part 107.
H. Brunner, R. Oeschey, B. Nuber, J. Chem. Soc., Dalton Trans. 1996, 1499-1508.
Optically active transition metal complexes. Part 108. Synthesis, crystal structure and properties of a novel "quasi-meso" dinuclear η6-benzene-ruthenium(II) complex with chiral salicylaldiminato ligands.
H. Brunner, R. Oeschey, B. Nuber, J. Organomet. Chem. 1996, 518, 47-53.
Optically Active Transition Metal Complexes. 109. Novel (η6-Benzene)ruthenium Complexes with a Chiral Pyrrolecarbaldiminato Chelate Ligand: Synthesis, Crystal Structures, Properties, and Stereochemistry at the Ruthenium Atom.
H. Brunner, R. Oeschey, B. Nuber, Organometallics 1996, 15, 3616-3624.
Optically active transition metal complexes 110. New rhodium(I) complexes with 2-pyridinecarboxamido ligands.
H. Brunner, B. Nuber, M. Prommesberger, J. Organomet. Chem. 1996, 523, 179-185.
Silver(I) Complexes with [(C5H5)2MoH2] and [(C5H5)2WH2] Ligands.
H. Brunner, M. Muschiol, T. Neuhierl, B. Nuber, Chem. Eur. J. 1998, 4, 168-171.
Optically Active Organometallic Compounds of Transition Elements with Chiral Metal Atoms.
H. Brunner, Angew. Chem. Int. Ed. 1999, 38, 1194-1208; Angew. Chem. 1999, 111, 1248-1263.
Comparative studies in the Cp2M(η2-S2)H series (Cp = t-BuC5H4, C5Me4Et; M = Nb, Ta) on the reactivity of hydride and disulfide ligands.
J.-C. Leblanc, C. Moïse, F. Volpato, H. Brunner, G. Gehart, J. Wachter, B. Nuber, J. Organomet. Chem. 1995, 485, 237-242.
Chemical evidence for the existence of peralkylated niobocene in a fulvenoid form by its reaction with sulfur.
H. Brunner, G. Gehart, W. Meier, J. Wachter, T. Burgemeister, J. Organomet. Chem. 1995, 493, 163-166.
Heterobimetallic Complexes Bridged by a Single 4e Sulfur Ligand: Addition of M'(CO)5 (M' = Cr, Mo, W) to the Ta=S Bond of (t-BuC5H4)2Ta(S)H.
H. Brunner, S. Challet, M. M. Kubicki, J.-C. Leblanc, C. Moïse, F. Volpato, J. Wachter, Organometallics 1995, 14, 3623-3624.
The Reaction of As4Sn (n = 3, 4) and As2S3 with (C5Me4R)2Co2(CO)2 (R = Me, Et): Fragmentation and Reassembling of Main-Group Ligands by Organometallic Complexes.
H. Brunner, H. Kauermann, L. Poll, B. Nuber, J. Wachter, Chem. Ber. 1996, 129, 657-662.
New Insights into the Cage Fragmentation of As4S4 and As4S3 by their Interaction with (C5Me4Et)2Fe2(CO)4.
H. Brunner, L. Poll, J. Wachter, Polyhedron 1996, 15, 573-576.
Addition of Cr(CO)5 to the M(η2-S2) moiety of Cp2M(S2)H (Cp' = tBuC5H4: M = Ta; Cpx = C5Me4Et: M = Nb) and crystal structures of Cp'2TaS2H x [Cr(CO)5]n (n = 1, 2).
H. Brunner, G. Gehart, J.-C. Leblanc, C. Moïse, B. Nuber, B. Stubenhofer, F. Volpato, J. Wachter, J. Organomet. Chem. 1996, 517, 47-51.
Preparation and Reactivity of Peralkylated Tantalocene Sulfur Complexes Having a Fulvenoid Substructure.
H. Brunner, J. Wachter, G. Gehart, J.-C. Leblanc, C. Moïse, Organometallics 1996, 15, 1327-1330.
Synthesis and characterisation of [(C5Me4R)2NbS2]2M complexes (M = Fe, Co; R = Me, Et): organometallic tetrathiometalates with niobocene ligands.
H. Brunner, M. M. Kubicki, G. Gehart, E. Lehrl, D. Lucas, W. Meier, Y. Mugnier, B. Nuber, B. Stubenhofer, J. Wachter, J. Organomet. Chem. 1996, 510, 291-295.
Novel Inorganic Cage Structures Based on AsS Ligands and Cyclopentadienylruthenium Groups.
H. Brunner, B. Nuber, L. Poll, G. Roidl, J. Wachter, Chem. Eur. J. 1997, 3, 57-61.
Koordinative Stabilisierung von cyclo-Tetratellur als [Te4{Cr(CO)5}4]: erstes metallorganisches Derivat eines Tellur-Allotrops.
O. Blacque, H. Brunner, M. M. Kubicki, B. Nuber, B. Stubenhofer, J. Wachter, B. Wrackmeyer, Angew. Chem. 1997, 109, 362-363; Angew. Chem. Int. Ed. Engl. 1997, 36, 352-353.
Gemischte Liganden aus Elementen der 5. und 6. Hauptgruppe: Schnittstelle zwischen Festkörper- und Molekülchemie.
J. Wachter, Angew. Chem. 1998, 110, 782-800; Angew. Chem. Int. Ed. Engl. 1998, 37, 750-768.
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