Serveur d'exploration sur le LRGP

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Eléments de l'association

Column chromatography67
Reaction mixture111
Column chromatography Sauf Reaction mixture" 38
Reaction mixture Sauf Column chromatography" 82
Column chromatography Et Reaction mixture 29
Column chromatography Ou Reaction mixture 149
Corpus5680
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List of bibliographic references

Number of relevant bibliographic references: 29.
Ident.Authors (with country if any)Title
000884 Barry M. Trost [États-Unis] ; W. Michael Seganish ; Cheol K. Chung ; Dominique AmansTotal Synthesis of Laulimalide: Synthesis of the Northern and Southern Fragments
000887 Patricia García-Domínguez ; Rosana Alvarez [Espagne] ; Ángel R. De Lera [Espagne]Survey of Synthetic Approaches to Natural (Peyssonenynes) and Unnatural Acetoxyenediynes
000B48 Vincent Diemer [France] ; Manon Begaud [France] ; Frédéric R. Leroux [France] ; Françoise Colobert [France]Regioselectivity in the Aryne Cross‐Coupling of Aryllithiums with Functionalized 1,2‐Dibromobenzenes
001037 Hilmar Christoph ; Jörg Grunenberg ; Henning Hopf [Allemagne] ; Ina Dix ; Peter Jones [Allemagne] ; Martin Scholtissek [Allemagne] ; Günther Maier [Allemagne]MP2 and DFT Calculations on Circulenes and an Attempt to Prepare the Second Lowest Benzolog, [4]Circulene
001186 Nadia M. Ahmad [Royaume-Uni] ; Vincent Rodeschini [Royaume-Uni] ; Nigel S. Simpkins [Royaume-Uni] ; Simon E. Ward [Royaume-Uni] ; Claire Wilson [Royaume-Uni]Synthetic studies towards garsubellin A: synthesis of model systems and potential mimics by regioselective lithiation of bicyclo[3.3.1]nonane-2,4,9-trione derivatives from catechinic acid
001223 Frédéric Leroux [France] ; Laurence Bonnafoux [France] ; Christophe Heiss [France] ; Françoise Colobert [France] ; Don Antoine Lanfranchi [France]A Practical Transition Metal‐Free Aryl‐Aryl Coupling Method: Arynes as Key Intermediates
001264 Paul Evans [Royaume-Uni] ; Paul Johnson [Royaume-Uni] ; Richard J. K. Taylor [Royaume-Uni]The Epoxy‐Ramberg–Bäcklund Reaction (ERBR): A Sulfone‐Based Method for the Synthesis of Allylic Alcohols
001384 Elena Ioachim ; Elaine A. Medlycott ; Matthew I. J. Polson ; Garry S. Hanan [Canada]Synthesis of a Novel Series of 6,6'‐Disubstituted 4,4'‐Bipyrimidines by Radical Anion Coupling: New π‐Accepting Ligands for Coordination Chemistry
001917 Toshimasa Katagiri [Japon] ; Michiharu Handa [Japon] ; Yasuhisa Matsukawa [Japon] ; J. S. Dileep Kumar [Japon] ; Kenji Uneyama [Japon]Efficient synthesis of an optically pure β-bromo-β,β-difluoroalanine derivative, a general precursor for β,β-difluoroamino acids
001948 Corinne Fruit [France] ; Alain Turck [France] ; Nelly Plé [France] ; Ljubica Mojovic [France] ; Guy Quéguiner [France]A new route to Septorin via controlled metalations of pyrazines. Diazines XXX
001A75 Michael J. Broadhurst [Royaume-Uni] ; Samantha J. Brown [Royaume-Uni] ; Jonathan M. Percy [Royaume-Uni] ; Michael E. Prime [Royaume-Uni]Synthesis of α-hydroxy-β,β-difluoro-γ-ketoesters via [3,3]sigmatropic rearrangements
001B86 Hiroki Kumamoto [Japon] ; Satoru Shindoh [Japon] ; Hiromichi Tanaka [Japon] ; Yoshiharu Itoh [Japon] ; Kazuhiro Haraguchi [Japon] ; Eisen Gen [Japon] ; Atsushi Kittaka [Japon] ; Tadashi Miyasaka [Japon] ; Masato Kondo [Japon] ; Kazuo T. Nakamura [Japon]An Intramolecular Anionic Migration of a Stannyl Group from the 6-Position of 1-(2-Deoxy-d- erythro -pent-1-enofuranosyl)uracil to the 2′-Position: Synthesis of 2′-Substituted 1′,2′-Unsaturated Uridines
001C52 Azhar Ariffin ; Alexander J. Blake ; Mark R. Ebden ; Wan-Sheung Li ; Nigel S. Simpkins ; David N. A. FoxThe diastereoselective and enantioselective substitution reactions of an isoindoline–borane complex
001E95 Olivier Vitse ; Jacques Bompart ; Guy Subra ; Henri Viols ; Roger Escale ; Jean P. Chapat ; Pierre A. Bonnet [France]Aza-indolizine with bridgehead nitrogen. Metalation, halogen-metal exchange and directed ortho -lithiation in the imidazo[1,2- a ]pyrazine series
001F47 Susumu Saito ; Keiko Hatanaka ; Taichi Kano ; Hisashi Yamamoto [Japon]Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6‐Bis(2‐isopropylphenyl)‐3,5‐dimethylphenol as an Extremely Effective Chiral Auxiliary
001F55 H. A. M. Van Mullekom ; J. A. J. M. Vekemans ; E. W. Meijer [Pays-Bas]Band‐Gap Engineering of Donor–Acceptor‐Substituted π‐Conjugated Polymers
002129 Richard A. Ewin ; Angus M. Macleod ; David A. Price ; Nigel S. Simpkins ; Alan P. WattChiral base mediated asymmetric synthesis oftricarbonyl(η6-arene)chromium complexes
002365 Rafael Suau [Espagne] ; Juan Manuel L Pez-Romero [Espagne] ; Rodrigo Rico [Espagne] ; Francisco J. Alonso [Espagne] ; Carolina Lobo [Espagne]A new approach to the synthesis of 4,5-dioxoaporphine alkaloids from preformed biaryl bond precursors
002494 Simonetta A. Fontana [États-Unis] ; Charles R. Davis [États-Unis] ; Charles R. Ya-Bo He [États-Unis] ; Donald J. Burton [États-Unis]The stereoselective preparation of cis and trans -1,2-difluoroethylene synthons
002696 N. Plé [France] ; A. Turck [France] ; K. Couture [France] ; G. Queguiner [France]Metalation of diazines X
002E67 Siegfried E. Drewes ; Craig J. Hogan ; Perry T. Kaye ; Gregory H. P. RoosMedicinal plants of Southern Africa. Part 4. Synthesis of brackenin-like molecules from 1,4-dicarbonyl precursors and by oxidative coupling. X-Ray molecular structure of racemic-2,3-dibenzyl-1,4-diphenylbutane-1,4-dione
002F79 Yuji Naruse [Japon] ; Hisashi Yamamoto [Japon]Asymmetrization of meso-cyclic ketones using homochiral acetal templates
003022 Yoshihiko Ikeda [Japon] ; Junzo Ukai [Japon] ; Nobuo Ikeda [Japon] ; Hisashi Yamamoto [Japon]Selective proton transfer of unsaturated esters
003109 Ben-Ami Feit ; Brigitte Haag ; Jürgen Kast ; Richard R. SchmidtThe effect of an electron-donating β-substituent on the configurational stability and reactivity of vinyl carbanions
003115 Tatsuo Oida ; Shigeo Tanimoto ; Hiromu Terao ; Masaya OkanoRing fragmentations of 2-alkenyl- and 2-benzyl-1,3-dithiolanes induced by bases. A novel method for the preparation of 1,1-bisalkylthio- or 1-alkylthioalk-1-enes and -alka-1,3-dienes
003227 J. W. Streef [Pays-Bas] ; H. C. Van Der Plas [Pays-Bas] ; N. Nieman [Pays-Bas] ; C. H. Stam [Pays-Bas]The reactivity of azepinyl anions, derived from 2‐(diethylamino)‐5‐phenyl‐3H‐azepines, towards alkylating agents
003284 Ben-Ami Feit ; Uri Melamed ; Heike Speer ; Richard R. SchmidtThe configurational stability of vinyl carbanions derived from monosubstituted activated ethylenes
003300 J. W. Streef [Pays-Bas] ; H. C. Van Der Plas [Pays-Bas] ; A. Van Veldhuizen [Pays-Bas] ; K. Goubits [Pays-Bas]The reactivity of the anion of 2‐(diethylamino)‐5‐phenyl‐3H‐azepine. Synthesis of 3‐substituted 2‐(diethylamino)‐5‐phenyl‐3H‐azepines
003409 Ben Ami Feit ; Uri Melamed ; Richard R. Schmidt ; Heike SpeerVinyl anions. Part 9. Vinyl carbanions derived from acrylic esters and their β-phenyl derivatives

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