Serveur d'exploration sur le LRGP

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Column chromatography And NotReaction mixture

List of bibliographic references

Number of relevant bibliographic references: 38.
Ident.Authors (with country if any)Title
000B65 Vincent Diemer [France] ; Frédéric R. Leroux [France] ; Françoise Colobert [France]Efficient and Complementary Methods Offering Access to Synthetically Valuable 1,2‐Dibromobenzenes
001021 Alexandrine Busch [France] ; Alain Turck [France] ; Nelly Plé [France]Synthesis and molecular design of 4,8‐diaryl‐ and 4,8‐di(arylethynyl)pyrido[4,3‐d]pyrimidines: Potential applications in nonlinear optics. Diazines Part 49
001024 M. Isabel Calaza ; Carlos Cativiela [Espagne]Stereoselective Synthesis of Quaternary Proline Analogues
001266 Jérôme Audoux ; Sylvain Achelle ; Alain Turck ; Francis Marsais ; Nelly Plé [France]Synthesis of new flat polyheterocyclic systems potential DNA intercalating agents diazines part 47
001267 Sylvain Achelle [France] ; Nelly Plé [France] ; Alain Turck [France] ; Jean-Philippe Bouillon [France] ; Charles PortellaSynthesis of aryltrifluoromethylpyridazines application to the synthesis of rod‐like molecules as liquid crystals diazines part 46
001654 Thomas Kaminski ; Philippe Gros ; Yves Fort [France]Side‐Chain Retention During Lithiation of 4‐Picoline and 3,4‐Lutidine: Easy Access to Molecular Diversity in Pyridine Series
001658 Frédéric Toudic [France] ; Alain Turck [France] ; Nelly Plé [France] ; Guy Quéguiner [France] ; Mircea Darabantu [France] ; Thierry Lequeux [France] ; Jean Claude Pommelet [France]Relative ortho‐directing power of fluorine, chlorine and methoxy group for the metalation reaction in the diazine series. Diazines XXXV
001720 Seikou Nakamura [Japon] ; Ikuo Kawasaki [Japon] ; Miki Kunimura [Japon] ; Miyuki Matsui [Japon] ; Yoko Noma [Japon] ; Masayuki Yamashita [Japon] ; Shunsaku Ohta [Japon]Total synthesis of naamine C and pyronaamidine, antitumor marine imidazole alkaloids
001723 Fenton Heirtzlercorrespondence Address Chemical Laboratory School Of Physical Sciences University Of Kent Canterbury Uk Ct2 Nh. E-Mail Frh Ukc. Ac. Uk Fax Tel [Suisse] ; Markus Neuburger [Suisse] ; Klaus Kulike [Suisse]Insights on the synthesis and organisational phenomena of twisted pyrazine–pyridine hybrids
001869 J. A. L Pez-Sastre [Espagne] ; J. D. Mart N-Ramos [Espagne] ; J. F. Rodr Guez-Amo [Espagne] ; M. Santos-Garc A [Espagne] ; M. A. Sanz-Tejedor [Espagne]Stereoselective synthesis of 3-alkylsulfinylmethylisoxazolines and their use as chiral nucleophiles in the chain elongation of 2,3- O -isopropylidene-d-glyceraldehyde
001877 Caroline Muller ; Pascale Even ; Marie-Laure Viriot ; Marie-Christiane CarréProtection and Labelling of Thymidine by a Fluorescent Photolabile Group
001890 Stéphanie Parra [France] ; Olivier Vitse [France] ; Véronique Bénézech [France] ; Carine Deleuze-Masquéfa [France] ; Guy Subra [France] ; Jacques Bompart [France] ; Roger Escale [France] ; Jean P. Chapat [France] ; Pierre A. Bonnet [France]Metalation and halogen‐metal exchange in the imidazo[1,2‐a]quinoxaline series
001B25 V. Gautheron Chapoulaud [France] ; N. Plé [France] ; A. Turck [France] ; G. Quéguiner [France]Synthesis of 4,8-Diarylcinnolines and Quinazolines with Potential Applications in Nonlinear Optics. Diazines. Part 28
001B34 Carlos Cativiela [Espagne] ; Mar A Dolores D Az-De-Villegas [Espagne]Stereoselective synthesis of quaternary α-amino acids. Part 2: Cyclic compounds
001B35 Jan Hein Van Steenis ; Joseph Johannes Gerardus Steven Van Es ; Arne Van Der GenStereoselective Synthesis of (E)‐Vinyl Sulfoxides by the Horner−Wittig Reaction
001B41 Olivier Legrand [France] ; Jean Michel Brunel [France] ; Gérard Buono [France]Scope and Limitations of the Aromatic Anionic [1,3] P–O to P–C Rearrangement in the Synthesis of Chiral o -Hydroxyaryl Diazaphosphonamides
001B43 Yasuhisa Matsukawa [Japon] ; J. S Dileep Kumar [Japon] ; Yuki Yoneyama [Japon] ; Toshimasa Katagiri [Japon] ; Kenji Uneyama [Japon]Reversed diastereoselectivity in the ring-opening reaction of ( S )-TFPO with a chiral aminoacetonitrile Schiff base
001B89 Ana I. Jiménez [Espagne] ; Carlos Cativiela [Espagne] ; Michel Marraud (chimiste) [France]A γ-turn induced by a highly constrained cyclopropane analogue of phenylalanine (c3diPhe) in the solid state
001C80 V. Gautheron Chapoulaud [France] ; I. Salliot [France] ; N. Plé [France] ; A. Turck [France] ; G. Quéguiner [France]Functionalization by metalation of the benzene moiety of benzodiazines. Determination of structures by long-range 1H-15N correlation at natural abundance. Diazines XXV
001E57 Carlos Cativiela [Espagne] ; Mar A Dolores D Az-De-Villegas [Espagne]Stereoselective synthesis of quaternary α-amino acids. Part 1: Acyclic compounds
001E81 Nelly Plé [France] ; Alain Turck [France] ; Arnault Heynderickx [France] ; Guy Quéguiner [France]Functionalization by metallation of fluoropyrazine. Diazines XXI
001E82 Nelly Plé [France] ; Alain Turck [France] ; Arnault Heynderickx [France] ; Guy Quéguiner [France]First metallation of iodo diazines. Iodo and nitrogen directed metallations. Diazines XXII
001F01 Kenji Uneyama [Japon] ; Jian Hao [Japon] ; Hideki Amii [Japon]A novel synthesis of β-trifluoromethyl-substituted isoserine via intramolecular rearrangement of imino ethers
001F07 Otto J. Scherer [Allemagne] ; Sascha Weigel ; Gotthelf Wolmersh User[Cp*Fe(η5‐P5)] as a Useful Source for the Synthesis of Cobalt Complexes with “Naked” Pn Ligands
002098 Nelly Plé [France] ; Alain Turck [France] ; Valérie Chapoulaud [France] ; Guy Quéguiner [France]First functionalization by metallation of the benzene moiety of quinazolines. Diazines XIX
002305 Nobuhiro Sato ; Tomoyuki MatsuuraStudies on pyrazines. Part 32. Synthesis of trisubstituted and tetrasubstituted pyrazines as ant pheromones
002324 Ljubica Mojovic ; Alain Turck ; Nelly Plé ; Muriel Dorsy ; Bruno Ndzi ; Guy Quéguiner [France]Metalation of diazines XVII Very hindered bases as new metalating agents, Improvement of regioselectivity for the metalation of 3-chloro-6-methoxypyridazine
002328 John A. Zoltewicz [États-Unis] ; Carlton D. Dill [États-Unis]Inter-ring directed ortho lithiation by the 2-pyridyl group in bipyridines
002511 Olivier Mongin ; Patrick Rocca ; Laurence Thomas-Dit-Dumont ; François Trécourt ; Francis Marsais ; Alain Godard ; Guy QuéguinerMetallation of pyridine N-oxides and application to synthesis
002512 Keisuke Kato [Japon] ; Hiroyuki Hayakawa [Japon] ; Hiromichi Tanaka [Japon] ; Hiroki Kumamoto [Japon] ; Tadashi Miyasaka [Japon]Lithiation-mediated CC silyl and stannyl migrations observed in 6-chloro-9-(β-d-ribofuranosyl)purine
002564 A. Turck [France] ; N. Pié [France] ; V. Tallon [France] ; G. Quéguiner [France]Metallation of diazines XIV. First O -directed metallation of cinnolines. Metallation of 3-, 4-chloro and 3-, 4-methoxycinnolines
002869 Toshiro Harada ; Tetsuya Yoshida ; Yasuhiro Kagamihara ; Akira OkuResolution and asymmetric synthesis of 3-hydroxycarboxylic acids by using (–)-menthone as a chiral template
002877 Alain Turck [France] ; Nelly Plé [France] ; Bruno Ndzi [France] ; Guy Quéguiner [France] ; Norbert Haider [Autriche] ; Herbert Schuller [Autriche] ; Gottfried Heinisch [Autriche]On the metalation of 3-substituted and 3,6-disubstituted pyridazines
002C36 Mohamed Tabcheh [France] ; Abdelrhani El Achqar [France] ; Louis Pappalardo [France] ; Marie-Louise Roumestant [France] ; Philippe Viallefont [France]Alkylation and protonation of chiral schiff bases: Diastereoselectivity as a function of the nature of reactants
002C58 Tadao Shibutani [Japon] ; Hisashi Fujihara [Japon] ; Naomichi Furukawa [Japon] ; Shigeru Oae [Japon]Ligand exchange reactions of aryl pyridyl sulfoxides with grignard reagents: Convenient preparation of 3‐ and 4‐pyridyl grignard reagents and examination of the leaving abilities of pyridyl anions
002E10 Stephen H. Montgomery [États-Unis] ; Michael C. Pirrung [États-Unis] ; Clayton H. Heathcock [États-Unis]De novo synthesis of carbohydrates by stereoselective aldol reaction: l-cladinose
003111 Hiromichi Tanaka [Japon] ; Hiroyuki Hayakawa [Japon] ; Kikoh Obi [Japon] ; Miyasaka Tadashi [Japon]Synthetic route to 5-substituted uridines via a new type of desulfurizative stannylation
003118 Martin P. Edwards [Royaume-Uni] ; Annette M. Doherty [Royaume-Uni] ; Steven V. Ley [Royaume-Uni] ; Helen M. Organ [Royaume-Uni]Preparation of 2-substituted pyrroles and indoles by regioselective alkylation and deprotection of 1-(2-trimethylsilylethoxymethyl)pyrrole and 1-(2-trimethylsilylethoxymethyl) indole

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