Serveur d'exploration sur le LRGP - Exploration (Accueil)

Index « Teeft.i » - entrée « Methyl group »
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Methyl ether < Methyl group < Methyl groups  Facettes :

List of bibliographic references indexed by Methyl group

Number of relevant bibliographic references: 22.
[0-20] [0 - 20][0 - 22][20-21][20-40]
Ident.Authors (with country if any)Title
000685 (2013) Cuihong Zhang [République populaire de Chine] ; Dongrui Wang [République populaire de Chine] ; Hui Cao [République populaire de Chine, France] ; Ping Song [République populaire de Chine] ; Chaoyong Yang [République populaire de Chine] ; Huai Yang [République populaire de Chine, France] ; Guo-Hua Hu [France, République populaire de Chine]Preparation and electro‐optical properties of polymer dispersed liquid crystal films with relatively low liquid crystal content
000903 (2012) Emily A. Mitchell ; Aldo Peschiulli ; Nicolas Lefevre ; Lieven Meerpoel [Belgique] ; Bert U. W. Maes [Belgique]Direct α‐Functionalization of Saturated Cyclic Amines
000B48 (2011) 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
000B71 (2011) Galina N. Lipunova ; Emiliya V. Nosova ; T V Trashakhova ; Valery N. CharushinAzinylarylethenes: synthesis and photophysical and photochemical properties
001005 (2008) David R. Armstrong [Royaume-Uni] ; Emma Herd [Royaume-Uni] ; David V. Graham [Royaume-Uni] ; Eva Hevia [Royaume-Uni] ; Alan R. Kennedy [Royaume-Uni] ; William Clegg [Royaume-Uni] ; Luca Russo [Royaume-Uni]Synthesis and structural elucidation of solvent-free and solvated lithium dimethyl (HMDS) zincates
001654 (2003) 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
001726 (2002) Philippe Gros ; Yves Fort [France]nBuLi/Lithium Aminoalkoxide Aggregates: New and Promising Lithiating Agents for Pyridine Derivatives
001843 (2001) Alan C. Spivey [Royaume-Uni] ; Adrian Maddaford [Royaume-Uni] ; David P. Leese [Royaume-Uni] ; Alison J. Redgrave [Royaume-Uni]Atropisomeric α-methyl substituted analogues of 4-(dimethylamino)pyridine: synthesis and evaluation as acyl transfer catalysts
001863 (2001) Brian R. Bear [États-Unis] ; Steven M. Sparks [États-Unis] ; Kenneth J. Shea [États-Unis]The Type 2 Intramolecular Diels–Alder Reaction: Synthesis and Chemistry of Bridgehead Alkenes
001944 (2001) Florence Mongin [France] ; Guy Quéguiner [France]Advances in the directed metallation of azines and diazines (pyridines, pyrimidines, pyrazines, pyridazines, quinolines, benzodiazines and carbolines). Part 1: Metallation of pyridines, quinolines and carbolines
001A90 (2000) Yulia V. Smirnova ; Zhanna A. KrasnayaMethods of synthesis of conjugated ω-amino ketones
001B54 (2000) Methods of synthesis of conjugated -amino ketones
001C59 (1999) Mousumi Sannigrahi [Canada]Stereocontrolled synthesis of spirocyclics
001C64 (1999) Alain Petit [France] ; Saad Moulay [Algérie] ; Ta Eb Aouak [Algérie]Polymerization of some terminal alkynes by Ziegler–Natta catalyst systems: Fe(RCOO)3–AlEt3
002694 (1994) Ioannis P. Gerothanassis [Grèce]Multinuclear and multidimensional NMR methodology for studying individual water molecules bound To peptides and proteins in solution: Principles and applications
002932 (1993) The chemistry of acetylcyclopropane
002982 (1993) Abstracts
002A91 (1992) Clayton H. Heathcock [États-Unis]The Enchanting Alkaloids of Yuzuriha
002B91 (1991) Roger V. Bonnert ; Joshua Howarth ; Paul R. Jenkins ; Nicholas J. LawrenceRobinson annulation on a carbohydrate derivative
003018 (1987) M. Watanabe ; E. Shinoda ; Y. Shimizu ; S. Furukawa ; M. Iwao [Japon] ; T. Kuraishi [Japon]Synthesis of bostrycoidin via directed lithiation of tertiary nicotinamide
003227 (1985) 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

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