Serveur d'exploration sur le LRGP - Curation (Istex)

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List of bibliographic references

Number of relevant bibliographic references: 24.
[0-20] [0 - 20][0 - 24][20-23][20-40]
Ident.Authors (with country if any)Title
000019 (2002) O. Dufaud [France] ; E. Favre [France] ; V. Sadtler [France]Porous elastomeric beads from crosslinked emulsions
000035 (1992) F. Pascal [France] ; J. P. Corriou [France] ; C. Dagot [France] ; J. M. Engasser [France] ; B. Daubas [France] ; H. Pingaud [France]Dynamic simulation of an industrial fed-batch alcoholic workshop
000205 (1993) 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
000218 (2001) Toshiyuki Itoh [Japon] ; Kazutoshi Kudo [Japon]Strict base dependence of chirality transfer on [2,3]-Wittig rearrangement of 1,1,2-trifluoroallylic ether
000A74 (1989) D. Roizard [France] ; A. Brembilla [France] ; P. Lochon [France]Design and synthesis of biomimetic polyacrylamides
000B45 (1987) B. Keita [France] ; L. Nadjo [France] ; J. P. Haeussler [France]Activation of electrode surfaces
000B79 (1989) J. C. Andre ; F. Baros ; A. T. Reis E. Sousa [Portugal]Kinetics of partly diffusion‐controlled reaction XXI: A simple algorithm for computing the apparent rate of reaction
000D25 (1996) D. Roizard [France] ; R. Clément [France] ; P. Lochon [France] ; J. Kerres [Allemagne] ; G. Eigenberger [Allemagne]Synthesis, characterization and transport properties of a new siloxane-phosphazene copolymer. Extraction of n -butanol from water by pervaporation
000D55 (1992) Pascal Lorenzini [France] ; Michel Pons [France] ; Jacques Villermaux [France]Free-radical polymerization engineering—IV. Modelling homogeneous polymerization of ethylene: determination of model parameters and final adjustment of kinetic coefficients
000E37 (1993) S. H. Cho [Corée du Sud] ; F. Colin [France] ; M. Sardin [France] ; C. Prost [France]Settling velocity model of activated sludge
001114 (1988) B. Keita [France] ; L. Nadjo [France]Surface modifications with heteropoly and isopoly oxometalates
001115 (1988) B. Keita [France] ; L. Nadjo [France]Surface modifications with heteropoly and isopoly oxometalates
001140 (1999) H. Takeda [Japon] ; K. Shimamura [Japon] ; V. I. Chani [Japon] ; T. Kato [Japon] ; T. Fukuda [Japon]Effect of Starting Melt Composition on Crystal Growth of La3Nb0.5Ga5.5O14
001207 (1994) Danielle Barth [France] ; Dalida Chouchi [France] ; Giovanna Della Porta [Italie] ; Ernesto Reverchon [Italie] ; Michel Perrut [France]Desorption of lemon peel oil by supercritical carbon dioxide: Deterpenation and psoralens elimination
001267 (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
001461 (2000) 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
001482 (1980) P. Le Goff [France]The concept of a ‘unit of degradation of energy’ in fluid flow
001489 (1988) Eric Kvaalen [Israël] ; Daniel Tondeur [France]Constraints on phase equilibrium equations
001495 (1996) 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
001537 (1995) W. A. C. Godoy [Brésil] ; H. G. Fowler [Brésil] ; C. J. Von Zuben [Brésil] ; L. Ziti [Brésil] ; O. B. Ribeiro [Brésil]Larval dispersion in Chrysomya megacephala, Chrysomya putoria and Cochliomyia macellaria (Dipt., Calliphoridae)
001723 (2007) 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

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