Index Name

Kelly, Stephen

Similar Names

Kelly, S.;   Kelly, Stephen M.

Co-authors

Bault, Philip;   Boller, Arthur;   Buchecker, Richard;   Fromm, Hans-Jürgen;   Germann, Alfred;   Gode, Paul;   Godé, Paul;   Goethals, Gerard;   Goethals, Gérard;   Goodby, John;   Haley, Julie;   Harmouch, Benali;   Leenhouts, Frans;   Letellier, Philippe;   Lukac, Teodor;   Mackenzie, Grahame;   Martin, Patrick;   Mehl, Georg;   Rolf, Peter;   Ronco, Gino;   Schadt, Martin;   Schmitt, Klaus;   Schuster, Andreas;   Villa, Pierre;   Villiger, Alois;   Watson, Marcus

Publication Titles

1987: Liquid-crystal derivatives of phenyl benzoate for electrooptical display devices
1987: Liquid-crystal pyridine derivatives for electrooptical display devices
1988: Ferroelectric liquid crystals
1989: Cyclohexyl esters of .alpha.-fluorocarboxylic acids, their preparation, liquid-crystal mixtures containing them, and their use for electrooptical purposes
1989: Liquid crystal components with a trimethylenoxy group
1989: Optically active liquid-crystal compounds and mixtures and electrooptical cells containing them
1990: Compounds having trans-3-cyclohexylallyloxy groups and liquid-crystal mixtures and electrooptical devices using them
1991: (4-Arylbutyl)cyclohexane derivatives for liquid crystal compositions for electrooptical display devices
1991: Optically active compounds for liquid crystal mixtures for electrooptical display devices
1991: Preparation of (4E-cyclohexyl-3-butenyl)phenyl derivatives as liquid crystal components
1991: Preparation of optically active naphthalene-2,6-dicarboxylate esters as dopants for liquid crystals
1992: Preparation of 3-(4-phenylcyclohexyl)-2-propenyl ethers and analogs as liquid crystal components
1993: Chiral oxazolines as dopants for liquid crystal mixtures, the mixtures, and their use
1993: Fatty acid esters containing a pyridine or pyrimidine ring and their use as components of liquid crystal mixtures and for electrooptical applications
1993: Optically active chiral piperazine derivatives, liquid crystal mixtures containing them, and the use of the mixtures for optical and electrooptical applications
1994: Cyclohexyl alkenoates as components for liquid crystalline mixtures
1994: Orientation layers for liquid crystals
1995: Photocurable liquid crystals and their use in optical devices
1996: Optically active photocurable smectic liquid crystals and their use in optical devices
1996: Photo cross-linkable liquid crystals
1996: Photocrosslinkable liquid-crystalline dyes and their use
1996: Photopolymerizable liquid crystals, liquid-crystal mixtures containing them, and their use in the cured state for optical or electronic devices
1996: Preparation of phenyl 4-[(E)-alk-2-enoyloxy]benzoates as liquid crystal components
1996: Preparation of photocrosslinkable naphthalene derivatives for liquid crystals
1997: Liquid crystals from derivatives from alkoxyalkoxy substituted nitrogen containing hetero rings for electrooptical devices
1997: Manufacture of photocrosslinkable, liquid crystalline 1,4-dioxane-2,3-diyl derivatives
1997: Photocrosslinkable chiral doping agents
1997: Photocrosslinkable liquid crystalline 1,2-phenylene derivatives and their use in optical devices
1997: Synthesis of O-alkyl D-xylitols with potential liquid-crystalline properties
1999: Synthesis and mesomorphism of four series of 6-Z-n-alkyl-α-D-galactopyranoses

Sources

EP 242.716 (1987/10/28)
EP 247.466 (1987/12/02)
EP 268.198 (1988/05/25)
EP 269.963 (1988/06/08)
EP 304.738 (1989/03/01)
EP 343.487 (1989/11/29)
EP 344.557 (1989/12/06)
EP 393.501 (1990/10/24)
EP 410.233 (1991/01/30)
EP 415.220 (1991/03/06)
EP 442.306 (1991/08/21)
EP 449.049 (1991/10/02)
EP 471.287 (1992/02/19)
EP 523.543 (1993/01/20)
EP 534.258 (1993/03/31)
EP 546.298 (1993/06/16)
EP 595.144 (1994/05/04)
EP 611.786 (1994/08/24)
EP 675.186 (1995/10/04)
EP 690.047 (1996/01/03)
EP 699.731 (1996/03/06)
EP 700.981 (1996/03/13)
EP 731.084 (1996/09/11)
EP 748.852 (1996/12/18)
EP 754.685 (1997/01/22)
EP 755.915 (1997/01/29)
EP 755.918 (1997/01/29)
EP 755.929 (1997/01/29)
J. Carbohydr. Chem., 16, 479
Mol. Cryst. Liq. Cryst. A, 332, 391
US 5.567.349 (1996/10/22)


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