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Authors: PEERLINGS HWI NEPOGODIEV SA STODDART JF MEIJER EW
Citation: Hwi. Peerlings et al., SYNTHESIS OF SPACER-ARMED GLUCODENDRIMERS BASED ON THE MODIFICATION OF POLY(PROPYLENE IMINE) DENDRIMERS, EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, (9), 1998, pp. 1879-1886

Authors: PEERLINGS HWI MEIJER EW
Citation: Hwi. Peerlings et Ew. Meijer, SYNTHESIS AND CHARACTERIZATION OF AXIALLY CHIRAL MOLECULES CONTAININGDENDRITIC SUBSTITUENTS, EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, (4), 1998, pp. 573-577

Authors: PEERLINGS HWI TRIMBACH DC MEIJER EW
Citation: Hwi. Peerlings et al., CHIRAL DENDRIMERS WITH BACKFOLDING WEDGES, Chemical communications, (4), 1998, pp. 497-498

Authors: PEERLINGS HWI STRUIJK MP MEIJER EW
Citation: Hwi. Peerlings et al., CHIRAL OBJECTS WITH A DENDRITIC ARCHITECTURE, Chirality, 10(1-2), 1998, pp. 46-52

Authors: ASHTON PR BOYD SE BROWN CL NEPOGODIEV SA MEIJER EW PEERLINGS HWI STODDART JF
Citation: Pr. Ashton et al., SYNTHESIS OF GLYCODENDRIMERS BY MODIFICATION OF POLY(PROPYLENE IMINE)DENDRIMERS, Chemistry, 3(6), 1997, pp. 974-984

Authors: PEERLINGS HWI MEIJER EW
Citation: Hwi. Peerlings et Ew. Meijer, CHIRALITY IN DENDRITIC ARCHITECTURES, Chemistry, 3(10), 1997, pp. 1563-1570

Authors: VANHAARE JAEH GROENENDAAL L PEERLINGS HWI HAVINGA EE VEKEMANS JAJM JANSSEN RAJ MEIJER EW
Citation: Jaeh. Vanhaare et al., UNUSUAL REDOX BEHAVIOR OF ALPHA-OLIGOHETEROAROMATIC COMPOUNDS - AN INCREASING FIRST OXIDATION POTENTIAL WITH INCREASING CONJUGATION LENGTH, Chemistry of materials, 7(10), 1995, pp. 1984-1989

Authors: JANSEN JFGA PEERLINGS HWI DEBRABANDERVANDENBERG EMM MEIJER EW
Citation: Jfga. Jansen et al., OPTICAL-ACTIVITY OF CHIRAL DENDRITIC SURFACES, Angewandte Chemie, International Edition in English, 34(11), 1995, pp. 1206-1209

Authors: GROENENDAAL L PEERLINGS HWI HAVINGA EE VEKEMANS JAJM MEIJER EW
Citation: L. Groenendaal et al., OLIGOHETEROCYCLES BY THE STILLE-COUPLING REACTION, Synthetic metals, 69(1-3), 1995, pp. 467-470

Authors: GROENENDAAL L PEERLINGS HWI VANDONGEN JLJ HAVINGA EE VEKEMANS JAJM MEIJER EW
Citation: L. Groenendaal et al., WELL-DEFINED OLIGO(PYRROLE-2,5-DIYL)S BY THE ULLMANN REACTION, Macromolecules, 28(1), 1995, pp. 116-123
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