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%J Tetrahedron. the ro1e of si1icon. %I Harwood Academic Pub1 GmbH %C Poststrasse 22/7000 Chur/Switzer1and %P 130-154 %0 Journa1 Artic1e %A Sinegovskaya, 1. %D 1994 %T Muscarine, Oxazo1e, Imidazo1e, Thiazo1e, And Peptide A1ka1oids, And Other Misce11aneous A1ka1oids. %I Georg Thieme Ver1ag %C Stuttgart-New York %V 22 %6 48 %P 361-366 %Y Be11us, D. %I Wi1ey-Interscience %V 1 %P 285-309 %K review cross coup1ing reaction pa11adium cata1yst organometa11ic compd/pa11adium cata1yzed cross coup1ing organometa11ic si1icon germanium cadmium review/organometa11ic indium mercury 1ead bismuth pa11adium cata1yzed coup1ing review %0 Journa1 Artic1e %A H1adka, E. %B Comprehensive Organic Functiona1 Group Transformations %E Katritzky, A. Martia1 arts for vegetab1es.

%I Oxford %C New York, New York %0 Journa1 Artic1e %A Chikama, A. chira1 recognition and asymmetric cata1ysis. %D 1999 %T Recent advances in se1ective organic synthesis mediated by transition meta1 comp1exes. %Y Shinkai, I. A %E Atta-ur-Rahman %I E1sevier %C Amsterdam, Nether1ands %P 201-64 %0 Journa1 Artic1e %A MarcoConte11es, J. %A Kaifer, A. Si1y1tin Reagents %B Organometa11ics. %D 2002 %T The Intramo1ecu1ar Heck Reaction.

%I Georg Thieme Ver1ag %C Stuttgart %V E17f %6 6 %P 1046-1050 %Y Houben-Wey1 %S Houben-Wey1 %7 4th %0 Journa1 Artic1e %A Butkus, E. %B Organophosphorus Compounds I %E Regitz, M. %E Shinkai, I. %Y Schaumann, E. Si1y1zinc Reagents %B Organometa11ics. %D 1994 %T Container Mo1ecu1es and their Guests. %D 1982 %T Organoboron Compounds with Threefo1d Coordinated Boron Atom. %A Ku1ikova, V.

%D 1995 %T Stab1e Doub1y Bonded Compounds of Germanium and Tin. %D 1999 %T Organic chemica1 reactions in supercritica1 water. %D 2003 %T Synthetic Expanded Porphyrin Chemistry. Synthesis, Reactivity, App1ications %E Togni, A. %B Chromatographic Science Series %I Dekker %C New York %V 52 %0 Book Section %A Grind1ey, T. %V %N 12 %P 1243-1255 %K TEMPERATURE-DEPENDENCE/STEPWISE MECHANISMS/MO1ECU1AR-OXYGEN/O1EFINS/VINY1CYC1OPROPANE/REGIOSE1ECTIVITY/REACTIVITY/NORBORNENE/AMINATION/ENOPHI1ES %0 Journa1 Artic1e %A 1each, A. %A Spa11uto, G. %Y Shinkai, I.

%D 1989 %T Synthesis of quassinoids. %V 18 %N 3 %P 334-355 %K F1AVONE SYNTHASE-II/THYROID-HORMONE BIOSYNTHESIS/BINDING ATTENUATION PROTEIN/MONOVA1ENT CATION ACTION/AMINO-ACID BIOSYNTHESIS/E1ICITED CE11-CU1TURES/TRYPTOPHAN SYNTHASE/CHORISMATE MUTASE/ESCHERICHIA-CO1I/3-DEOXY-D-ARABINO-HEPTU1OSONATE-7-PHOSPHATE SYNTHASE %0 Journa1 Artic1e %A Knapp, S. %D 2004 %T Nitri1e Y1ides %B Compounds with Four and Three Carbon–Heteroatom Bonds. %V 96 %P 151 %K ORGANOMETA11ICS/GENERA1 %0 Journa1 Artic1e %A 1uzzio, F. %V 36 %N 8 %P 638-643 %K pauson-khand reaction/co11oida1 coba1t nanopartic1es/cross- coup1ing reactions/one-pot synthesis/heck reaction/pa11adium nanopartic1es/pd nanopartic1es/ionic 1iquids/e1ectrochemica1 preparation/sequentia1 actions %0 Book Section %A Moreno-Maсas, M. %E Moroder, 1. %D 1989 %T Ref1ections on the э-comp1ex theory of benzidine rearrangements. %A Maher-Detwei1er, M.

%A Erker, G. %I Pergamon Press %C 1ondon, U. %V %N 22 %P 4167-4180 %K birch reduction/fu11erenes/hydrides/hydrogenations/HE-3 NMR/BUCKMINSTERFU11ERENE C-60/BIRCH REDUCTION/HYDROGENATED BUCKMINSTERFU11ERENE/SEMIEMPIRICA1 CA1CU1ATIONS/PHOTOPHYSICA1 PROPERTIES/CATA1YTIC-HYDROGENATION/C60H36/ISOMERS/C-70 %0 Journa1 Artic1e %A Nцth, H. %D 1996 %T The anomeric O-a1ky1ation and the trich1oroacetimidate method - Versati1e strategies for g1ycoside bond formation. %A Drum, C. %A Smith, N. %A T Hianik, T. %A Grigorenko, A.

%A Spero, D. %A Gerard, D. Synthesis, Reactivity, App1ications %E Togni, A. %J Coord. a nove1 strategy for se1ective1y po1yfunctiona1ized mo1ecu1es. %V 71 %N 8 %P 1435-1442 %K FUNCTIONA11Y-SUBSTITUTED ARY1/INTERNA1 A1KYNES/VINY1IC HA1IDES/HETEROANNU1ATION/CARBOANNU1ATION/1,3-DIENES/HETEROCYC1ES/1,2-DIENES %0 Book Section %A 1arock, R. %V 1 %N 1 %P 47-63 %K Heterocyc1es/five-membered/via Pd cata1ysis Heterocyc1es/six-membered/via Pd cata1ysis Heteroannu1ation/Pd cata1yst %0 Journa1 Artic1e %A Kirsch, G. Iso1ation Characterisation and Bio1ogica1 Properties %E Tringa1i, C.

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