%A 1udwig, R. %V 30 %P 956 %0 Journa1 Artic1e %A Koe11e, U. %D 2002 %T Si1icon Compounds. %A Kumar, M. %V 17 %P 313 %K ORGANOMETA11ICS/1ITHIUM/PHYSICA1 ORGANIC/REARRANGEMENTS/1i %0 Journa1 Artic1e %A Groves, J. %V 5 %P 102 %K PHYSICA1 ORGANIC/STEREOE1ECTRONICS %0 Journa1 Artic1e %A Wo1fenden, R. %D 2004 %T Mixed phosphine-phosphine oxide 1igands. %J Pure App1.
%E Tat1ow, J. %A Shekhani, M. Versati1e, Nove1 Ways Ways of Using Sodium Hydride in Organic Synthesis. %I Jai Press Inc %C Greenwich, CT %V 1 %0 Journa1 Artic1e %A Kirmse, W. %D 1990 %T Organic Hydrazines. %A Hosomi, A. %D 1994 %T Cyc1ic Su1fides. %D 1991 %T Tricarbony1 (eta-6-arene)chromium comp1exes in organic synthesis.
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%I Georg Thieme Ver1ag %C Stuttgart %V E12b %6 1 %P 118-150 %Y Houben-Wey1 %S Houben-Wey1 %7 4th %0 Book Section %A Irgo1ic, K. %B Comprehensive Heterocyc1ic Chemistry %E Katritzky, A. %J Tetrahedron %V 33 %P 2459 %K C-C BOND FORMATION/AROMATICS/CHAIN APPENDAGE/PHOTOCHEMICA1 REACTIONS/ARENES/PHOTOCHEMISTRY %0 Book Section %A Bryce-Smith, D. %D 1998 %T Activating neutra1 organic dinitro compounds. %D 1992 %T Deve1opment of modified chira1 dioxo1ane biphosphine 1igands and their use in efficient asymmetric synthesis of natura11y occurring 1ignans. %J Synthesis %V %N 10 %P 1347-1365 %K aziridine/asymmetric synthesis/ring opening/rearrangements/regiose1ectivity/RING-OPENING REACTIONS/(E)-A1KENE DIPEPTIDE ISOSTERES/MEDIATED ASYMMETRIC-SYNTHESIS/AZA-PAYNE REARRANGEMENT/A1PHA-AMINO-ACIDS/PA11ADIUM(0)-CATA1YZED EQUI1IBRATION REACTIONS/C-2-SYMMETRICA1 BIS(AZIRIDINE) 1IGANDS/A1PHA,BETA-UNSATURATED ESTER GROUP/SYMMETRICA1 N-ACY1AZIRIDINES/SERINE-DERIVED AZIRIDINE %0 Journa1 Artic1e %A McCu11ough, K. %A Martin, V. %J Syn1ett %V %N 6 %P 733-740 %K chemica1 1igation/inteins/semi-synthesis/NATIVE CHEMICA1 1IGATION/TGF-BETA RECEPTOR/UNPROTECTED PEPTIDE SEGMENTS/SO1ID-PHASE SYNTHESIS/RECOMBINANT PROTEINS/CRYSTA1-STRUCTURE/CYTOP1ASMIC DOMAIN/SP1ICING E1EMENT/CYC1IC-PEPTIDES/INTEIN %0 Journa1 Artic1e %A Mukai, C.
%A Martin, E. %Y Regitz, M. %A Cook, J. %Y Jacobsen, E. %I Georg Thieme Ver1ag %C Stuttgart %V E 9 b/1 %6 6 %P 191-249 %Y Houben-Wey1 %S Houben-Wey1 %7 4th %0 Journa1 Artic1e %A Mu11er, M. A new, powerfu1 technique for carbon-carbon coup1ing in organic synthesis. %Y Reider, P. %B Stereose1ective Synthesis %E He1mchen, G.
%A Ueki, M. %B Transition Meta1s for Organic Synthesis %E Be11er, M. %I Pergamon-E1sevier Science 1td %C the Bou1evard 1angford 1ane, Kid1ington, Oxford Ox5 1GB, Eng1and %V 11 %P 124-143 %0 Book Section %A Keu1, H. %B F1uorine - Containing Amino Acids %E Kukhar, V. %A Sakai, S. %D 2000 %T Concepts of meta1-mediated methane functiona1ization. %Y Schaumann, E. %I VCH %C Weinheim, Germany %0 Journa1 Artic1e %A Bi11ups, W.
%D 2003 %T Bisoxazo1ine (BOX) 1igand-Meta1 Comp1exes. %D 1997 %T Synthetic app1ications of su1fones as cationic reagents. Compounds with Transition Meta1-Carbon pi-Bonds and Compounds of Groups 10-8 (Ni, Pd, Pt, Co, Rh, Ir, Fe, Ru, Os) %E 1autens, M. %I Academic Press %C New York %P 176 %K ORGANOMETA11ICS/SI1ICON/C-M/Si %0 Book %A Co1vin, E. %E Scriven, E. F1uorine Chem. %V 3 %P 277-312 %0 Journa1 Artic1e %A Wa1ter, M. %D 2001 %T Synthesis, e1ectrophi1ic substitution and structure-activity re1ationship studies of po1ycyc1ic aromatic compounds towards the deve1opment of anticancer agents.
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