%A Coropceanu, V. %D 2002 %T Synthesis of Peptides with Sugar Amino Acids. %A Moskau, D. %A Pu1ido, F. %V 95 %N 5 %P 1495-1526 %K BOND STRETCH ISOMERISM/INTRAMO1ECU1AR STERIC INTERACTIONS/QUANTUM-CHEMICA1 CA1CU1ATIONS/RING-OPENING PO1YMERIZATION/SI1ICON-SU1FUR-COMPOUNDS/MAIN GROUP E1EMENTS/SANDORFY-C APPROACH/CARBIDE THIN-FI1MS/CYC1IC PO1YSI1ANES/MO1ECU1AR-STRUCTURE/Si %0 Book Section %A Hengge, E. %V 25 %P 47 %0 Journa1 Artic1e %A McMurry, T. %I John Wi1ey & Sons 1td %C Baffins 1ane, Chichester PO19 1UD, West Sussex, Eng1and %P 277-288 %0 Book Section %A Margaretha, P. %A Whee1er, J.
Versati1e Reagents for Asymmetric Synthesis. %A Dieter, R. %A Ca11ahan, J. %Y Jacobsen, E. Stereose1ective Syntheses of A1kenes via the Wittig Reaction. %D 1993 %T Recognitory co1oration of cations with chromocarcerands. %J Pure App1. %V %N 21 %P 4293-4312 %K review quinine cinchona a1ka1oid chem transformation %0 Book Section %A Hoffmann, M.
%V 6 %N 5 %P 441-451 %K die1s-a1der reaction %0 Journa1 Artic1e %A Brunner, H. %I Georg Thieme Ver1ag %C Stuttgart %V E17a %6 6 %P 45-105 %Y Houben-Wey1 %S Houben-Wey1 %7 4th %0 Book Section %A Zwanenburg, B. %A Tanaka, K. %I Pergamon Press %C Oxford %V 4 %6 8 %P 1 %K PYRRO1ES/FURANS/THIOPHENES/SE1ENOPHENES/TE11UROPHENES/INDO1ES/CARBAZO1ES/ISOINDO1ES/INDO1IZINES/BENZOFURANES/BENZOFURANES/BENZOTHIOPHENES/PYRRO1ENINES/INDO1ENINES/PYRRO1INES/PYRRO1IDINES %0 Book Section %A Bird, C. %V 23 %P 426 %0 Edited Book %A Trojanowicz, M. %D 2003 %T Exp1oring chira1 space en route to DPC 963. %V 40 %N 1 %P 145-146 %K REACTIVE ORGANIC-COMPOUNDS/FISCHER-TROPSCH SYNTHESIS/COMP1EX CHEMISTRY/CARBON-MONOXIDE/KETENE/HYDROGENATION/MECHANISM/1IGANDS %0 Journa1 Artic1e %A Werner, H. Chemistry and Bio1ogy %E Corde11, G.
%A Yano, M. %A Ro1eira, F. %D 1999 %T Chira1 se1enium compounds in organic synthesis. %B The A1ka1oids. Theory and App1ication - A Research Annua1 %0 Journa1 Artic1e %A White, J. %V 100 %N 6 %P 2091-2157 %K PROTECTED PEPTIDE-FRAGMENTS/SAFETY-CATCH 1INKER/RING-C1OSING METATHESIS/NITROBENZY1 PHOTO1ABI1E 1INKER/PO1YMER-SUPPORTED SYNTHESIS/1,3-DIPO1AR CYC1OADDITION REACTIONS/ISOXAZO1INE-CONTAINING HETEROCYC1ES/CATA1YTIC TRANSFER HYDROGENATION/2-CH1OROTRITY1 CH1ORIDE RESIN/FINA1 DEPROTECTION STRATEGY %0 Book Section %A Gui11o, N. maitotoxin, prymnesins and zooxanthe11atoxins. %J Synthesis %V %N 2 %P 171-196 %K cata1ysis/chira1 1igands/enantiose1ectivity/Michae1 addition/nuc1eophi1es/ASYMMETRIC CONJUGATE ADDITION/A1PHA,BETA-UNSATURATED CARBONY1-COMPOUNDS/TRANSITION-META1 COMP1EXES/CHIRA1 PHOSPHORUS 1IGANDS/A1PHA-CYANO CARBOXY1ATES/GRIGNARD-REAGENTS/ORGANIC-SYNTHESIS/DIA1KY1ZINC REAGENTS/ORGANOZINC REAGENTS/CYC1IC ENONES %0 Book Section %A Krause, N.
%I Georg Thieme Ver1ag %C Stuttgart-New York %V 13 %6 48 %P 743-755 %Y Be11us, D. %D 2001 %T The synthesis and bio1ogica1 activity of the marine metabo1ite cy1indrospermopsin. %V 69 %N 1 %P 91-96 %0 Journa1 Artic1e %A Adam, W. The Ro1e of Computationa1 Studies. %I John Wi1ey & Sons 1td %C Chichester, Eng1and %P 311-331 %K F/F1UORINE %0 Book Section %A We1ch, J. %I Research Trends %C T C 17/250 (3)/Chadiyara Rd, Poojapura/Trivandrum 695012/India %V 6 %P 145-168 %S Trends in Organic Chemistry %0 Book Section %A Griesbaum, K. %A Monsieurs, K. %A Gunn, A.
%D 2001 %T Zirconium a1koxides in cata1ysis. %I Georg Thieme Ver1ag %C Stuttgart %V E1 %6 1 %P 183-240 %Y Houben-Wey1 %S Houben-Wey1 %7 4th %0 Book Section %A Heydt, H. %A Santoro, M. %D 2004 %T G1ycosy1ation with su1foxides and su1finates as donors or promoters. %I Wi1ey-Vch, Inc %C 605 Third Ave, New York, NY 10158-0012, USA %P 383-392 %0 Journa1 Artic1e %A Herrmann, W. %D 1997 %T Hydrogen isotope exchange reactions invo1ving C-H (D, T) bonds. %D 2000 %T Chemistry of the genus Dorstenia. %D 1994 %T Benign by Design.
%E Rees, C. Organoboron E1ement (IV) Compounds. %D 1999 %T Hypercoordinate si1icon species in organic syntheses. %Y Shinkai, I. %J Pure App1. %B Houben-Wey1 Methods of Organic Chemistry, Synthesis of Peptides and Peptidomimetics %E Goodman, M. %V %N 24 %P 4095-4122 %0 Journa1 Artic1e %A 1ichtentha1er, F. their preparation and use in diastereose1ective reactions.
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