Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' SEMPLE JE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 26 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Owens, TD; Semple, JE
      Atom-economical synthesis of the N(10)-C(17) fragment of cyclotheonamides via a novel passerini reaction-deprotection-acyl migration strategy

      ORGANIC LETTERS
    2. Owens, TD; Araldi, GL; Nutt, RF; Semple, JE
      Concise total synthesis of the prolyl endopeptidase inhibitor eurystatin Avia a novel Passerini reaction-deprotection-acyl migration strategy

      TETRAHEDRON LETTERS
    3. Semple, JE; Owens, TD; Nguyen, K; Levy, OE
      New synthetic technology for efficient construction of alpha-hydroxy-beta-amino amides via the Passerini reaction

      ORGANIC LETTERS
    4. Siev, DV; Semple, JE
      Novel Hydrazino-Carbonyl-Amino-Methylated polystyrene (HCAM) resin methodology for the synthesis of P-1-aldehyde protease inhibitor candidates

      ORGANIC LETTERS
    5. Tamura, SY; Levy, OE; Uong, TH; Reiner, JE; Goldman, EA; Ho, JZ; Cohen, CR; Bergum, PW; Nutt, RF; Brunck, TK; Semple, JE
      Guanylpiperidine peptidomimetics: Potent and selective bis-cation inhibitors of factor Xa

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    6. Semple, JE; Levy, OE; Minami, NK; Owens, TD; Siev, DV
      Novel, potent and selective chimeric FXa inhibitors featuring hydrophobic P-1-ketoamide moieties

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    7. Reiner, JE; Lim-Wilby, MS; Brunck, TK; Ha-Uong, T; Goldman, EA; Abelman, MA; Nutt, RF; Semple, JE; Tamura, SY
      Investigation of the S-3 site of thrombin: Design, synthesis and biological activity of 4-substituted 3-amino-2-pyridones incorporating P-1-argininals

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    8. Ho, JZ; Levy, OE; Gibson, TS; Nguyen, K; Semple, JE
      Exploratory solid-phase synthesis of factor Xa inhibitors: Discovery and application of P-3-heterocyclic amides as novel types of non-basic arginine surrogates

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    9. Tamura, SY; Goldman, EA; Bergum, PW; Semple, JE
      Novel benzo-fused lactam scaffolds as factor Xa inhibitors

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    10. Minami, NK; Reiner, JE; Semple, JE
      Asymmetric synthesis of novel quaternary alpha-hydroxy-delta-lactam dipeptide surrogates

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    11. Siev, DV; Gaudette, JA; Semple, JE
      Novel protocol for the solid-phase synthesis of peptidyl and peptidomimetic P-1-argininal derivatives

      TETRAHEDRON LETTERS
    12. SEMPLE JE
      DESIGN AND CONSTRUCTION OF NOVEL THROMBIN INHIBITORS FEATURING P-3-P-4 QUATERNARY LACTAM DIPEPTIDE SURROGATES

      Bioorganic & medicinal chemistry letters
    13. Semple, JE; Rowley, DC; Owens, TD; Minami, NK; Uong, TH; Brunck, TK
      Potent and selective thrombin inhibitors featuring hydrophobic, basic P-3-P-4-aminoalkyllactam moieties

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    14. Owens, TD; Semple, JE
      Alkoxide-catalyzed ring-opening of a novel homosaccharin derivative: Synthesis of potent, selective P-3-lactam thrombin inhibitors containing P-4-o-alkoxycarbonylbenzylsulfonamide residues'

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    15. SEMPLE JE
      EFFICIENT CONSTRUCTION OF NOVEL QUATERNARY LACTAM DIPEPTIDE SURROGATES

      Tetrahedron letters
    16. ROTHERHAM LW; SEMPLE JE
      A PRACTICAL AND EFFICIENT SYNTHETIC ROUTE TO DIHYDROPIPERCIDE AND PIPERCIDE

      Journal of organic chemistry
    17. KRISHNAN R; ZHANG E; HAKANSSON K; ARNI RK; TULINSKY A; LIMWILBY MSL; LEVY OE; SEMPLE JE; BRUNCK TK
      HIGHLY SELECTIVE MECHANISM-BASED THROMBIN INHIBITORS - STRUCTURES OF THROMBIN AND TRYPSIN INHIBITED WITH RIGID PEPTIDYL ALDEHYDES

      Biochemistry
    18. SEMPLE JE; ROWLEY DC; BRUNCK TK; RIPKA WC
      SYNTHESIS AND BIOLOGICAL-ACTIVITY OF P-2-P-4 AZAPEPTIDOMIMETIC P-1-ARGININAL AND P-1-KETOARGININAMIDE DERIVATIVES - A NOVEL CLASS OF SERINE-PROTEASE INHIBITORS

      Bioorganic & medicinal chemistry letters
    19. TAMURA SY; GOLDMAN EA; BRUNCK TK; RIPKA WC; SEMPLE JE
      RATIONAL DESIGN, SYNTHESIS, AND SERINE-PROTEASE INHIBITORY ACTIVITY OF A NOVEL P-1-ARGININAL DERIVATIVE FEATURING A CONFORMATIONALLY CONSTRAINED P-2-P-3-BICYCLIC LACTAM MOIETY

      Bioorganic & medicinal chemistry letters
    20. SEMPLE JE; MINAMI NK; TAMURA SY; BRUNCK TK; NUTT RF; RIPKA WC
      RATIONAL DESIGN AND SYNTHESIS OF A NOVEL, SELECTIVE CLASS OF THROMBININHIBITORS - P-1-ARGININAL DERIVATIVES INCORPORATING P-3-P-4 QUATERNARY LACTAM DIPEPTIDE SURROGATES

      Bioorganic & medicinal chemistry letters
    21. TAMURA SY; SEMPLE JE; REINER JE; GOLDMAN EA; BRUNCK TK; LIMWILBY MS; CARPENTER SH; ROTE WE; OLDESHULTE GL; RICHARD BM; NUTT RF; RIPKA WC
      DESIGN AND SYNTHESIS OF A NOVEL CLASS OF THROMBIN INHIBITORS INCORPORATING HETEROCYCLIC DIPEPTIDE SURROGATES

      Bioorganic & medicinal chemistry letters
    22. MURRAY WM; SEMPLE JE
      FACILE ACCESS TO NOVEL 1,4-DIHYDROXYNAPHTHALENE-2,3-DICARBOXIMIDES AND HETEROFUSED ANALOGS

      Synthesis
    23. SEMPLE JE; RYDZEWSKI RM; GARDNER G
      AN EFFICIENT SYNTHETIC ROUTE TO ETHYL YDROXY-1,3(2H,4H)-DIOXOISOQUINOLINE-4-CARBOXYLATES

      Journal of organic chemistry
    24. LEVY OE; SEMPLE JE; LIM ML; REINER J; ROTE WE; DEMPSEY E; RICHARD BM; ZHANG E; TULINSKY A; RIPKA WC; NUTT RF
      POTENT AND SELECTIVE THROMBIN INHIBITORS INCORPORATING THE CONSTRAINED ARGININE MIMIC L-3-PIPERIDYL(N-GUANIDINO)ALANINE AT P-1

      Journal of medicinal chemistry
    25. SEMPLE JE; ROWLEY DC; BRUNCK TK; HAUONG T; MINAMI NK; OWENS TD; TAMURA SY; GOLDMAN EA; SIEV DV; ARDECKY RJ; CARPENTER SH; GE Y; RICHARD BM; NOLAN TG; HAKANSON K; TULINSKY A; NUTT RF; RIPKA WC
      DESIGN, SYNTHESIS, AND EVOLUTION OF A NOVEL, SELECTIVE, AND ORALLY BIOAVAILABLE CLASS OF THROMBIN INHIBITORS - P1-ARGININAL DERIVATIVES INCORPORATING P3-P4 LACTAM SULFONAMIDE MOIETIES

      Journal of medicinal chemistry
    26. SEMPLE JE
      A CONCISE SYNTHESIS OF PELLITORINE

      Organic preparations and procedures international


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/01/21 alle ore 04:20:15