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Thomas, E. Synthesis and platelet aggregation inhibitory activity of 4,5-bis substituted -1,2,3-thiadiazoles. Jagtap, S. Heck reaction-State of the Art. Catalysts , , 7 , Kondo, Y. Photoinduced cyclorelease for condensed heteroaromatic synthesis. McCormick, J. DeVita, R. Rowley, M.

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Sherlock, M. Solid phase combinatorial synthesis of 4-hydroxyquinolin-2 1H -ones.

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  6. Liu, Y. Solid phase synthesis of 3- 5-arylpyridinyl hydroxycoumarins.

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    Hong, B. Traceless Solid phase synthesis of heterosteroid framework. Szardenings, A. A simple procedure for the solid phase synthesis of diketopiperazine and diketomorpholine derivatives. Tetrahedron , , 53 , Gordon, D. Reductive alkylation on a solid phase: Synthesis of a piperazinedione combinatorial library. Iyer, M. Asymmetric catalysis of the strecker amino acid synthesis by a cyclic dipeptide.

    Kowalski, J. Solid phase synthesis of a diketopiperazine catalyst containing the unnatural amino acid S -Norarginine. Mhaske, S. The chemistry of recently isolated naturally occurring quinazolinone alkaloids. Tetrahedron , , 62 , Smith, A. An efficient solid phase synthetic route to 1,3-disubstituted 2,4 1H,3H -quinazolinediones suitable for combinatorial synthesis.

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    Introduction to Chemical Biology 128. Lecture 04. Combinatorial Chemistry and Biology.

    Wang, H. Total synthesis of the fumiquinazoline alkaloids: Solid phase studies. Tiwari, V. Carbohydrate-based potential chemotherapeutic agents: Recent developments and their scope in future drug discovery.

    Carbohydrate-based Chemotherepeutics: A frontier in drug discovery and development. Studies Nat. Burchenal, J. Antileukemic effects of pseudoisocytidine, a new synthetic pyrimidine C-Nucleoside. Cancer Res. Schaeffer, H.

    Combinatorial Chemistry Part B

    Nature , , , Cai, D. Synthesis of C-Nucleoside analogues: 2-[2- Hydroxymethyl -1,3-dioxolanyl]1, 3-thiazolecarboxamide and 2-[2- Mercaptometh- yl -1, 3-dioxolanyl] 1, 3-thiazolecarboxamide. Tripathi, R. Solid phase combinatorial synthesis of carbohydrate-containing ureas with four point diversity. Trends Carbohydr. Tewari, N. Synlett , , 11 , Schmidt, R. Anomeric-oxygen activation for glycoside synthesis: The trichloroacetimidate method.

    Zhu, X. New principles for glycoside-bond formation. Ito, Y. Solid phase oligosaccharide synthesis and related technologies. Manabe, S. Novel nitro wang type linker for polymer support oligosaccharide synthesis; Polymer supported acceptor. Synlett , , 9 , Ghosh, S. Factors influencing ring closure through olefin metathesis-A perspective.

    Grubbs, R. Recent advances in olefin metathesis and its application in organic synthesis. Piscopio, A. Perdih, A. The application of freidinger lactams and their analogs in the design of conformationally constrained peptidomimetics. Solid phase heterocyclic synthesis via ring closing metathesis: traceless linking and cyclative cleavage through a carbon-carbon double bond. Maarseveen, J. Brown, R. Solid phase synthesis of cyclic sulfonamides employing a ring-closing metathesis-cleavage strategy. Shorter, E. Sternbach, L. The benzodiazepine story.

    DeWitt, S. USA , , 90 , Kremen, F. Mayer, J. Solid phase synthesis of 1,4-Benzodiazepine-2,5-diones. Diastereoselective solid phase synthesis of novel hydantoin and isoxazoline-containing heterocycles. Velter, I.

    Carbohydrate based molecular scaffolding. Duffy, R. Rolapitant SCH : A potent, selective and orally active neurokinin NK1 receptor antagonist with centrally-mediated antiemetic effects in ferrets. Lewis, J. Amino acid-derived heterocycles as combinatorial library targets: Bicyclic aminal lactones. Li, Y.

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    High throughput synthesis of 2,3,6-trisubstituted-5,6-dihydroimidazo[2,1-b] thiazole derivatives. Grover, R. Base catalyzed intramolecular transamidation of2-aminoquinazoline derivatives on solid phase. Tetrahedron , , 61 , Kesarwani, A. Solid phase synthesis of imidazoquinazolinone derivatives withthree-point diversity.

    Traceless Solid phase synthesis of bicyclic dihydropyrimidones using multidirectional cyclization cleavage. Myers, A. A solid-supported, enantioselective synthesis suitable for the rapid preparation of large numbers of diverse structural analogues of - -saframycin. Rapamycin AY, , a new antifungal antibiotic. Taxonomy of the producing streptomycete and isolation of the active principle.