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Peptidomimetics and Mimicry of -Strand / Sheets and -Sheet Sandwiches Jian Liu Merck & Co., Inc. Rahway, NJ 07065
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Research Summary Pyrrolinone -Strand Peptidomimetic HIV-1 Protease Inhibitor 1999-present UPenn -Sheet Sandwich 1998-1999 UC Irvine Cycloaddition of Enol Ethers 1994-1998 UCLA Enantioselective Epoxidation
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Part I a.Computational Study on Epoxidation Reactions b. Conformational Switch for Enol Ethers in Cycloaddition Reactions
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Reaction Path Investigation by Computational Methods
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Epoxidations of Unfunctionalized Olefins Liu, J., Houk, K. N. et. al. J. Am. Chem. Soc. 1997, 119, 3385-3386; J. Am. Chem. Soc. 1997, 119, 10147-10152; J. Am. Chem. Soc. 1997, 119, 12982-12983; J. Org. Chem. 1998, 63, 8565-8569
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Part I a.Computational Study on Epoxidation Reactions b. Conformational Switch for Enol Ethers in Cycloaddition Reactions
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Conformational Switch in Cycloaddition of Enol Ethers s-cis in ground states-trans in transition state Liu, J.; Niwayama, S.; You, Y.; Houk, K. N. J. Org. Chem. 1998, 63, 1064.
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Stereoselective Cycloaddition Reactions of Chiral Enol Ether Denmark, S. E. et. al. J. Org. Chem. 1994, 59, 5672; 1995, 60, 3205; 1995, 60, 3574. Reissig, H. U. et. al. SYNLETT 1990, 514; Angew. Chem. Int. Ed. Engl. 1992, 31, 1033.
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Ground State Conformations of Chiral Enol Ethers
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Conformations of Vinyl Methyl Ether in Ground and Transition States
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Design of Conformation Fixed Enol Ethers trans cis
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Designed Diels-Alder Reactions with the Conformation Fixed Enol Ethers
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Designed 1,3-dipolar Cycloaddition With the Conformation Fixed Enol Ethers
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Comparison of the Calculated and Experimental Results
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Rationalization of Conformation Switch
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Summary for Ph.D Research at UCLA a. Computation study on epoxidation reaction: b. Conformation switch of enol ether in cycloaddition reaction:
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Part II Design, Synthesis and Structure Study of Artificial -Sheet Sandwiches
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Previous Study on Artificial -Sheet Structures Nowick, J. S. et al J. Org. Chem. 1997, 62, 7906-7907. Nowick, J. S. et al Chem. Soc. Rev. 1996, 25, 401-415. Nowick, J. S. Acc. Chem. Res. 1999, 32, 287-296.
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The Importance of the -Sheet Sandwich in Nature Definition: The -Sheet sandwich is a structure motif in proteins in which two -sheets face each other to form a sandwich. The -sheet sandwich can act as a binding pocket. Goal of building the artificial -sheet sandwich: To build a chemical model to mimic the three dimensional structures of globular proteins. Lipid binding protein: 1lif
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Design of an Artificial -Sheet Sandwich Hydrophilic Back Hydrophobic Face
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Synthesis of a Model with one Template Holding two -Turn Scaffold Structures
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Synthesis of a Model with One Template Holding Two -Turn Scaffold Structures (Cont.)
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Crystal Structure of the Model with a Template Holding Two -Turn Scaffolds
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Synthesis of the Designed -Sheet Sandwich
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Synthesis of the Designed -Sheet Sandwich (Cont.)
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Two Dimensional TLC Test on the Interconvergence of Different Conformations for -Sheet Sandwich 11
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Possible Conformations for -Sheet Sandwich Back - FaceFace - Face Back - BackFace - Back
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New Design for -Sheet Sandwich with an Additional Linkage between -Sheets
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Synthesis of -Sheet Sandwich with S-S Linkage
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Synthesis of -Sheet Sandwich with S-S Linkage (Cont.)
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Synthesis of -Sheet Sandwich with C-C Linkage Metathesis Product: ( 3 : 1, trans to cis )
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NMR Study of the -Sheet Sandwiches with C=C Linkage No Inter Sheet NOEs Observed Inter Sheet NOEs: H 15 - H 18 ; H 15 - H 20 ; H 18 - H 19 ; H 23 - H 27 ; H 26 - H 21 ; H 27 - H 21.
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Summary of Postdoc Research at UC Irvine a. Designed and synthesized the artificial -sheet sandwich: b. Designed and synthesized the -sheet sandwich with homogenous conformation:
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Part III Design, Synthesis and Structure Study of -Strand Peptidomimetic Based on Pyrrolinone Backbone
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Concept for the Design of -Strand Peptidomimetic Based on Pyrrolinone Backbone
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Precigoux, G et. al. J. Am. Chem. Soc. 1987, 109, 7463. Smith, A. B. III; Hirschmann, R. et. al. J. Am. Chem. Soc. 1994, 116, 9947. Peptides and Peptidomimetics Which Forms -Strand/Sheets
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Retrosynthesis of Tris Carbonyl Displaced Pyrrolinone
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Synthesis of Fragment A and B
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Synthesis of Fragment D S. Knight
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Synthesis of Fragment C S. Knight
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Synthesis of Mono Pyrrolinone S. Knight
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Synthesis of Bis Pyrrolinone
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Synthesis of Tris Pyrrolinone
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Synthesis of Tris Pyrrolinone (Cont.)
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Part IV Design and Synthesis of Pyrrolinone Based HIV-1 Protease Inhibitor
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Previous Peptidomimetic HIV-1 Protease Inhibitors Smith, A. B., III, Pasternak, A., Hirschmann, R. et. al. J. Med. Chem. 1997, 40, 2440-2444
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Retrosynthesis of Second Generation Carbonyl Displaced Pyrrolinone HIV-1 Protease Inhibitor
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Synthesis of Carbonyl Displaced Pyrrolinone HIV-1 Protease Inhibitor
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X-Ray Crystal Structure of HIV-1 Protease Complexed with Inhibitor A. Pasternak
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X-Ray Crystal Structure of HIV-1 Protease Complexed with Inhibitor L. Zawaki
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Design of New Carbonyl Displaced Pyrrolinone HIV-1 Protease Inhibitor
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Summary of Postdoc Research at UPenn a. The tris carbonyl-displaced pyrrolinone was synthesized and the structure is being studied: b. A carbonyl-displaced pyrrolinone HIV-1 protease inhibitor was designed and synthesized. A new design was made based on modeling:
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Acknowledgements Professor Ken N. Houk (UCLA) Professor James S. Nowick (UC Irvine) Professor Amos B. Smith, III (UPenn) Professor Ralph Hirschmann (UPenn)
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Thank You
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