Search Results - Pojarliev, Peter

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  1. 1
    Efficient Proline-Catalyzed Michael Additions of Unmodified Ketones to Nitro Olefins

    Efficient Proline-Catalyzed Michael Additions of Unmodified Ketones to Nitro Olefins by List, Benjamin, Pojarliev, Peter, Martin, Harry J

    Published in Organic letters
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  2. 2
    The Proline-Catalyzed Direct Asymmetric Three-Component Mannich Reaction:  Scope, Optimization, and Application to the Highly Enantioselective Synthesis of 1,2-Amino Alcohols

    The Proline-Catalyzed Direct Asymmetric Three-Component Mannich Reaction:  Scope, Optimization, and Application to the Highly Enantioselective Synthesis of 1,2-Amino Alcohols by List, Benjamin, Pojarliev, Peter, Biller, William T, Martin, Harry J

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  3. 3
    Proline-Catalyzed Asymmetric Aldol Reactions between Ketones and α-Unsubstituted Aldehydes

    Proline-Catalyzed Asymmetric Aldol Reactions between Ketones and α-Unsubstituted Aldehydes by List, Benjamin, Pojarliev, Peter, Castello, Chris

    Published in Organic letters
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  4. 4
    Highly Enantioselective Synthesis of 1,2-Amino Alcohol Derivatives via Proline-Catalyzed Mannich Reaction

    Highly Enantioselective Synthesis of 1,2-Amino Alcohol Derivatives via Proline-Catalyzed Mannich Reaction by Pojarliev, Peter, Biller, William T., Martin, Harry J., List, Benjamin

    Published in Synlett
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  5. 5
    A novel highly stereoselective total synthesis of epothilone B and of its (12 R,13 R) acetonide

    A novel highly stereoselective total synthesis of epothilone B and of its (12 R,13 R) acetonide by Mulzer, Johann, Karig, Gunter, Pojarliev, Peter

    Published in Tetrahedron letters
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  6. 6
    The 12,13-Diol Cyclization Approach for a Truly Stereocontrolled Total Synthesis of Epothilone B and the Synthesis of a Conformationally Restrained Analogue

    The 12,13-Diol Cyclization Approach for a Truly Stereocontrolled Total Synthesis of Epothilone B and the Synthesis of a Conformationally Restrained Analogue by Martin, Harry J., Pojarliev, Peter, Kählig, Hanspeter, Mulzer, Johann

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  7. 7
    Aminoalcohols V [1]: A Methodfor the Synthesis of EnantiomericallyPure Ring-Chlorinated Epinephrinesand Norepinephrines

    Aminoalcohols V [1]: A Methodfor the Synthesis of EnantiomericallyPure Ring-Chlorinated Epinephrinesand Norepinephrines by Knollmüller, Max, Gärtner, Peter, Pernerstorfer, Josef, Pojarliev, Peter, Stegmann, Hartmut B.

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  8. 8
    Aminoalkohole, 5. Mitt. [1]: Ein Verfahren zur Synthese von enantiomerenreinenkernchlorierten Epinephrinen und Norepinephrinen

    Aminoalkohole, 5. Mitt. [1]: Ein Verfahren zur Synthese von enantiomerenreinenkernchlorierten Epinephrinen und Norepinephrinen by Knollmüller, Max, Gärtner, Peter, Pernerstorfer, Josef, Pojarliev, Peter, Stegmann, Hartmut B.

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