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Uli Kazmaier

Showing results (1-10 of 133) with videos related to

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The Journal of Organic Chemistry|May 31, 1996
Application of the Ester Enolate Claisen Rearrangement in the Synthesis of Amino Acids Containing Quaternary Carbon CentersUli Kazmaier
Marine Drugs|January 24, 2025
Syntheses of Marine Natural Products via Matteson Homologations and Related ProcessesUli Kazmaier
Organic Letters|March 28, 2022
Stereoselective Synthesis of a Protected Side Chain of Meliponamycin AOliver Andler, Uli Kazmaier
The Journal of Organic Chemistry|October 6, 2012
Synthesis of tubuphenylalanines via Ireland-Claisen rearrangementDominic Becker, Uli Kazmaier
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 12, 2025
Stereoselective Syntheses of Highly Substituted Tetrahydrofurans based on Matteson HomologationsMarkus Tost, Uli Kazmaier
Organic & Biomolecular Chemistry|October 15, 2024
Syntheses of bottromycin derivatives <i>via</i> Ugi-reactions and Matteson homologationsEtienne Bickel, Uli Kazmaier
The Journal of Organic Chemistry|March 5, 2013
Isolation of an σ-alkyl iridium hydride complex, formed in the (semi)hydrogenation of an β-enamido ketoneFrauke Maurer, Uli Kazmaier
Organic & Biomolecular Chemistry|January 13, 2010
Diastereotopos-differentiating allylic alkylation as a key step in the synthesis of gamma-glutamyl boletineDnyaneshwar Gawas, Uli Kazmaier
The Journal of Organic Chemistry|January 8, 2009
Highly diastereoselective anti-aldol reactions of glycolate titanium enolatesDnyaneshwar Gawas, Uli Kazmaier
Organic Letters|December 26, 2023
Matteson Homologation-Based Total Synthesis of Meliponamycin AOliver Andler, Uli Kazmaier
Pageof 14

Showing results (1-10 of 133) with videos related to

Sort By:
Pageof 14
The Journal of Organic Chemistry|May 31, 1996
Application of the Ester Enolate Claisen Rearrangement in the Synthesis of Amino Acids Containing Quaternary Carbon CentersUli Kazmaier
Marine Drugs|January 24, 2025
Syntheses of Marine Natural Products via Matteson Homologations and Related ProcessesUli Kazmaier
Organic Letters|March 28, 2022
Stereoselective Synthesis of a Protected Side Chain of Meliponamycin AOliver Andler, Uli Kazmaier
The Journal of Organic Chemistry|October 6, 2012
Synthesis of tubuphenylalanines via Ireland-Claisen rearrangementDominic Becker, Uli Kazmaier
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 12, 2025
Stereoselective Syntheses of Highly Substituted Tetrahydrofurans based on Matteson HomologationsMarkus Tost, Uli Kazmaier
Organic & Biomolecular Chemistry|October 15, 2024
Syntheses of bottromycin derivatives <i>via</i> Ugi-reactions and Matteson homologationsEtienne Bickel, Uli Kazmaier
The Journal of Organic Chemistry|March 5, 2013
Isolation of an σ-alkyl iridium hydride complex, formed in the (semi)hydrogenation of an β-enamido ketoneFrauke Maurer, Uli Kazmaier
Organic & Biomolecular Chemistry|January 13, 2010
Diastereotopos-differentiating allylic alkylation as a key step in the synthesis of gamma-glutamyl boletineDnyaneshwar Gawas, Uli Kazmaier
The Journal of Organic Chemistry|January 8, 2009
Highly diastereoselective anti-aldol reactions of glycolate titanium enolatesDnyaneshwar Gawas, Uli Kazmaier
Organic Letters|December 26, 2023
Matteson Homologation-Based Total Synthesis of Meliponamycin AOliver Andler, Uli Kazmaier
Pageof 14