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Christopher D Vanderwal

Showing results (41-50 of 92) with videos related to

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The Journal of Organic Chemistry|April 14, 2017
General Approaches to Structurally Diverse IsocyanoditerpenesMary Elisabeth Daub, Philipp C Roosen, Christopher D Vanderwal
Angewandte Chemie (International Ed. in English)|June 20, 2012
A synthesis of echinopine BTheo D Michels, Matthew S Dowling, Christopher D Vanderwal
Journal of Natural Products|February 27, 2008
Interaction of a cyclostreptin analogue with the microtubule taxoid site: the covalent reaction rapidly follows bindingRuoli Bai, Christopher D Vanderwal, J Fernando Díaz, et al.
The Journal of Organic Chemistry|December 16, 2011
Syntheses of strychnine, norfluorocurarine, dehydrodesacetylretuline, and valparicine enabled by intramolecular cycloadditions of Zincke aldehydesDavid B C Martin, Lucas Q Nguyen, Christopher D Vanderwal
Journal of the American Chemical Society|May 2, 2003
An enantioselective synthesis of FR182877 provides a chemical rationalization of its structure and affords multigram quantities of its direct precursorChristopher D Vanderwal, David A Vosburg, Sven Weiler, et al.
Organic Letters|December 1, 2021
Stereocontrolled Synthesis and Structural Revision of Plebeianiol ALucas K Johnson, Scott W Niman, Darius Vrubliauskas, et al.
Journal of the American Chemical Society|March 28, 2015
Synthesis and potent antimalarial activity of kalihinol BMary Elisabeth Daub, Jacques Prudhomme, Karine Le Roch, et al.
Organic Letters|May 4, 2023
Synthesis of a Complex Brasilicardin Analogue Utilizing a Cobalt-Catalyzed MHAT-Induced Radical Bicyclization ReactionScott W Niman, Roberta Buono, David A Fruman, et al.
Organic Letters|June 10, 2010
Concise formal synthesis of porothramycins A and B via Zincke pyridinium ring-opening/ring-closing cascadeTheo D Michels, Matthew J Kier, Aaron M Kearney, et al.
Journal of the American Chemical Society|October 12, 2013
Computation and experiment reveal that the ring-rearrangement metathesis of Himbert cycloadducts can be subject to kinetic or thermodynamic controlJonathan K Lam, Hung V Pham, K N Houk, et al.
Pageof 10

Showing results (41-50 of 92) with videos related to

Sort By:
Pageof 10
The Journal of Organic Chemistry|April 14, 2017
General Approaches to Structurally Diverse IsocyanoditerpenesMary Elisabeth Daub, Philipp C Roosen, Christopher D Vanderwal
Angewandte Chemie (International Ed. in English)|June 20, 2012
A synthesis of echinopine BTheo D Michels, Matthew S Dowling, Christopher D Vanderwal
Journal of Natural Products|February 27, 2008
Interaction of a cyclostreptin analogue with the microtubule taxoid site: the covalent reaction rapidly follows bindingRuoli Bai, Christopher D Vanderwal, J Fernando Díaz, et al.
The Journal of Organic Chemistry|December 16, 2011
Syntheses of strychnine, norfluorocurarine, dehydrodesacetylretuline, and valparicine enabled by intramolecular cycloadditions of Zincke aldehydesDavid B C Martin, Lucas Q Nguyen, Christopher D Vanderwal
Journal of the American Chemical Society|May 2, 2003
An enantioselective synthesis of FR182877 provides a chemical rationalization of its structure and affords multigram quantities of its direct precursorChristopher D Vanderwal, David A Vosburg, Sven Weiler, et al.
Organic Letters|December 1, 2021
Stereocontrolled Synthesis and Structural Revision of Plebeianiol ALucas K Johnson, Scott W Niman, Darius Vrubliauskas, et al.
Journal of the American Chemical Society|March 28, 2015
Synthesis and potent antimalarial activity of kalihinol BMary Elisabeth Daub, Jacques Prudhomme, Karine Le Roch, et al.
Organic Letters|May 4, 2023
Synthesis of a Complex Brasilicardin Analogue Utilizing a Cobalt-Catalyzed MHAT-Induced Radical Bicyclization ReactionScott W Niman, Roberta Buono, David A Fruman, et al.
Organic Letters|June 10, 2010
Concise formal synthesis of porothramycins A and B via Zincke pyridinium ring-opening/ring-closing cascadeTheo D Michels, Matthew J Kier, Aaron M Kearney, et al.
Journal of the American Chemical Society|October 12, 2013
Computation and experiment reveal that the ring-rearrangement metathesis of Himbert cycloadducts can be subject to kinetic or thermodynamic controlJonathan K Lam, Hung V Pham, K N Houk, et al.
Pageof 10