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Juan F Sanz-Cervera

Showing results (1-10 of 30) with videos related to

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Journal of the American Chemical Society|March 14, 2002
Asymmetric total synthesis of (-)-VM55599: establishment of the absolute stereochemistry and biogenetic implicationsJuan F Sanz-Cervera, Robert M Williams
Angewandte Chemie (International Ed. in English)|May 2, 2018
Reverse versus Normal Prenyl Transferases in Paraherquamide Biosynthesis Exhibit Distinct Facial SelectivitiesEmily M Stocking, Juan F Sanz-Cervera, Robert M Williams
Angewandte Chemie (International Ed. in English)|April 13, 2001
Studies on the Biosynthesis of Paraherquamide: Synthesis and Incorporation of a Hexacyclic Indole Derivative as an Advanced Metabolite This work was supported by the National Institutes of Health (Grant no. CA70375 to R.M.W.). We wish to acknowledge the American Chemical Society Division of Organic Chemistry Fellowship (sponsored by SmithKline Beecham) and the Pharmacia-Upjohn Company for financial support (to E.M.S.). Mass spectra were obtained on instruments supported by the National Institutes of Health Shared Instrumentation Grant (No. GM49631). We also wish to thank Professor Dean Crick of the Department of Microbiology at Colorado State University for helpful discussions. J.F.S.-C. thanks the DGICYT of Spain for a research grant (project no. PB98-1438)Emily M. Stocking, Juan F. Sanz-Cervera, Robert M. Williams
Chemical Communications (Cambridge, England)|May 13, 2003
An efficient synthesis of new fluorinated uracil derivativesSantos Fustero, Esther Salavert, Juan F Sanz-Cervera, et al.
The Journal of Organic Chemistry|July 11, 2009
Fluorous TBAF: a convenient and selective reagent for fluoride-mediated deprotectionsSantos Fustero, Amador García Sancho, José Luis Aceña, et al.
The Journal of Organic Chemistry|March 8, 1996
Terracinolides A and B, Two Bishomoditerpene Lactones with a Novel Carbon Framework from Euphorbia terracinaJ. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste, et al.
Organic Letters|January 24, 2008
An efficient entry to optically active anti- and syn-beta-amino-alpha-trifluoromethyl alcoholsSantos Fustero, Laia Albert, José Luis Aceña, et al.
Phytochemistry|July 19, 2005
Sesquiterpenes from Centaurea asperaJ Alberto Marco, Juan F Sanz-Cervera, Alberto Yuste, et al.
Journal of the American Chemical Society|December 3, 2003
Studies on the biosynthesis of asperparaline A: origin of the spirosuccinimde ring systemChandele R Gray, Juan F Sanz-Cervera, Louis A Silks, et al.
Organic Letters|April 23, 2004
A versatile synthesis of fluorinated uracils in solution and on solid-phaseSantos Fustero, Julio Piera, Juan F Sanz-Cervera, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Journal of the American Chemical Society|March 14, 2002
Asymmetric total synthesis of (-)-VM55599: establishment of the absolute stereochemistry and biogenetic implicationsJuan F Sanz-Cervera, Robert M Williams
Angewandte Chemie (International Ed. in English)|May 2, 2018
Reverse versus Normal Prenyl Transferases in Paraherquamide Biosynthesis Exhibit Distinct Facial SelectivitiesEmily M Stocking, Juan F Sanz-Cervera, Robert M Williams
Angewandte Chemie (International Ed. in English)|April 13, 2001
Studies on the Biosynthesis of Paraherquamide: Synthesis and Incorporation of a Hexacyclic Indole Derivative as an Advanced Metabolite This work was supported by the National Institutes of Health (Grant no. CA70375 to R.M.W.). We wish to acknowledge the American Chemical Society Division of Organic Chemistry Fellowship (sponsored by SmithKline Beecham) and the Pharmacia-Upjohn Company for financial support (to E.M.S.). Mass spectra were obtained on instruments supported by the National Institutes of Health Shared Instrumentation Grant (No. GM49631). We also wish to thank Professor Dean Crick of the Department of Microbiology at Colorado State University for helpful discussions. J.F.S.-C. thanks the DGICYT of Spain for a research grant (project no. PB98-1438)Emily M. Stocking, Juan F. Sanz-Cervera, Robert M. Williams
Chemical Communications (Cambridge, England)|May 13, 2003
An efficient synthesis of new fluorinated uracil derivativesSantos Fustero, Esther Salavert, Juan F Sanz-Cervera, et al.
The Journal of Organic Chemistry|July 11, 2009
Fluorous TBAF: a convenient and selective reagent for fluoride-mediated deprotectionsSantos Fustero, Amador García Sancho, José Luis Aceña, et al.
The Journal of Organic Chemistry|March 8, 1996
Terracinolides A and B, Two Bishomoditerpene Lactones with a Novel Carbon Framework from Euphorbia terracinaJ. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste, et al.
Organic Letters|January 24, 2008
An efficient entry to optically active anti- and syn-beta-amino-alpha-trifluoromethyl alcoholsSantos Fustero, Laia Albert, José Luis Aceña, et al.
Phytochemistry|July 19, 2005
Sesquiterpenes from Centaurea asperaJ Alberto Marco, Juan F Sanz-Cervera, Alberto Yuste, et al.
Journal of the American Chemical Society|December 3, 2003
Studies on the biosynthesis of asperparaline A: origin of the spirosuccinimde ring systemChandele R Gray, Juan F Sanz-Cervera, Louis A Silks, et al.
Organic Letters|April 23, 2004
A versatile synthesis of fluorinated uracils in solution and on solid-phaseSantos Fustero, Julio Piera, Juan F Sanz-Cervera, et al.
Pageof 3