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Alberto Marco

Showing results (1-10 of 89) with videos related to

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Natural Product Communications|May 13, 2011
Stereoselective synthesis of five biologically active, naturally occurring medium and large ring lactonesJ Alberto Marco, Miguel Carda
The Journal of Organic Chemistry|September 4, 2008
Short, stereoselective synthesis of the naturally occurring pyrrolidine radicamine B and a formal synthesis of nectrisineCelia Ribes, Eva Falomir, Miguel Carda, et al.
The Journal of Organic Chemistry|January 18, 2005
Stereoselective synthesis of the naturally occurring styryllactones (+)-goniofufurone and (+)-cardiobutanolidePurificación Ruiz, Juan Murga, Miguel Carda, et al.
Organic Letters|December 29, 2006
Stereoselective synthesis of the glycosidase inhibitor australine through a one-pot, double-cyclization strategyCelia Ribes, Eva Falomir, Miguel Carda, et al.
The Journal of Organic Chemistry|August 31, 2002
Stereoselective synthesis of (+)-boronolideMiguel Carda, Santiago Rodríguez, Beatriz Segovia, et al.
Planta Medica|March 8, 2003
Jatrophane diterpenes from the latex of Euphorbia obtusifolia with inhibitory activity on the mammalian mitochondrial respiratory chainLiliana Betancur-Galvis, Javier Checa, J Alberto Marco, et al.
The Journal of Organic Chemistry|October 9, 2004
Stereoselective synthesis of the antiprotozoal lactone passifloricin A and seven isomers thereofJuan Murga, Jorge García-Fortanet, Miguel Carda, et al.
The Journal of Organic Chemistry|July 15, 2006
Stereoselective synthesis of the published structure of feigrisolide A. Structural revision of feigrisolides A and BPaula Alvarez-Bercedo, Juan Murga, Miguel Carda, et al.
Organic Letters|June 16, 2006
Stereoselective synthesis of the cytotoxic macrolide FD-891Jorge García-Fortanet, Juan Murga, Miguel Carda, et al.
Journal of Ethnopharmacology|March 18, 2003
Tigliane diterpenes from the latex of Euphorbia obtusifolia with inhibitory activity on the mammalian mitochondrial respiratory chainLiliana Betancur-Galvis, Emilio Palomares, J Alberto Marco, et al.
Pageof 9

Showing results (1-10 of 89) with videos related to

Sort By:
Pageof 9
Natural Product Communications|May 13, 2011
Stereoselective synthesis of five biologically active, naturally occurring medium and large ring lactonesJ Alberto Marco, Miguel Carda
The Journal of Organic Chemistry|September 4, 2008
Short, stereoselective synthesis of the naturally occurring pyrrolidine radicamine B and a formal synthesis of nectrisineCelia Ribes, Eva Falomir, Miguel Carda, et al.
The Journal of Organic Chemistry|January 18, 2005
Stereoselective synthesis of the naturally occurring styryllactones (+)-goniofufurone and (+)-cardiobutanolidePurificación Ruiz, Juan Murga, Miguel Carda, et al.
Organic Letters|December 29, 2006
Stereoselective synthesis of the glycosidase inhibitor australine through a one-pot, double-cyclization strategyCelia Ribes, Eva Falomir, Miguel Carda, et al.
The Journal of Organic Chemistry|August 31, 2002
Stereoselective synthesis of (+)-boronolideMiguel Carda, Santiago Rodríguez, Beatriz Segovia, et al.
Planta Medica|March 8, 2003
Jatrophane diterpenes from the latex of Euphorbia obtusifolia with inhibitory activity on the mammalian mitochondrial respiratory chainLiliana Betancur-Galvis, Javier Checa, J Alberto Marco, et al.
The Journal of Organic Chemistry|October 9, 2004
Stereoselective synthesis of the antiprotozoal lactone passifloricin A and seven isomers thereofJuan Murga, Jorge García-Fortanet, Miguel Carda, et al.
The Journal of Organic Chemistry|July 15, 2006
Stereoselective synthesis of the published structure of feigrisolide A. Structural revision of feigrisolides A and BPaula Alvarez-Bercedo, Juan Murga, Miguel Carda, et al.
Organic Letters|June 16, 2006
Stereoselective synthesis of the cytotoxic macrolide FD-891Jorge García-Fortanet, Juan Murga, Miguel Carda, et al.
Journal of Ethnopharmacology|March 18, 2003
Tigliane diterpenes from the latex of Euphorbia obtusifolia with inhibitory activity on the mammalian mitochondrial respiratory chainLiliana Betancur-Galvis, Emilio Palomares, J Alberto Marco, et al.
Pageof 9