J. Marco

发表

2.14 Selected Diastereoselective Reactions: Enolate Alkylation

M. Carda, E. Falomir, J. Marco, 2012 .

Double diastereoselection in anti aldol reactions mediated by dicyclohexylchloroborane between an L-erythrulose derivative and chiral aldehydes.

M. Carda, E. Falomir, J. Marco, 2012, Organic & biomolecular chemistry.

Aldol reactions between L-erythrulose derivatives and chiral alpha-amino and alpha-fluoro aldehydes: competition between Felkin-Anh and Cornforth transition states.

M. Carda, E. Falomir, J. Marco, 2008, Chemistry.

Synthesis and biological properties of the cytotoxic 14-membered macrolides aspergillide A and B.

M. Carda, E. Falomir, J. Marco, 2011, Chemistry.

Stereoselective syntheses of naturally occurring 5,6-dihydropyran-2-ones

M. Carda, E. Falomir, J. Marco, 2007 .

The total synthesis and biological properties of the cytotoxic macrolide FD-891 and its non-natural (Z)-C12 isomer.

I. Barasoain, J. Díaz, J. F. Díaz, 2007, Chemistry.

Stereoselective synthesis of the C14–C26 fragment of the cytotoxic macrolide FD-891

M. Carda, J. Marco, J. Murga, 2004 .

Sesquiterpene lactones from iranian Artemisia species

F. Sancenón, A. Rustaiyan, J. Marco, 1993 .

Synthesis and evaluation of biphenyl derivatives as potential downregulators of VEGF protein secretion and telomerase-related gene expressions.

M. Carda, E. Falomir, J. Marco, 2016, Bioorganic & medicinal chemistry.

Two isorhamnetin triglycosides from Anthyllis sericea

V. Wray, D. Strack, J. Marco, 1989 .

Flavonoid glycosides from Anthyllis sericea

J. Marco, J. Adell, O. Barberá, 1988 .

Interactions of long-chain homologues of colchicine with tubulin.

G. Breuzard, P. Barbier, Diane Allegro, 2017, European journal of medicinal chemistry.

Synthesis and biological evaluation of truncated α-tubulin-binding pironetin analogues lacking alkyl pendants in the side chain or the dihydropyrone ring.

M. Redondo-Horcajo, I. Barasoain, M. Carda, 2013, Organic & biomolecular chemistry.

Synthesis and Biological Evaluation of α‐Tubulin‐Binding Pironetin Analogues with Enhanced Lipophilicity

I. Barasoain, M. Carda, E. Falomir, 2013 .

Synthesis and biological evaluation as microtubule-active agents of several tetrahydrofuran and spiroacetal derivatives.

M. Redondo-Horcajo, I. Barasoain, M. Carda, 2013, Current medicinal chemistry.

Design and synthesis of pironetin analogues with simplified structure and study of their interactions with microtubules.

I. Barasoain, J. Díaz, M. Carda, 2011, European journal of medicinal chemistry.

syn-1,6:8,13-diimino[14]annulene

E. Vogel, J. Marco, R. Aydin, 1983 .

Recent Advances in the Field of Naturally Occurring 5,6‐Dihydropyran‐2‐ones

M. Carda, J. Marco, 2013 .

Diterpenes from Euphorbia paralias

W. Berendsohn, J. Marco, J. Jakupovic, 1998 .

Jatrophane derivatives and a rearranged jatrophane from Euphorbia terracina

J. Marco, J. Jakupovic, J. F. Sanz-Cervera, 1998 .

Comparative Analysis of the Vascular Actions of Diterpenes Isolated from Euphorbia canariensis

E. Alborch, J. Marco, J. M. Centeno, 1998, The Journal of pharmacy and pharmacology.

Terracinolides A and B, Two Bishomoditerpene Lactones with a Novel Carbon Framework from Euphorbia terracina.

J. Lex, J. Marco, J. Jakupovic, 1996, The Journal of organic chemistry.

Influence of structural factors and enzyme type on the reactivity and enantioselectivity of the enzymatic esterification of bicyclic meso dialcohols

G. Asensio, J. Marco, C. Andreu, 1992 .

Synthesis and biological evaluation of cyclic derivatives of combretastatin A-4 containing group 14 elements.

M. Carda, E. Falomir, S. Royo, 2018, Organic & biomolecular chemistry.

The Mechanism of the Interactions of Pironetin Analog/Combretastatin A‐4 Hybrids with Tubulin

M. Redondo-Horcajo, I. Barasoain, J. Díaz, 2015, Archiv der Pharmazie.

Silphinene Sesquiterpenes as Model Insect Antifeedants

A. González-Coloma, J. Hoffmann, J. Marco, 2004, Journal of Chemical Ecology.

Stereoselective synthesis of (-)-malyngolide, (+)-malyngolide and (+)-tanikolide using ring-closing metathesis

M. Carda, J. Marco, S. Díaz-Oltra, 2003 .

Erythrulose derivatives as functionalized chiral d3 and d4 synthons

M. Carda, E. Falomir, J. Marco, 2002 .

Stereoselective synthesis of (−)-cytoxazone

M. Carda, J. Marco, F. González, 2002 .

Synthesis of (±)-(E)-2,6-dimethyl-6-hydroxyocta-2,7-dienoic acid and the corresponding amide (“acacialactam”)

M. Carda, J. Marco, J. Murga, 1994 .

Arylpyridines, arylpyrimidines and related compounds as potential modulator agents of the VEGF, hTERT and c-Myc oncogenes.

M. Carda, E. Falomir, J. Marco, 2019, Bioorganic & medicinal chemistry.

Analysis of Rabbit Vascular Responses to DBI, an Ingol Derivative Isolated from Euphorbia canariensis

E. Alborch, J. Marco, J. M. Centeno, 1997, The Journal of pharmacy and pharmacology.

Synthesis and Biological Evaluation of Imines Structurally Related to Resveratrol as Dual Inhibitors of VEGF Protein Secretion and hTERT Gene Expression1

M. Carda, R. Martí-Centelles, E. Falomir, 2017, Natural product communications.

Diterpenes from Euphorbia segetalis

W. Berendsohn, J. Marco, J. Jakupovic, 1998 .

Diastereoselective additions of organolithium and organomagnesium reagents to the CN bond of a chiral, cyclic nitrone derived from erythrulose

J. Lex, M. Carda, E. Falomir, 1998 .

Diastereoselective additions of organolithium reagents to the CN bond of protected erythrulose oxime ethers. Synthesis of enantiopure α,α-disubstituted α-aminiacids

M. Carda, E. Falomir, J. Marco, 1997 .

Carbon-13 NMR spectroscopy of sesquiterpenes. 3. Synthesis and carbon-13 NMR spectral data of 4.alpha.,5.alpha.- and 4.beta.,5.beta.-epoxyeudesmanolides. Configuration and .gamma. effect of the oxirane ring

M. Carda, J. Marco, J. F. Sanz, 1992 .

Xanthanolides from Xanthium: absolute configuration of xanthanol, isoxanthanol and their C-4 epimers

M. Carda, J. Marco, Julia Corral, 1993 .

Design, synthesis and antimalarial evaluation of novel thiazole derivatives.

M. Carda, Benigno Crespo, María L León, 2016, Bioorganic & medicinal chemistry letters.

Influence of the protecting groups on the syn/anti stereoselectivity of boron aldol additions with erythrulose derivatives. A theoretical and experimental study

M. Carda, E. Falomir, Juan Murga, 2002 .

Boron aldol additions with erythrulose derivatives: dependence of stereoselectivity on the type of protecting group

M. Carda, E. Falomir, J. Marco, 1999 .

Erythrulose as a multifunctional chiron: Highly stereoselective boron aldol additions

A. Linden, M. Carda, E. Falomir, 1999 .

Diastereoselectivity of the reactions of organolithium reagents with protected erythrulose oximes

M. Carda, E. Falomir, J. Marco, 1998 .

Synthesis of conjugated δ-lactams using ring-closing metathesis

M. Carda, J. Marco, S. Rodríguez, 2002 .

Stereoselective synthesis of (+)-boronolide.

M. Carda, J. Marco, S. Rodríguez, 2002, The Journal of organic chemistry.

Stereoselective indium-mediated allylation of erythrulose derivatives in aqueous media

M. Carda, J. Marco, J. Murga, 1998 .

Stereoselective Synthesis of Five Biologically Active, Naturally Occurring Medium and Large Ring Lactones

M. Carda, J. Marco, 2011 .

Inhibition of VEGF expression in cancer cells and endothelial cell differentiation by synthetic stilbene derivatives.

M. Carda, R. Martí-Centelles, E. Falomir, 2013, Bioorganic & medicinal chemistry.

Stereoselective synthesis of hyptolide and 6-epi-hyptolide

M. Carda, J. Marco, J. Murga, 2004 .

Asymmetric synthesis of passifloricin A: a correction in structure

M. Carda, J. Marco, J. Murga, 2003 .

On the structure of passifloricin A: asymmetric synthesis of the delta-lactones of (2Z,5S,7R,9S,11S)- and (2Z,5R,7R,9S,11S)tetrahydroxyhexacos-2-enoic acid.

M. Carda, J. Marco, J. Murga, 2003, Organic letters.

Stereoselective synthesis of (+)-hyptolide

M. Carda, J. Marco, J. Murga, 2003 .

Stereoselective synthesis of spicigerolide

M. Carda, E. Falomir, J. Marco, 2003 .

Stereoselective synthesis of the cytotoxic macrolide aspergillide B

M. Carda, M. Kneeteman, J. Marco, 2009 .

Phenolic and acetylenic metabolites from Artemisia assoana

J. Marco, O. Barberá, V. Martinez, 1987 .

Synthesis of conjugated γ- and δ-lactones from aldehydes and ketones via a vinylation(allylation)-ring closing metathesis–oxidation sequence

M. Carda, M. Kneeteman, J. Marco, 2003 .

Stereoselective syntheses of the glycosidase inhibitors hyacinthacine A2, hyacinthacine A3 and 5-epi-hyacinthacine A3

M. Carda, E. Falomir, J. Marco, 2009 .

Stereoselective synthesis of the glycosidase inhibitor australine through a one-pot, double-cyclization strategy.

M. Carda, E. Falomir, J. Marco, 2007, Organic letters.

Stereoselective addition of organometallic reagents to a chiral acyclic nitrone derived from l-erythrulose

M. Carda, E. Falomir, J. Marco, 2005 .

Synthesis of α,α-Disubstituted α-Amino Acid Derivatives in Enantiopure Form via Stereoselective Addition of Grignard Reagents to a Chiral Acyclic Nitrone Derived from l-Erythrulose

M. Carda, E. Falomir, S. Uriel, 2002 .

A stereoselective synthesis of (+)-malyngolide via a ring-closing olefin metathesis

M. Carda, J. Marco, S. Rodríguez, 2000 .

Stereoselective allylations of erythrulose derivatives under anhydrous conditions

M. Carda, J. Marco, F. González, 2001 .

The Stereoselective Synthesis of the Nonnatural Enantiomers of Communiols A-C. A Stereochemical Correction

M. Carda, E. Falomir, J. Marco, 2006 .

Stereoselective synthesis and determination of the cytotoxic properties of spicigerolide and three of its stereoisomers.

M. Carda, E. Falomir, J. Marco, 2003, The Journal of organic chemistry.

Synthesis and biological evaluation of simplified pironetin analogues with modifications in the side chain and the lactone ring.

M. Carda, E. Falomir, J. Marco, 2016, Organic & biomolecular chemistry.

Título artículo / Títol article: Design and Synthesis of Pironetin Analogue/Colchicine Hybrids and Study of Their Cytotoxic Activity and Mechanisms of Interaction with Tubulin

M. Redondo-Horcajo, I. Barasoain, M. Carda, 2014 .

Design and Synthesis of Pironetin Analogue/Combretastatin A‐4 Hybrids and Evaluation of Their Cytotoxic Activity

M. Carda, E. Falomir, S. Torijano-Gutiérrez, 2014 .

Stereoselective Synthesis of the Naturally Occurring Lactones(−)‐Osmundalactone and (−)‐Muricatacine Using Ring‐Closing Metathesis

M. Carda, J. Marco, F. González, 2002 .

Boron Aldol Additions with Erythrulose Derivatives: Dependence of Stereoselectivity on the Type of Protecting Group.

M. Carda, E. Falomir, J. Marco, 1999 .

An ab initio study of the enolboration of 3-pentanone mediated by boron monochlorides L2BCl

M. Carda, E. Falomir, Juan Murga, 2001 .

SYNTHESIS OF (E)-2,6-DIMETHYL-6-HYDROXYOCTA-2,7-DIENOIC ACID AND THE CORRESPONDING AMIDE ( ACACIALACTAM ) IN OPTICALLY ACTIVE FORM

M. Carda, J. Marco, J. Murga, 1995 .

Diastereoselective synthesis of enantiomeric tertiary alcohols via nucleophilic additions to protected D- and L-erythrulose derivatives

M. Carda, J. Marco, F. González, 1992 .

Stereoselective synthesis of pachastrissamine (jaspine B)

M. Carda, E. Falomir, J. Marco, 2006 .

Stereoselective synthesis of microcarpalide.

M. Carda, E. Falomir, J. Marco, 2002, Organic letters.

Stereoselective synthesis of the cytotoxic macrolide FD-891.

M. Carda, J. Marco, J. Murga, 2006, Organic letters.

Tricyclic sesquiterpenes from Artemisia chamaemelifolia

J. Marco, J. Jakupovic, J. F. Sanz-Cervera, 1996 .

Enzyme-mediated enantioselective acylation of secondary amines in organic solvents

G. Asensio, J. Marco, C. Andreu, 1991 .

Diastereoselectivity of the Reactions of Organolithium Reagents with Protected Erythrulose Oximes.

M. Carda, E. Falomir, J. Marco, 1998 .

Synthesis of Conjugated δ‐Lactams Using Ring‐Closing Metathesis.

M. Carda, J. Marco, S. Rodríguez, 2002 .

Synthesis of Conjugated γ- and δ-Lactones from Aldehydes and Ketones via a Vinylation/Allylation-Ring Closing Metathesis-Oxidation Sequence

M. Carda, S. Uriel, J. Marco, 1999 .

A formal synthesis of the syributins and secosyrins and a synthetic approach towards the syringolides

M. Carda, E. Falomir, J. Marco, 1998 .

Stereoselective synthesis of α-substituted serines from protected erythrulose oximes

M. Carda, J. Marco, J. Murga, 1998 .

AN EFFICIENT PREPARATION OF SILYLATED DERIVATIVES OF L-ERYTHRULOSE 3,4-O-ACETALS

M. Carda, E. Falomir, J. Marco, 1999 .

Stereoselective Indium‐Mediated Allylation of Erythrulose Derivatives in Aqueous Media.

M. Carda, J. Marco, J. Murga, 1998 .

Short, stereoselective synthesis of the naturally occurring pyrrolidine radicamine B and a formal synthesis of nectrisine.

M. Carda, E. Falomir, J. Marco, 2008, The Journal of organic chemistry.

Stereoselective anti aldol reactions of erythrulose derivatives. Functionalized chiral d3 and d4 synthons.

M. Carda, E. Falomir, J. Marco, 2004, The Journal of organic chemistry.

Double diastereoselection in aldol reactions mediated by dicyclohexylchloroborane between L-erythrulose derivatives and chiral aldehydes. The Felkin-Anh versus Cornforth dichotomy.

M. Carda, E. Falomir, J. Marco, 2003, The Journal of organic chemistry.

NEW OXYGENATED EUDESMANOLIDES FROM ARTEMISIA HERBA-ALBA

J. Lex, J. Marco, J. Jakupovic, 1990 .

Stereoselective synthesis of syn-α-methyl-β-hydroxy esters

M. Carda, E. Falomir, J. Marco, 2000 .

Chlorodicyclohexylborane-Mediated Aldol Additions of α,α‘-Dioxygenated Ketones

M. Carda, E. Falomir, J. Marco, 2001 .

Synthesis of Protected Enantiopure Erythrulose Derivatives

M. Carda, J. Marco, J. Murga, 1996 .

Highly diastereoselective additions of organometallic reagents to 1-O-silylated 3,4-Di-O-benzyl-L-erythrulose derivatives

M. Carda, J. Marco, F. González, 1993 .

Stereoselective synthesis of a C19–C26 fragment of amphidinolides G and H

M. Carda, P. Formentin, J. Marco, 2006 .

Aldol Reactions with Erythrulose Derivatives: Stereoselective Synthesis of Differentially Protected syn-α,β-Dihydroxy Esters

M. Carda, E. Falomir, J. Marco, 2000 .

Stereoselective synthesis of the naturally occurring styryllactones (+)-goniofufurone and (+)-cardiobutanolide.

M. Carda, J. Marco, J. Murga, 2005, The Journal of organic chemistry.

Further flavonol glycosides from Anthyllis onobrychioides

J. Marco, J. F. Sanz, O. Barberá, 1986 .

Sesquiterpene lactones from Artemisia herba-alba subsp. Herba-alba

J. Marco, 1989 .

Sesquiterpene lactones from Artemisia herba-alba

G. Castellano, J. Marco, J. F. Sanz, 1990 .

Sesquiterpene lactones and lignans from Centaurea species

F. Sancenón, A. Susanna, A. Rustaiyan, 1992 .

13C NMR spectra of eudesmane derivatives

M. Carda, J. Marco, J. F. Sanz, 1992 .

Sesquiterpene lactones fromArtemisia barrelieri

M. Carda, J. Marco, J. Jakupovic, 1991 .

Oxygenated nerolidol esters and eudesmane acids fromInula viscosa

J. Marco, J. F. Sanz, C. Ferrando, 1991 .

Sesquiterpene lactones, waxes and volatile compounds from Artemisia herba-alba subspecies Valentina

J. Marco, J. M. Sendra, E. Seoane, 1979 .

Flavonoids and other phenolics from Artemisia hispanica

J. Marco, S. Rodríguez, Concepción Domingo, 1988 .

3-Methoxyflavones and coumarins from Artemisia incanescens

J. Marco, J. F. Sanz, O. Barberá, 1986 .

A new flavonol diglycoside from Anthyllis onobrychioides

J. Marco, J. F. Sanz, O. Barberá, 1986 .

Flavonol glycosides from Anthyllis onobrychioides

J. Marco, J. F. Sanz, O. Barberá, 1985 .

Waxes, triterpenes and free acids in Anthyllis sericea

J. Marco, B. Abarca, J. M. Sendra, 1978 .

A Melampolide from Artemisia oliveriana

A. Rustaiyan, J. Marco, J. F. Sanz, 1990 .

Sesquiterpene lactones from Artemisia species

F. Sancenón, A. Rustaiyan, J. Marco, 1993 .

Sesquiterpene lactones from Artemisia caerulescens Subsp. gargantae

J. Marco, J. F. Sanz, 1990 .

Sesquiterpene lactones from Artemisia hispanica

J. Marco, J. F. Sanz, O. Barberá, 1989 .

Sesquiterpene lactones and dihydroflavonols from Andryala and Urospermum species

J. Marco, J. F. Sanz-Cervera, A. Yuste, 1994 .

Two eudesmane acids from Artemisia vulgaris

J. Marco, J. F. Sanz, P. D. Hierro, 1991 .

Phenolic constituents from Artemisia annua.

J. Marco, J. F. Sanz, O. Barberá, 1990 .

13C NMR spectra of eudesmanolides I—eudesman‐12,6‐olides

M. Carda, J. Marco, 1987 .

Further new sesquiterpene lactones from Artemisia herba-alba subsp. valentina.

J. Marco, J. F. Sanz, E. Falco, 1990 .

The Stereochemistry and Solid State Conformation of the Eudesmanolides Torrentin and 11-epi-Torrentin

J. Lex, M. Carda, J. Marco, 1992 .

Revision of the structure of torrentin

M. Carda, J. Marco, J. F. Sanz, 1989 .

Sesquiterpenes from Centaurea aspera.

F. Sancenón, M. Carda, J. Marco, 2005, Phytochemistry.

Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species

A. Susanna, N. Garcia‐Jacas, J. Marco, 1994 .

Nmr Studies of Tatridin A and Some Related Sesquiterpene Lactones from Tanacetum vulgare

J. Marco, J. F. Sanz, 1991 .

Sesquiterpene lactones from Artemisia inculta

J. Marco, M. Guara, J. F. Sanz-Cervera, 1997 .

Influence of conformational factors on acid‐catalyzed cyclizations of germacranolides: Molecular structure of the cyclization products of gallicin and 8α‐hydroxygallicin (shonachalin a)

L. Domingo, J. Lex, M. Carda, 1995 .

Sesquiterpene lactones from Picris echioides

M. Carda, J. Marco, J. F. Sanz, 1992 .

Total syntheses of rothin-A and rothin-B

M. Carda, J. Marco, M. Arnó, 1986 .

SESQUITERPENE LACTONES FROM NORTH AFRICAN ARTEMISIA SPECIES

F. Sancenón, J. Marco, J. F. Sanz-Cervera, 1994 .

Sesquiterpene lactones and lignans from Artemisia arborescens

J. Marco, J. F. Sanz-Cervera, Vicente García-Lliso, 1997 .

Sesquiterpene lactones from Artemisia lucentica

J. Marco, J. F. Sanz-Cervera, N. Batlle, 1997 .

Bisabolene derivatives and sesquiterpene lactones from Cousinia species

R. Albiach, Z. Habibi, A. Rustaiyan, 1993 .

Synthesis of umbellifolide and three natural eudesman-12,8-olides from (-)-artemisin

M. Carda, J. Marco, 1987 .

Germacranolides and a monoterpene cyclic peroxide from Artemisia fragrans

J. Marco, M. Guara, J. F. Sanz-Cervera, 1998 .

New germacranolides and eudesmanolides from North African Artemisia herba-alba

M. Carda, J. Marco, S. Rodríguez, 1994 .

Germacranolides and a Monoterpene Cyclic Peroxide from Artemisia fragrans.

J. Marco, M. Guara, J. F. Sanz-Cervera, 1998 .

Chlorinated thymol derivatives from Inula crithmoides

J. Marco, J. F. Sanz-Cervera, E. Manglano, 1993 .

Oxygenated germacranes from Santolina chamaecyparissus

J. Lex, M. Carda, J. Marco, 1993 .

New eudesmane derivatives from Artemisia tournefortiana

J. Marco, J. F. Sanz, 1990 .

New acetylenes from Chrysanthemum coronarium L.

J. Marco, J. F. Sanz, E. Falco, 1990 .

A sesquiterpene ester from Lactuca serriola

R. Albiach, J. Marco, J. F. Sanz, 1992 .

Sesquiterpene lactones and acetylenes from Artemisia reptans

F. Sancenón, J. Marco, M. Arnó, 1994 .

Synthesis of sinapyl alcohol diisovalerate, a new phenylpropanoid from Artemisia assoana.

J. Marco, J. F. Sanz, 1990 .

Synthesis of yomogin, 1-deoxyivangustin, and 1-deoxy-8-epiivangustin

M. Carda, J. Marco, M. Arnó, 1987 .

Oplopanone derivatives monoterpene glycosides from Artemisia sieberi

F. Sancenón, J. Marco, J. Jakupovic, 1993 .

Germacrane derivatives from Santolina chamaecyparissus

J. Marco, J. F. Sanz, Asunción Garcia-Sarrión, 1991 .

Absolute Configurations of Three Naturally Occurring Acetylenic Spiroacetal Enol Ethers

O. Hofer, J. Marco, G. Wurz, 1993 .

New umbelliferone sesquiterpene ethers from roots of Ligularia persica

A. Rustaiyan, J. Marco, J. F. Sanz, 1991 .

Neue eudesmane derivatives from Artemisia tournefortiana

J. Marco, J. F. Sanz, 1990 .

Triterpenes, Waxes and Tricin in Phoenix canariensis

J. Marco, A. Tortajada, B. García, 1981 .

A cadinane derivative from Artemisia crithmifolia

J. Marco, J. F. Sanz, Vicente García-Lliso, 1991 .

Tandem cycloaddition–enzymatic transesterification. An enantioselective Diels–Alder reaction equivalent

G. Asensio, J. Marco, C. Andreu, 1990 .

Total synthesis of the monoterpenes (−)-mintlactone and (+)-isomintlactone

M. Carda, J. Marco, 1992 .

Total synthesis of (−)-mintlactone

M. Carda, J. Marco, 1991 .

Waxes and volatile oils inHypericum ericoides (Guttiferae)

J. Marco, M. L. Cardona, J. M. Sendra, 1983, Lipids.

Tandem Cycloaddition-Enzymatic Transesterification. An Enantioselective Diels-Alder Reaction Equivalent.

G. Asensio, J. Marco, C. Andreu, 1991 .

Total Synthesis of the Monoterpenes (-)-Mintlactone and (+)- Isomintlactone.

M. Carda, J. Marco, 1993 .

Total Synthesis of (‐)‐Mintlactone (I).

M. Carda, J. Marco, 1992 .

Enantioselective synthesis and absolute configurations of aculeatins A, B, D, and 6-epi-aculeatin D

M. Carda, E. Falomir, J. Marco, 2006 .

Enantioselective synthesis and absolute configurations of aculeatins A and B

M. Carda, E. Falomir, J. Marco, 2005 .

A novel germacranolide-aminoacid adduct dimer from centaurea aspera

J. Marco, J. Jakupovic, J. F. Sanz, 1991 .

Stereoselective synthesis of anamarine

M. Carda, E. Falomir, J. Marco, 2004 .

Synthesis of honokiol analogues and evaluation of their modulating action on VEGF protein secretion and telomerase‐related gene expressions

M. Carda, E. Falomir, J. Marco, 2017, Chemical biology & drug design.

Synthesis of combretastatin A-4 O-alkyl derivatives and evaluation of their cytotoxic, antiangiogenic and antitelomerase activity.

M. Carda, E. Falomir, S. Torijano-Gutiérrez, 2013, Bioorganic & medicinal chemistry.

Biomimetic Diels−Alder Cyclizations for the Construction of the Brevianamide, Paraherquamide Sclerotamide, and VM55599 Ring Systems

F. Sancenón, J. Marco, Robin M. Williams, 1998 .

Stereoselective synthesis of the bacterial DNA primase inhibitor Sch 642305 and its C-4 epimer

M. Carda, J. Marco, J. García-Fortanet, 2007 .

Synthesis of Combretastatin A-4 and 3′-Aminocombretastatin A-4 derivatives with Aminoacid Containing Pendants and Study of their Interaction with Tubulin and as Downregulators of the VEGF, hTERT and c-Myc Gene Expression

M. Carda, Raül Agut, E. Falomir, 2020, Molecules.

Synthesis and biological evaluation as antiangiogenic agents of ureas derived from 3'-aminocombretastatin A-4.

M. Carda, E. Falomir, J. Marco, 2019, European journal of medicinal chemistry.

Inhibitory effect of cytotoxic stilbenes related to resveratrol on the expression of the VEGF, hTERT and c-Myc genes.

M. Carda, R. Martí-Centelles, E. Falomir, 2015, European journal of medicinal chemistry.

Inhibitory effect of cytotoxic nitrogen-containing heterocyclic stilbene analogues on VEGF protein secretion and VEGF, hTERT and c-Myc gene expression

M. Carda, R. Martí-Centelles, E. Falomir, 2015 .

Arylureas derived from colchicine: Enhancement of colchicine oncogene downregulation activity.

M. Carda, E. Falomir, J. Marco, 2018, European journal of medicinal chemistry.

Inhibitory effect of pironetin analogue/colchicine hybrids on the expression of the VEGF, hTERT and c-Myc genes.

M. Carda, E. Falomir, J. Marco, 2015, Bioorganic & medicinal chemistry letters.

A germacrane derivative from Pallenis spinosa

J. Marco, J. F. Sanz, 1991 .

Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis

J. Marco, J. F. Sanz-Cervera, A. Yuste, 1997 .

Stereoselective synthesis of the cytotoxic 14-membered macrolide aspergillide A.

M. Carda, J. Marco, J. Murga, 2010, The Journal of organic chemistry.

Biomimetic Diels-Alder cyclizations for the construction of the brevianamide, paraherquamide, sclerotamide, asperparaline and VM55599 ring systems.

F. Sancenón, R. Williams, J. Marco, 1998, Bioorganic & medicinal chemistry.

BIOSYNTHESIS OF THE BREVIANAMIDES. AN AB INITIO STUDY OF THE BIOSYNTHETIC INTRAMOLECULAR DIELS-ALDER CYCLOADDITION

Robert M. Williams, L. Domingo, J. Marco, 1997 .

Caryophyllene derivatives from Pulicaria dysenterica

R. Albiach, J. Marco, J. F. Sanz, 1992 .

Germacrane esters from roots of Ligularia persica

A. Rustaiyan, J. Marco, J. F. Sanz, 1991 .

Diastereoselectivity in Organometallic Additions to the Carbonyl Group of Protected Erythrulose Derivatives.

M. Carda, J. Marco, J. Murga, 1998, The Journal of organic chemistry.

Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine

M. Carda, E. Falomir, J. Marco, 2008 .

Novel multitarget inhibitors with antiangiogenic and immunomodulator properties.

M. Carda, E. Falomir, J. Marco, 2019, European journal of medicinal chemistry.

Effects on tubulin polymerization and down-regulation of c-Myc, hTERT and VEGF genes by colchicine haloacetyl and haloaroyl derivatives.

M. Carda, E. Falomir, J. Marco, 2018, European journal of medicinal chemistry.

Stereoselective synthesis of ent-communiols A-C

M. Carda, E. Falomir, J. Marco, 2005 .

Stereoselective Synthesis of ent-Communiols A—C.

M. Carda, J. Marco, J. Murga, 2006 .

Jatrophane and tigliane diterpenes from the latex of Euphorbia obtusifolia

E. Palomares, J. Marco, B. Fraga, 1999 .

Tigliane diterpenes from the latex of Euphorbia obtusifolia with inhibitory activity on the mammalian mitochondrial respiratory chain.

E. Palomares, J. Marco, E. Estornell, 2003, Journal of ethnopharmacology.

Jatrophane Diterpenes from the Latex of Euphorbia obtusifolia with Inhibitory Activity on the Mammalian Mitochondrial Respiratory Chain

J. Marco, E. Estornell, L. Betancur-Galvis, 2003, Planta medica.

Terracinolides from Euphorbia terracina

J. Marco, J. Jakupovic, J. F. Sanz-Cervera, 1997 .

N-alpha-Aminoacyl Colchicines as Promising Anticancer Agents.

S. Noppen, S. Liekens, M. Carda, 2019, Medicinal chemistry (Shariqah (United Arab Emirates)).

A New Butenolide from Conyza bonariensis.

J. Marco, J. Sanz, 1991 .

Stereoselective total synthesis and absolute configuration of the natural decanolides (-)-microcarpalide and (+)-lethaloxin. Identity of (+)-lethaloxin and (+)-pinolidoxin.

M. Carda, E. Falomir, J. Marco, 2005, The Journal of organic chemistry.

A formal, stereoselective synthesis of the natural tetrahydropyran derivative ophiocerin D

M. Carda, E. Falomir, J. Marco, 2010 .

Stereoselective synthesis of the published structure of feigrisolide A. Structural revision of feigrisolides A and B.

M. Carda, J. Marco, J. Murga, 2006, The Journal of organic chemistry.

Synthesis of N-acyl Derivatives of Aminocombretastatin A-4 and Study of their Interaction with Tubulin and downregulation of c-Myc.

M. Carda, Raül Agut, E. Falomir, 2020, Medicinal chemistry.

The stereochemistry and solid state conformation of 1,10β-epoxyachillin

J. Lex, J. Marco, O. Barberá, 1989 .

Stereoselective synthesis and structural correction of the naturally occurring lactone stagonolide G.

M. Carda, J. Marco, J. Murga, 2010, Organic letters.