A. MARTIN

Instituto de Ciencia y Tecnología de Polímeros — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

7h-index142citations35works0.02yr avg
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Research Topics

Biological Activity of Diterpenoids and Biflavonoids(10), Oxidative Organic Chemistry Reactions(8), Marine Sponges and Natural Products(7), Synthetic Organic Chemistry Methods(7), Photochemistry and Electron Transfer Studies(4)

Publications35 total

Synthesis, characterization and controlled release behaviour of adducts from chloroacetylated cellulose and α-naphthylacetic acid
Reactive and Functional Polymers·1999· 33 cited
ChemInform Abstract: Facile Access to Optically Active Ring C Aromatic Diterpene Derivatives from Manool. Highly Efficient Syntheses of (+)‐12‐Methyl‐7‐oxopodocarpa‐8,11,13‐triene‐13‐carboxylic Acid, (+)‐13‐Methyl‐7‐oxopodocarpa‐8,11,13‐triene‐12‐carboxylic Acid and (+)‐Nimbiol.
ChemInform·1998
An Efficient Method for the Synthesis of Methyl 12α-Hydroxy-Isocopal-13(14)-En-15-Oate, a Key Precursor to a Variety of Sesterterpene Marine Sponge Metabolites
Natural product letters·1998
Facile access to optically active ring C aromatic diterpene derivatives from manool. Highly efficient syntheses of (+)-12-methyl-7-oxo-podocarpa-8,11,13-triene-13-carboxylic acid, (+)-13-methyl-7-oxopodocarpa-8,11,13-triene-12-carboxylic acid and (+)-nimbiol
Journal of the Chemical Society Perkin Transactions 1·1998· 9 cited
ChemInform Abstract: A Facile Access to Optically Active Ring C Aromatic Diterpene Derivatives. Highly Efficient Synthesis of (+)‐12‐Methyl‐7‐ oxopodocarpa‐8,11,13‐triene‐13‐carboxylic Acid and (+)‐13‐Methyl‐7‐ oxopodocarpa‐8,11,13‐triene‐12‐carboxylic Acid from Manool.
ChemInform·1995
A facile access to optically active ring C aromatic diterpene derivatives. Highly efficient synthesis of (+)-12-methyl-7-oxopodocarpa-8,11,13-triene-13-carboxylic acid and (+)-13-methyl-7-oxopodocarpa-8,11,13-triene-12-carboxylic acid from manool
Tetrahedron Letters·1995· 7 cited
Molecular rearrangements in derivatives of grandiflorenic acid [(-)-kaur-9(11),16-dien-19-oic acid]
Pure and Applied Chemistry·1994· 6 citedOpen Access
ChemInform Abstract: Buxus Alkaloids. Part 11. The Synthesis of Cycloprotobuxine‐A (3β, 20S‐Chirality) and Its Two Isomeric Alkaloids with 3β,20R‐ an 3. alpha.,20R‐ Configuration from Lanosterol.
ChemInform·1991
Buxus alkaloiks. Part XI. The synthesis of cycloprotobuxine-A (3β,20S-chirality) and its two isomeric alkaloids with 3β,20R- and 3α,20R- configuration from lanosterol.
Tetrahedron·1991· 1 cited
ChemInform Abstract: A Very Short, Highly Efficient Synthesis of Natural (‐)‐Warburganal.
ChemInform·1989
ChemInform Abstract: Total Syntheses of Marine Sponge Metabolites. Part 3. Stereoselective Total Synthesis of (.+‐.)‐12‐Deoxyscalaradial.
ChemInform·1988
Total syntheses of marine sponge metabolites. Part 3. Stereoselective total synthesis of (±)-12-deoxyscalaradial
Journal of the Chemical Society Perkin Transactions 1·1988· 14 cited
Kinetics and mechanism of elimination of methoxyphenethyl chlorides in the gas phase
Reaction Kinetics and Catalysis Letters·1987· 7 cited
ChemInform Abstract: Studies on Rearrangements in Derivatives of Grandiflorenic Acid.
Chemischer Informationsdienst·1986
Studies on Rearrangements in Derivatives of Grandiflorenic Acid, Part 2. Synthesis of Methyl (-)-20-Norkaur-9α-Methyl-5(10), 16-Dien-19-Oate, A New Tetracyclic Rosane-Type Diterpene
Journal of Natural Products·1986· 5 cited
ChemInform Abstract: Studies on Rearrangements in Derivatives of Grandiflorenic Acid. Part 1. Reaction of the Epoxides of Methyl (‐)‐Kaur‐9(11)‐en‐19‐oate and (‐)‐Kaur‐9(11)‐en‐19‐oic Acid with Boron Trifluoride‐Diethyl Ether Either in the Absence or in the Presence of N‐Nitrosomethylurea. Formation of Two Diterpenes of a New Skeletal Type.
Chemischer Informationsdienst·1985
Studies on rearrangements in derivatives of grandiflorenic acid. Part 1. Reaction of the epoxides of methyl (–)-kaur-9(11)-en-19-oate and (–)-kaur-9(11)-en-19-oic acid with boron trifluoride-diethyl ether either in the absence or in the presence of N-nitrosomethylurea. Formation of two diterpenes of a new skeletal type
Journal of the Chemical Society Perkin Transactions 1·1985· 6 cited
ChemInform Abstract: TOTAL SYNTHESES OF MARINE SPONGE METABOLITES. PART 2. SYNTHESIS OF (.+‐.)‐ENT‐ISOCOPAL‐12‐ENE‐15,16‐DIAL, (.+‐.)‐14‐EPI‐ENT‐ISOCOPAL‐12‐ENE‐15,16‐DIAL, AND (.+‐.)‐15‐ACETOXY‐ENT‐ISOCOPAL‐12‐EN‐16‐AL
Chemischer Informationsdienst·1984
ChemInform Abstract: Synthesis of Sugar Modified Daunorubicin Analogs; Approaches to Aclacinomycin Analogs (53 Literaturangaben).
Chemischer Informationsdienst·1983
ChemInform Abstract: SYNTHESIS OF LABDA‐8(17),13(14)‐DIEN‐15,16‐OLIDE AND 15,16‐EPOXYLABDA‐8(17),13(16),14‐TRIENE AND THEIR REARRANGEMENTS TO CLERODANE DERIVATIVES
Chemischer Informationsdienst·1982
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Frequent Co-authors

T. Nakano(14), Tatsuhiko Nakano(12), Alfredo Usubillaga(8), María Aracelis Maillo(6), J. D. Medina(4), Aníbal Rojas(4), Randolph Alonso(4), R. A. NUNEZ(4), Antonieta Castaldi Spinelli(4), Miguel A. Alonso(4), María Isabel Martín Hernández(3), Andrew T. McPhail(3), Kay D. Onan(3), Carlos Rivas(2), Concepción Pérez(2), Alberto Haces(2), Manuel Sánchez‐Chaves(1), Félix Arranz(1), A. Muñoz‐Escalona(1), José Miguel Hidalgo Herrador(1)