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Randolph Alonso

Synthesis of Conformationally Restricted Carbocyclic Nucleosides: The Role of the O(4′)-Atom in the Key Hydration Step of Adenosine Deaminase
1999 · Victor E. Marquez, Pamela Russ, et al. · Helvetica Chimica Acta · 77
Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14-labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol
2003 · José Villamizar, Juan Fuentes, et al. · Journal of Natural Products · 37
Conformationally Restricted Nucleosides. The Reaction of Adenosine Deaminase with Substrates Built on a Bicyclo[3.1.0]hexane Template
1999 · Victor E. Marquez, Pamela Russ, et al. · Nucleosides and Nucleotides · 30
An Efficient Method for the Synthesis of (+)-Cyclozonarone, Isozonarol Δ,8,9and Isozonarone Δ8,9
2003 · José Villamizar, Juan Fuentes, et al. · Synthetic Communications · 13
Highly efficient Synthesis of the Optically Active Sesquiterpene Hydroquinone (+)-Zonarol and the Sesquiterpene Quinone (+)-Zonarone
2002 · José Villamizar, Angel L. Orcajo, et al. · Journal of Chemical Research · 11
Cytostatic and Cytotoxic Activity of Synthetic Diterpene Derivatives Obtained from (-)-Kaur-9(11), 16-Dien-19-Oic Acid Against Human Cancer Cell Lines
2005 · Randolph Alonso, Heidi Gomis, et al. · Letters in Drug Design & Discovery · 10
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
1998 · Tatsuhiko Nakano, Randolph Alonso, et al. · Journal of the Chemical Society Perkin Transactions 1 · 9
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
1995 · Tatsuhiko Nakano, Randolph Alonso, et al. · Tetrahedron Letters · 7
Synthesis of (+)-Coronarin E, (-)-7- epi -Coronarin a and (+)-15, 16-Epoxy-8(17), 13(16), 14-Labdatriene from (+)-Manool
2003 · José Villamizar, Franklin Salazar, et al. · Journal of Chemical Research · 5
Synthetic diterpene derivatives from kaura-9(11),16-dien-19-oic acid: Cytostatic and cytotoxic activity against human cancer cell lines
2006 · R. Alonso · Pharmaceutical Chemistry Journal · 3
Synthesis of Trinorditerpenoid Derivatives and Evaluation of Antimicrobial and Cytotoxic Activity
2005 · R. Alonso, H. Gomis, et al. · Chemistry of Natural Compounds · 1
Untitled
1999 · Victor E. Marquez, Pamela Russ, et al. · Helvetica Chimica Acta · 1
Synthesis of (+)‐Coronarin E, (‐)‐7‐epi‐Coronarin A and (+)‐15, 16‐Epoxy‐8(17), 13(16), 14‐Labdatriene from (+)‐Manool.
2004 · Jose Villamizar, Franklin Salazar, et al. · ChemInform
An Efficient Method for the Synthesis of (+)‐Cyclozonarone, Isozonarol Δ8,9 and Isozonarone Δ8,9.
2003 · Jose Villamizar, Juan Fuentes, et al. · ChemInform
Highly Efficient Synthesis of the Optically Active Sesquiterpene Hydroquinone (+)‐Zonarol and the Sesquiterpene Quinone (+)‐Zonarone.
2003 · Jose Villamizar, Angel L. Orcajo, et al. · ChemInform
ChemInform Abstract: Synthesis of Conformationally Restricted Carbocyclic Nucleosides: The Role of the O(4′)‐Atom in the Key Hydration Step of Adenosine Deaminase.
2000 · Victor E. Marquez, Pamela Russ, et al. · ChemInform
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.
1998 · T. NAKANO, R. ALONSO, et al. · ChemInform
A concise approach to the antiviral nucleoside (1R,2S,4S,5S)-1-hydroxymethyl-2-hydroxy-4-(6-amino-9-purinyl)bicyclo[3.1.0]hexane
1998 · Víctor E. Márquez, 신계정, et al.
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.
1995 · T. NAKANO, R. ALONSO, et al. · ChemInform
Works count: 19
Citation count: 204
H-index: 7
I10-index: 6
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