1. Digitum: Repositorio Institucional de la Universidad de Murcia

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OM 21-539.pdf.jpg-22-feb-2021Sequential Insertion of Alkynes, Alkenes, and CO into the Pd-C Bond of ortho-Palladated Primary Phenethylamines: from Allyl Complexes and Enlarged Palladacycles to Functionalized Arylalkylamines
Organometallics 2012-3647rev.pdf.jpg14-may-2012-Ortho Palladation of the Phenethylamines of Biological Relevance L-Tyrosine Methyl Ester and Homoveratrylamine. Reactivity of the Palladacycles toward CO and Isocyanides. Synthesis of the Natural Alkaloid Corydaldine
REVISED VERSION-CHEMCOMMUN-2017-53-2842.pdf.jpg10-feb-20172017Synthesis of spiro-oxoindoles through Pd-catalyzed remote C–H alkylation using alpha-diazocarbonyl compounds
OM 12-8333rev.pdf.jpg10-dic-20122012Insertion of Allenes into the Pd-C bond of Ortho-Palladated Primary Arylamines of Biological Relevance: Phenethylamine, Phentermine, (L)-Phenylalanine Methyl Ester and (L)-Tryptophan Methyl Ester. Synthesis of 3-Benzazepines and Their Salts
OM-2017-4465.pdf.jpg14-nov-20172017Synthesis and Reactivity of Model Intermediates Proposed for the Pd-Catalyzed Remote C−H Functionalization of N‐(2- Haloaryl)acrylamides
OM-2010-4320.pdf.jpg13-sep-20102010Eight-membered Palladacycles Derived from the Insertion of Olefines into the Pd–C Bond of Ortho-palladated Pharmaceuticals Phenethylamine and Phentermine. Synthesis of Stable Heck-type Intermediates Containing Accessible β-Hydrogens and its Use in the Synthesis of 2-Styryl-phenethylamines, Tetrahydroisoquinolines and Eight-membered Cyclic Amidines
OM-2012-6351.pdf.jpg16-ago-20122012Reactivity toward CO of Eight-Membered Palladacycles Derived from the Insertion of Alkenes into the Pd–C Bond of Cyclopalladated Primary Arylalkylamines of Pharmaceutical Interest. Synthesis of Tetrahydrobenzazocinones, Ortho-Functionalized Phenethylamines, Ureas, and an Isocyanate
OM-2011-4624.pdf.jpg28-jul-20112011A New Method for High Yield Cyclopalladation of Primary and Secondary Amines. Atom-Efficient Open-to-Air Inexpensive Synthesis of Buchwald-Type Precatalysts
CHEM COMMUN-2012-6744.pdf.jpg16-may-20122012Insertion of benzyne into the Pd–C bond. Synthesis of unnatural amino acid derivatives by sequential insertion of benzyne and CO: 2,2’-functionalized biaryls containing alkylamino and carboxymethyl substituents. Isolation of stable carbopalladated-benzyne intermediates

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