C
Carlos Cativiela
Researcher at University of Zaragoza
Publications - 350
Citations - 5791
Carlos Cativiela is an academic researcher from University of Zaragoza. The author has contributed to research in topics: Enantioselective synthesis & Amino acid. The author has an hindex of 36, co-authored 350 publications receiving 5425 citations. Previous affiliations of Carlos Cativiela include University of Barcelona & Complutense University of Madrid.
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Journal ArticleDOI
Diversity and Hierarchy in Supramolecular Assemblies of Triphenylalanine: From Laminated Helical Ribbons to Toroids
Enric Mayans,Jordi Casanovas,Ana M. Gil,Ana I. Jiménez,Carlos Cativiela,Jordi Puiggalí,Carlos Alemán +6 more
TL;DR: It is demonstrated that FFF assemblies can organize in a wide number of well-defined supramolecular structures, which include laminated helical-ribbons, leaflike dendrimers, doughnut-, needle-, and flower-shapes.
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Cyclopalladation and reactivity of amino esters through C-H bond activation: experimental, kinetic, and density functional theory mechanistic studies.
Eduardo Laga,Angel García-Montero,Francisco J. Sayago,Tatiana Soler,Salvador Moncho,Carlos Cativiela,Manuel Martínez,Esteban P. Urriolabeitia +7 more
TL;DR: The experimental observations indicated an improvement in the yields of the orthopalladated compounds when the N-amine and/or the C-α atom are substituted, when compared with the unsubstituted methyl phenylglycinate derivatives.
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A straightforward synthesis of both enantiomers of α-vinylalanine and α-ethynylalanine
TL;DR: In this article, the synthesis of enantiomerically pure (S )- and ( R )-α-vinylalanines and ( S )-and ( R ε)-α-ethynylalanine, four quaternary α-amino acids, using a straightforward synthetic route and starting from (S ǫ)- and (R )- N -Boc-N,O -isopropylidene-α -methyl serinals.
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Dynamic kinetic resolution of 1,3-dihydro-2H-isoindole-1-carboxylic acid methyl ester: asymmetric transformations toward isoindoline carbamates.
Roberto Morán-Ramallal,Vicente Gotor-Fernández,Pedro Laborda,Francisco J. Sayago,Carlos Cativiela,Vicente Gotor +5 more
TL;DR: Optically active carbamates were obtained in good yields and an excellent degree of stereoselectivity when Pseudomonas cepacia lipase was used as biocatalyst, with diallyl or dibenzyl carbonates being both adequate reagents in alkoxycarbonylation reactions.
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Stereoselective synthesis of acyclic α,α-disubstituted α-amino acids derivatives from amino acids templates
TL;DR: The most important and available references have been collected in this article to prove the versatility of stereoselective synthesis of acyclic α,α-disubstituted α-amino acids from amino acids template equivalents.