000107379 001__ 107379
000107379 005__ 20220511133123.0
000107379 0247_ $$2doi$$a10.1002/adsc.202000848
000107379 0248_ $$2sideral$$a120996
000107379 037__ $$aART-2020-120996
000107379 041__ $$aeng
000107379 100__ $$0(orcid)0000-0002-3726-0493$$aAuria-Luna, F.
000107379 245__ $$aAsymmetric Fluorination Reactions promoted by Chiral Hydrogen Bonding-based Organocatalysts
000107379 260__ $$c2020
000107379 5060_ $$aAccess copy available to the general public$$fUnrestricted
000107379 5203_ $$aFluorinated compounds can exhibit interesting biological properties. The importance of these species has made that the chemistry of fluorine has experienced a great development. On this review, the recent advances on asymmetric fluorination reactions promoted by chiral hydrogen bonding-based organocatalysts are discussed. Hence, examples using phosphoric acid, carboxylic acid, (thio)urea and squaramide derivatives are illustrated. The growth of this field is amazing. We have only considered pivotal works in which direct fluorination takes place using a fluorinating agent, leaving aside the reactions where a fluorine atom is incorporated from the beginning as part of other reactants. Herein, the scarce existing examples on this field of research have been compiled.
000107379 536__ $$9info:eu-repo/grantAgreement/ES/DGA-FSE/E07-20R$$9info:eu-repo/grantAgreement/ES/MINECO-FEDER/CTQ2016-75816-C2-1-P$$9info:eu-repo/grantAgreement/ES/MINECO-FEDER/CTQ2017-88091-P$$9info:eu-repo/grantAgreement/ES/MINECO/PID2019-104379RB-C21
000107379 540__ $$9info:eu-repo/semantics/openAccess$$aAll rights reserved$$uhttp://www.europeana.eu/rights/rr-f/
000107379 590__ $$a5.837$$b2020
000107379 591__ $$aCHEMISTRY, ORGANIC$$b7 / 57 = 0.123$$c2020$$dQ1$$eT1
000107379 591__ $$aCHEMISTRY, APPLIED$$b11 / 74 = 0.149$$c2020$$dQ1$$eT1
000107379 592__ $$a1.54$$b2020
000107379 593__ $$aOrganic Chemistry$$c2020$$dQ1
000107379 593__ $$aCatalysis$$c2020$$dQ1
000107379 655_4 $$ainfo:eu-repo/semantics/article$$vinfo:eu-repo/semantics/acceptedVersion
000107379 700__ $$aMohammadi, S.
000107379 700__ $$aDivar, M.
000107379 700__ $$0(orcid)0000-0003-0553-0695$$aGimeno, M.C.$$uUniversidad de Zaragoza
000107379 700__ $$0(orcid)0000-0002-5244-9569$$aPerez Herrera, R.$$uUniversidad de Zaragoza
000107379 7102_ $$12010$$2760$$aUniversidad de Zaragoza$$bDpto. Química Inorgánica$$cÁrea Química Inorgánica
000107379 7102_ $$12013$$2765$$aUniversidad de Zaragoza$$bDpto. Química Orgánica$$cÁrea Química Orgánica
000107379 773__ $$g362, 23 (2020), 5275-5300$$pAdv. synth. catal.$$tAdvanced Synthesis and Catalysis$$x1615-4150
000107379 8564_ $$s2775745$$uhttps://zaguan.unizar.es/record/107379/files/texto_completo.pdf$$yPostprint
000107379 8564_ $$s719142$$uhttps://zaguan.unizar.es/record/107379/files/texto_completo.jpg?subformat=icon$$xicon$$yPostprint
000107379 909CO $$ooai:zaguan.unizar.es:107379$$particulos$$pdriver
000107379 951__ $$a2022-05-11-13:13:22
000107379 980__ $$aARTICLE