Jing, Kun Wang, Xiang-Nan Wang, Guan-Wu Diastereoselective Synthesis of Oxazoloisoindolinones via Cascade Pd-Catalyzed <i>ortho</i>-Acylation of <i>N</i>‑Benzoyl α‑Amino Acid Derivatives and Subsequent Double Intramolecular Cyclizations The first cascade diastereoselective synthesis of oxazoloisoindolinones via the palladium-catalyzed decarboxylative <i>ortho</i>-acylation of <i>N</i>-benzoyl α-amino acid derivatives followed by double intramolecular cyclizations has been demonstrated. This reaction, using α-amino acids as directing groups and α-oxocarboxylic acids as the acylation source, features a broad substrate scope, good functional group tolerance, high regioselectivity, and excellent diastereoselectivity. intramolecular cyclizations;Subsequent Double Intramolecular Cyclizations;Diastereoselective Synthesis;Cascade Pd-Catalyzed ortho;palladium-catalyzed decarboxylative ortho;acylation source;cascade diastereoselective synthesis;acid derivatives;benzoyl α-;group tolerance;substrate scope;α- oxocarboxylic acids 2018-12-04
    https://acs.figshare.com/articles/dataset/Diastereoselective_Synthesis_of_Oxazoloisoindolinones_via_Cascade_Pd-Catalyzed_i_ortho_i_-Acylation_of_i_N_i_Benzoyl_Amino_Acid_Derivatives_and_Subsequent_Double_Intramolecular_Cyclizations/7473281
10.1021/acs.joc.8b02509.s002