المؤلفون: Thomas J. Struble (6007892), Ivor Smajlagic (5905877), Hayden Foy (5647226), Travis Dudding (1334103), Jeffrey N. Johnston (1321833)

مصطلحات موضوعية: Biophysics, Biochemistry, Pharmacology, Biotechnology, Immunology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, supports distinct models, nonsymmetric congener exhibits, favorable dispersion forces, detailed computational analysis, catalyst )- controlled, bifunctional brønsted acid, based stereochemical rationales, hindered binding cavity, henry reactions leading, enantioselective direct aza, henry reactions, enantioselective aza, enantioselective catalysis, wide range, ultimately favoring, syn <, selectivity resulting, pre -<, nitronate activation, highly diastereo, first time, diamino esters, c <

Relation: https://figshare.com/articles/journal_contribution/DFT-Based_Stereochemical_Rationales_for_the_Bifunctional_Br_nsted_Acid_Base-Catalyzed_Diastereodivergent_and_Enantioselective_aza-Henry_Reactions_of_Nitro_Esters/16840087

الاتاحة: https://doi.org/10.1021/acs.joc.1c02112.s001