Organocatalytic Asymmetric Vinylogous Michael Addition of Dicyanoolefins to Imine Intermediates Generated in situ from Arenesulfonylalkylindoles - Zhu, Xing-Li; He, Wu-Jun; Yu, Liang-Liang; Cai, Chang-Wu; Zuo, Zong-Le; Qin, Da-Bin; Liu, Quan-Zhong; Jing, Lin-Hai (Advanced synthesis & catalysis, 2012)
Keywords: Adducts; arenesulfonylalkylindoles; asymmetric catalysis; Asymmetry; Catalysis; Catalysts: preparations and properties; Chemistry; Chemistry, Applied; Chemistry, Organic; Derivatives; dicyanoolefins; Exact sciences and technology; General and physical chemistry; Heterocyclic compounds; Heterocyclic compounds with only one n hetero atom and condensed derivatives; Imines; Indoles; Ketones; Michael reaction; organic catalysis; Organic chemistry; Physical Sciences; Preparations and properties; Science & Technology; Synthesis; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; vinylogous Michael addition; dicyanoolefins; ENANTIOSELECTIVE SYNTHESIS; NATURAL-PRODUCTS; BETA-SUBSTITUTED TRYPTOPHANS; 3-(1-ARYLSULFONYLALKYL) INDOLES; ALDOL REACTIONS; arenesulfonylalkylindoles; asymmetric catalysis; CARBON BOND FORMATION; ALPHA-AMIDO SULFONES; MANNICH REACTION; organic catalysis; vinylogous Michael addition; ARYLSULFONYL INDOLES; FRIEDEL-CRAFTS ALKYLATION; Michael addition; Catalytic reaction; Enantioselectivity; Nitrogen heterocycle; Organocatalyst; Imine; Asymmetric catalysis; Ketone; Alkylation; Diastereoselectivity; Asymmetric synthesis; Vinylic compound; Enantiomeric excess; Indole derivatives