Controlling stereoselectivity by enzymatic and chemical means to access enantiomerically pure (1S,3R)-1-benzyl-2,3-dimethyl-1,2,3,4-tetrahydroisoquinoline derivatives

Controlling stereoselectivity by enzymatic and chemical means to access enantiomerically pure (1S,3R)-1-benzyl-2,3-dimethyl-1,2,3,4-tetrahydroisoquinoline derivatives Asymmetric Construction of Alkaloids by Employing a Key ω‐Transaminase Cascade Enantiodivergent Synthesis of 1-Heteroaryl Tetrahydroisoquinolines Catalyzed by Imine Reductases Synthesis of an advanced precursor of Rivastigmine: Cinchona -derived quaternary ammonium salts as organocatalysts for stereoselective imine reductions Chemoenzymatic Enantioselective Synthesis of the Hancock Alkaloids (S)- and (R)-Galipeine, (S)-Cuspareine, (S)-Galipinine, and (S)-Angustureine Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloids Two‐Step Catalytic Transformation ofN‐Benzyllactams to Alkaloids (±)‐Solenopsin, (±)‐Solenopsin A, and (+)‐Julifloridine Asymmetric Synthesis of (-)-Indolizidine167B and (+)-Coniine Synthesis of C3/C1-Substituted Tetrahydroisoquinolines Stereoselective synthesis of trans-dihydronarciclasine derivatives containing a 1,4-benzodioxane moiety