Highly Stereoselective Synthesis of trans-Dihydronarciclasine Analogues

Highly Stereoselective Synthesis of trans-Dihydronarciclasine Analogues Stereoselective synthesis of trans-dihydronarciclasine derivatives containing a 1,4-benzodioxane moiety Stereoselective Synthesis of Novel (±)-trans-Dihydronarciclasine Analogues: Preparation of a Pivotal Intermediate Containing Two Methoxy Substituents Controlling stereoselectivity by enzymatic and chemical means to access enantiomerically pure (1S,3R)-1-benzyl-2,3-dimethyl-1,2,3,4-tetrahydroisoquinoline derivatives Synthesis and AChE inhibitory activity of new chiral tetrahydroacridine analogues from terpenic cyclanones Highly Enantioselective and Practical Cinchona-Derived Phase-Transfer Catalysts for the Synthesis of α-Amino Acids This work was supported by grants from Aminogen Co. (Korea) through the Research Center of New Drug Development of Seoul National University and the Research Institute of Pharmaceutical Sciences in the College of Pharmacy of Seoul National University. (±)-trans-Dihydronarciclasine and (±)-trans-dihydrolycoricidine analogues modified in their ring A: Evaluation of their anticancer activity and a SAR study Non‐Biaryl Atropisomers in Organocatalysis Asymmetric Synthesis of (-)-Indolizidine167B and (+)-Coniine Enantioselective desymmetrisation of an epoxytropinone for peduncularine synthesis