10b-Substituted hexahydropyrrolo-isoquinolines: studies on diastereoselective formation of a quaternary carbon stereocenter via N-acyliminium ion cyclization
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference33 articles.
1. New Developments in the Chemistry of N-Acyliminium Ions and Related Intermediates
2. Chiral Heterocycles by Iminium Ion Cyclization
3. The Isoquinoline Alkaloids;Bentley,1998
4. Asymmetric Synthesis of Isoquinoline Alkaloids
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1. Synthesis of Hexahydropyrrolo-isoquinolines by 1,3-Dipolar cycloaddition of tetrahydroisoquinolines and cinnamaldehydes;Tetrahedron Letters;2023-06
2. cis-Dihydroxylated α-Trifluoromethylated N,O-Acetal from l-Tartaric Acid: Synthesis of Tetrasubstituted Stereocenter via Diastereoselective Pictet-Spengler Cyclization of N-Acyliminium Ions;The Journal of Organic Chemistry;2020-07-27
3. Diastereoselective Ritter-like Reaction on Cyclic Trifluoromethylated N,O-Acetals Derived from l-Tartaric Acid;The Journal of Organic Chemistry;2017-09-08
4. Synthesis and antimicrobial activity of chiral quaternary N-spiro ammonium bromides with 3',4'-dihydro-1'H-spiro[isoindoline-2,2'-isoquinoline] skeleton;Drug Design, Development and Therapy;2017-07
5. Biological evaluation of octahydropyrazin[2,1-a:5,4-a′]diisoquinoline derivatives as potent anticancer agents;Tumor Biology;2017-06
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