Chiral Amino Alcohols As Intermediates in the Stereocontrolled Synthesis of 1,3-Disubstituted Tetrahydroisoquinolines and Protoberberines
Author:
Affiliation:
1. Departamento de Química Orgánica, Facultad de Ciencias, Universidad del País Vasco, Apdo. 644-48080 Bilbao, Spain
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo981326h
Reference28 articles.
1. Synthesis and Molecular Modeling of 1-Phenyl-1,2,3,4-tetrahydroisoquinolines and Related 5,6,8,9-Tetrahydro-13bH-dibenzo[a,h]quinolizines as D1 Dopamine Antagonists
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4. Total Synthesis of (−)-Tetrahydropalmatine via Chiral Formamidine Carbanions: Unexpected Behavior with Certain Ortho-Substituted Electrophiles
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1. A Modular Approach for Diversity‐Oriented Synthesis of 1,3‐ trans ‐Disubstituted Tetrahydroisoquinolines: Seven‐Step Asymmetric Synthesis of Michellamines B and C;Angewandte Chemie International Edition;2022-06-17
2. A Modular Approach for Diversity‐Oriented Synthesis of 1,3‐ trans ‐Disubstituted Tetrahydroisoquinolines: Seven‐Step Asymmetric Synthesis of Michellamines B and C;Angewandte Chemie;2022-06-17
3. Iridium-Catalyzed Enantioselective and Diastereoselective Hydrogenation of 1,3-Disubstituted Isoquinolines;ACS Catalysis;2020-02-10
4. Oxazolidines as Intermediates in the Asymmetric Synthesis of 3-Substituted and 1,3-Disubstituted Tetrahydroisoquinolines;The Journal of Organic Chemistry;2016-07-26
5. Asymmetric photoinduced electrocyclic ring closure of chiral aromatic enehydrazides. Application to the asymmetric synthesis of 3-aryl dihydroisoquinolones and tetrahydroisoquinolines.;Proceedings of The 19th International Electronic Conference on Synthetic Organic Chemistry;2015-10-30
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