Asymmetric pictet-spengler synthesis of tetrahydroisoquinolines. An enantioselective synthesis of (−)-laudanosine.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Isoquinolines,1981
2. Enantioselective synthesis of isoquinoline alkaloids
3. New Synthesis of 1-Benzyl-6, 7-dihydroxy-1, 2, 3, 4-tetrahydroisoquinoline Derivatives
4. A novel synthesis of 1,2,3,4-tetrahydroisoquinolines and a note on the reactivity of a 4-methoxy-derivative
5. Synthesis of E- and Z-vinyl ethers by the Horner–Wittig reaction
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1. A Catalytic Asymmetric Pictet–Spengler Platform as a Biomimetic Diversification Strategy toward Naturally Occurring Alkaloids;Journal of the American Chemical Society;2022-08-17
2. A modular approach to the bisbenzylisoquinoline alkaloids tetrandrine and isotetrandrine;Organic & Biomolecular Chemistry;2020
3. Cation−π Interactions in Organic Synthesis;Chemical Reviews;2018-12-03
4. Consecutive Ring Expansion and Contraction for the Synthesis of 1-Aryl Tetrahydroisoquinolines and Tetrahydrobenzazepines from Readily Available Heterocyclic Precursors;Angewandte Chemie International Edition;2018-04-17
5. Consecutive Ring Expansion and Contraction for the Synthesis of 1-Aryl Tetrahydroisoquinolines and Tetrahydrobenzazepines from Readily Available Heterocyclic Precursors;Angewandte Chemie;2018-04-17
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