Asymmetric steering of the Pictet-Spengler reaction by means of amino acid esters as chiral auxiliary groups
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
1. Asymmetric Synthesis of Isoquinoline Alkaloids: (R)- and (S)-2-Ethoxycarbonyl-1-Formyl-6, 7-Dimethoxy-1,2,3,4-Tetrahydroisoquinoline as Versatile Precursors
2. Stereospecific pictet-spengler reaction: synthesis of cis (+)-(1S, 12bR)-1-aminoindoloquinolizidine from a pure α-(S)-aminoaldehyde derivative
3. Diastereo- and enantio-selectivity in the Pictet–Spengler reaction
4. Stereospecificity in the Pictet-Spengler reaction kinetic vs thermodynamic control
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1. Bioactive Quinolactacins and Structurally Related Pyrroloquinolones;Studies in Natural Products Chemistry;2019
2. Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds;Molecules;2018-04-18
3. The Pictet-Spengler Reaction Still on Stage;Current Pharmaceutical Design;2016-03-29
4. Selective synthesis of 4,5-dihydroimidazo- and imidazo[1,5-a]quinoxalines via modified Pictet–Spengler reaction;Tetrahedron Letters;2013-11
5. Pictet-Spengler Reaction Revisited: Engineering of Tetherd Biheterocycles into Annulated Polyheterocycles;Current Organic Synthesis;2012-05-01
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