A new entry into the synthesis of the strychnos indole alkaloids containing 19,20-double bond via the thio-claiser rearrangement
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Total synthesis of (±)-fluorocurarine, the racemate of a Calabash-curare alkaloid
2. A new entry into the synthesis of the nine-membered indole alkaloids related to cleavamine. A stereospecific synthesis of (dl)-4.alpha.-dihydrocleavamine and (dl)-quebrachamine via the thio-Claisen rearrangement
3. New synthetic route to mono- and di-γδ-unsaturated NN-dialkylthionamides by the thio-Claisen rearrangement based on acyclic NN-dalkylthioamides
4. Studies on Thioamides. II. Application of Thioamides in Bischler-Napieralski Reaction.
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1. Chemical Reactions of Indole Alkaloids That Enable Rapid Access to New Scaffolds for Discovery;SynOpen;2023-03-07
2. Synthesis of 2-Azabicyclo[m.n .0]-Alkanes and Their Application towards the Synthesis of Strychnos and Stemona Classes of Alkaloids;European Journal of Organic Chemistry;2020-05-27
3. Total Synthesis of Aspidosperma and Strychnos Alkaloids through Indole Dearomatization;Chemistry – A European Journal;2019-05-16
4. Formation of Nitriles, Carboxylic Acids, and Derivatives by Alkylation, Acylation, and Substitution;Comprehensive Organic Transformations;2018-02-28
5. Exploratory studies toward a total synthesis of pericine (subincanadine E);Tetrahedron;2015-04
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