Enantioselective syntheses of two 5, 9E diastereomers of 223V, an alkaloid from the poison frog Dendrobates pumilio
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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2. Ammonia chemical ionization tandem mass spectrometry in structure determination of alkaloids. I. Pyrrolidines, piperidines, decahydroquinolines, pyrrolizidines, indolizidines, quinolizidines and an azabicyclo[5.3.0]decane
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4. New classes of amidine, indolizidine and quinolizidine alkaloids from a poison-frog, (dendrobatidae)
5. Alkaloids from a Panamanian Poison Frog, Dendrobates speciosus: Identification of Pumiliotoxin-A and Allo-pumiliotoxin Class Alkaloids, 3,5-Disubstituted Indolizidines, 5-Substituted 8-Methylindolizidines, and a 2-Methyl-6-nonyl-4-hydroxypiperidine
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1. Divergent Synthesis of Decahydroquinoline‐Type Poison‐Frog Alkaloids;ChemistrySelect;2022-02-03
2. Total Synthesis of Decahydroquinoline Poison Frog Alkaloids ent-cis-195A and cis-211A;Molecules;2021-12-12
3. Divergent Syntheses of Pumiliotoxin‐Type Poison‐Frog Alkaloids;ChemistrySelect;2021-02-24
4. Palladium-catalyzed asymmetric allylic C-H alkylation of 1,4-dienes and glycine Schiff bases;Science China Chemistry;2020-03-13
5. Synthesis of 8-deoxypumiliotoxin 193H and 9-deoxyhomopumiliotoxin 207O;Tetrahedron Letters;2018-10
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