Enantioselective synthesis of (−)-indolizidine 239AB [(3R,5S,8aR)-3-butyl-5-(3-hydroxypropyl)-octahydroindolizine]
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference11 articles.
1. Alkaloids from dendrobatid poison frogs: trans-decahydroquinolines and indolizidines
2. Alkaloids from Dendrobatid Frogs: Structures of Two ω-Hydroxy Congeners of 3-Butyl-5-Propylindolizidine and Occurrence of 2,5-Disubstituted Pyrrolidines and a 2,6-Disubstituted Piperidine
3. General entry to the 3,5-disubstituted indolizidine class of dendrobatid alkaloids. Total syntheses of both enantiomers of indolizidines 195B, 223AB, 239AB, and 239CD from a common chiral synthon
4. Total synthesis of (+) monomorine I from chiral cyclic β-enamino ester
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1. Reactivity of indolizines in organic synthesis;Synthetic Communications;2016-05-02
2. Synthesis of thieno[3,4-b]pyrrole derivatives based on the reaction of 1-methyl-2-nitromethylenepyrrolidine with isothiocyanates;Tetrahedron Letters;2014-10
3. Efficient synthesis of indolizines and new imidazo[1,2-a]pyridines via the expected cyclization of aromatic cycloimmonium ylides with electron deficient alkynes and ethyl cyanoformate;Tetrahedron Letters;2013-11
4. Enantioselective access to (−)-indolizidines 167B, 209D, 239AB, 195B and (−)-monomorine from a common chiral synthon;Tetrahedron;2012-01
5. Tandem ene-reaction/hydroamination of amino-olefin and -allene compounds catalyzed by Bi(OTf)3;Chemical Communications;2011
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