Asymmetric synthesis of 3,5-disubstituted indolizidines by intermolecular addition of an allylsilane on an N-acyliminium ion
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference27 articles.
1. Alkaloids from dendrobatid poison frogs: trans-decahydroquinolines and indolizidines
2. 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
3. Asymmetric synthesis III. Enantiospecific synthesis of the natural 3r, 5r, 9r (−) gephyrotoxin-223 AB
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1. Recent Progress Towards Synthesis of the Indolizidine Alkaloid 195B;Current Organic Synthesis;2020-05-08
2. 4.4.40.72 Allylsilanes (Update 2020);SOS Knowledge Updates 2020/1;2020
3. C-H Functionalization of Amino Alcohols by Osmium Tetroxide/NMO or TPAP/NMO: Protecting Group-Free Synthesis of Indolizidines (-)-223AB and 3-epi -(-)-223AB;European Journal of Organic Chemistry;2019-12-19
4. An asymmetric synthesis of (+)-monomorine I;Tetrahedron: Asymmetry;2017-11
5. A short and modular approach towards 3,5-disubstituted indolizidine alkaloids;Organic & Biomolecular Chemistry;2016
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