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Published in 2017 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2017.09.045
Abstract: Abstract This paper describes our efforts toward the asymmetric synthesis of sarain A which led to efficient preparation of a functionalized azabicyclo[3.3.1]nonane moiety. The key to the synthesis relied on a base-catalyzed asymmetric Diels-Alder cycloaddition…
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Keywords:
nonane moiety;
asymmetric synthetic;
azabicyclo nonane;
sarain ... See more keywords
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1
Published in 2020 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2020.152006
Abstract: Abstract Brefeldin A (BFA) is a fungal metabolite that displays a wide range of biological activities making it an attractive target for drug discovery. To explore the biological potential of the BFA scaffold an amine-macrocycle…
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Keywords:
bfa;
azabicyclo nonane;
scaffolds brefeldin;
synthesis ... See more keywords
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Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c00912
Abstract: Novel asymmetric synthetic routes to (+)-uleine and (-)-tubifolidine are reported herein. The regioselective formation of enol triflates from 2-azabicyclo[3.3.1]nonane ketones followed by indolizations of the resultant ene-hydrazides allowed the efficient construction of key indole intermediates,…
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Keywords:
routes uleine;
tubifolidine general;
azabicyclo nonane;
synthetic routes ... See more keywords
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Published in 2022 at "Current organic synthesis"
DOI: 10.2174/1570179419666220413092052
Abstract: BACKGROUND Literature survey suggested various methods of synthesis of the 3-azabicyclo[3.3.1] nonanes which includes, Mannich reaction, α, α'-Annelation of Cyclic Ketones or through Enamines, Michael addition, Intramolecular Cyclizations etc. However, a mechanism following a Michael…
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Keywords:
nonane one;
reaction;
azabicyclo nonane;
synthesis spiro ... See more keywords