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Published in 2017 at "Journal of Heterocyclic Chemistry"
DOI: 10.1002/jhet.2708
Abstract: p-Toluenesulfonic acid mediated formal [3+3] cyclization of 3-indolylmethanols with 3-isothiocyanato oxindoles was realized. This transformation allowed for the synthesis of a series of novel tetrahydro-β-carboline-1-thione spirooxindoles in moderate to excellent yields (up to 99%) with…
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Keywords:
acid mediated;
mediated formal;
indolylmethanols isothiocyanato;
cyclization indolylmethanols ... See more keywords
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Published in 2019 at "Tetrahedron"
DOI: 10.1016/j.tet.2018.11.016
Abstract: Abstract Quinones, precursors of aromatic structures, were firstly employed as the electrophiles for the organocatalytic Michael addition/cyclization cascade reaction with versatile 3-isothiocyanato oxindoles. Chiral bifunctional organocatalyst was appropriate for this enantioselective transformation to afford a…
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Keywords:
double arylation;
arylation isothiocyanato;
oxindoles stereocontrolled;
isothiocyanato oxindoles ... See more keywords
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Published in 2023 at "Chemical communications"
DOI: 10.1039/d3cc00376k
Abstract: Herein, previously unreported Fischer's base reactants serving as useful 2C building blocks in (3+2) cycloaddition reactions to build a library of bispiro[Fischer's base-oxindole] hybrids are described. These structurally intriguing products containing three adjacent quaternary stereocentres…
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Keywords:
fischer base;
acceptor donor;
base triggered;
isothiocyanato oxindoles ... See more keywords