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Published in 2019 at "Tetrahedron"
DOI: 10.1016/j.tet.2019.04.028
Abstract: The application of thioallenoates to catalytic enantioselective [2+2]-cycloadditions with unactivated alkenes is reported.In many cases, the thioallenoates examined exhibit superior reactivity and selectivity compared to the alkoxy analogs generally used in these cycloadditions.
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Keywords:
thioallenoates catalytic;
enantioselective cycloadditions;
cycloadditions unactivated;
catalytic enantioselective ... See more keywords
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Published in 2020 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2019.151540
Abstract: Abstract A simple and efficient copper-catalyzed aminooxygenation of unactivated alkenes with commercially available (2,2,6,6-tetramethylpiperidin-1-yl)-oxyl (TEMPO) as an oxygen source is reported. With this protocol, a variety of functionalized pyrrolidones were obtained in good to excellent…
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Keywords:
catalyzed aminooxygenation;
unactivated alkenes;
aminooxygenation unactivated;
copper catalyzed ... See more keywords
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Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c01395
Abstract: The base-induced reaction of aryl diazonium salts with commercially available CF3SO2Na/CF2HSO2Na allows for the generation of the corresponding diazene radicals along with fluoromethyl radicals. The addition of fluoromethyl radicals to alkenes with subsequent diazene trapping…
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Keywords:
promoted radical;
azofluoromethylation unactivated;
azofluoromethylation;
unactivated alkenes ... See more keywords
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.0c04225
Abstract: A novel visible-light-induced radical tandem trifluoromethylation/cyclization of unactivated alkenes with sodium perfluoroalkanesulfinates (Rf = CF3, C3F7, C4F9, C6F13, C8F17) under air atmosphere has been developed. A range of quinazolinones containing unactivated alkene moiety and sodium…
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Keywords:
unactivated alkenes;
cyclization unactivated;
self catalyzed;
perfluoroalkyl substituted ... See more keywords
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c03991
Abstract: Chemo- and regioselectively nickel-catalyzed reductive benzylarylation of unactivated alkenes with o-bromobenzyl chlorides is disclosed herein, in which electrophiles participate through a single-component double-site approach. Moreover, its utility is underscored by the concise synthesis of bioactive…
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Keywords:
nickel catalyzed;
chemo;
benzylarylation unactivated;
unactivated alkenes ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c03247
Abstract: A general and mild strategy involving three-component carboarylation of unactivated alkenes with protic C(sp3)-H feedstocks via photoredox catalysis was reported. This catalytic system is compatible with a broad range of unactivated alkenes, cyano-substituted arenes, and…
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Keywords:
component carboarylation;
sp3 feedstocks;
protic sp3;
three component ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.2c04337
Abstract: Herein, we report visible-light-driven hydroacylation of unactivated alkenes. We employed benzimidazolines as new acyl donors and achieved perfect regioselectivity, high functional-group tolerance, and excellent substrate generality. We also performed mechanistic experiments to elucidate the detailed…
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Keywords:
hydroacylation unactivated;
light driven;
visible light;
acyl donors ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.2c04356
Abstract: A redox-neutral mild methodology for the allylic C-H alkylation of unactivated alkenes with diazo compounds is demonstrated. The developed protocol is able to bypass the possibility of the cyclopropanation of an alkene upon its reaction…
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Keywords:
functionalization unactivated;
alkenes diazocarbonyl;
catalyzed allylic;
rhodium catalyzed ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c00085
Abstract: An expeditious and novel nickel-catalyzed selective arylhydroxylation of unactivated alkenes with arylboronic acids was developed. This protocol is compatible with β,γ- and γ,δ-alkene amides, including traditionally challenging internal alkenes, to provide important β-arylethylalcohol scaffolds. The…
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Keywords:
arylhydroxylation unactivated;
selective arylhydroxylation;
nickel catalyzed;
unactivated alkenes ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c00651
Abstract: An expeditious copper-catalyzed three-component hydroxyperfluoroalkylation of unactivated alkenes starting from commercially available perfluoroalkyl iodides and an O2 molecule from air as the oxygen source was developed. The Cu/B2pin2 catalytic system offered a novel pattern for…
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Keywords:
perfluoroalkyl;
perfluoroalkyl alcohols;
copper catalyzed;
hydroxyperfluoroalkylation unactivated ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c00771
Abstract: A novel Pd-catalyzed enantioselective aminochlorination of alkenes via a 6-endo cyclization is reported herein, which provides easy access to a wide array of structurally diverse 3-chloropiperidines in good yields with excellent enantioselectivities. Notably, both an…
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Keywords:
aminochlorination unactivated;
palladium catalyzed;
asymmetric palladium;
aminochlorination ... See more keywords