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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c01654
Abstract: The cyclization-coupling reaction of 2-bromoaryl ketones and terminal alkynes is first realized by copper catalysis, which produces polyfunctional naphthyl aryl ethers in moderate to excellent yields with broad substrate scope and good functional group tolerance.…
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Keywords:
cyclization coupling;
bromoaryl ketones;
ketones terminal;
endo dig ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02531
Abstract: We report a Cu(II)-catalyzed cyclization/coupling of alkenyl aldimines with arylzinc reagents to create indole-3-diarylmethane derivatives (Sapkota et al. ChemRxiv 2022, DOI: 10.26434/chemrxiv-2022-d6qn). The current reaction provides a unified modular route from readily available starting materials…
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Keywords:
catalyzed cyclization;
aldimines arylzinc;
cyclization coupling;
alkenyl aldimines ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b01846
Abstract: A cobalt-N-heterocyclic carbene catalyst promotes a tandem radical cyclization/C-C coupling reaction between tosylamide-tethered bromo-alkenes and aryl N-H imines initiated by chelation-assisted arene C-H activation, affording 3-(arylmethyl)pyrrolidine derivatives in moderate to good yields. The reaction tolerates…
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Keywords:
tandem radical;
radical cyclization;
cobalt catalyzed;
activation ... See more keywords