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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02937
Abstract: An efficient difunctionalization at C5/C8 of imidazo[1,2-a]pyrazines has been developed using disulfides and Grignard reagents under cheap cobalt catalysis. This one-pot, two-step, three-component transformation is performed under mild conditions; various Grignard reagents (aryl and alkyl)…
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Keywords:
grignard reagents;
imidazo pyrazines;
catalyzed dual;
dual bond ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c03666
Abstract: An efficient and straightforward approach for the synthesis of trifluoromethyl-decorated benzo[de][1,8]naphthyridines has been achieved via the Rh(III)-catalyzed dual C-H activation and cascade annulation of benzimidates and CF3-imidoyl sulfoxonium ylides. The novel transformation involves the formation…
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Keywords:
synthesis trifluoromethyl;
decorated benzo;
catalyzed dual;
benzo naphthyridines ... See more keywords
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Published in 2018 at "ACS Catalysis"
DOI: 10.1021/acscatal.8b01011
Abstract: A highly atom-economical, chemoselective, and stereoselective Lewis base (LB)-catalyzed dual umpolung domino Michael reaction between cyclohexadienones and alkynyl esters has been developed. PPh3, as a LB catalyst, afforded either the hydroindole-2-carboxylates or hydrobenzofuran-2-carboxylates 3 as…
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Keywords:
umpolung domino;
hydrobenzofuran carboxylates;
domino michael;
catalyzed dual ... See more keywords
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Published in 2020 at "Chemical communications"
DOI: 10.1039/d0cc01172j
Abstract: In this work, CuSO4 is utilized as a practical redox catalyst for tandem dual annulation in the synthesis of indole-fused tetracyclic heteroacenes, which are important skeletons in both medicinal chemistry and materials chemistry. The preparation…
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Keywords:
cuso4 catalyzed;
chemistry;
tetracyclic heteroacenes;
dual annulation ... See more keywords