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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c02931
Abstract: Hantzsch esters (HEs) served as two-carbon partners in a copper(I)-catalyzed enantioselective [3 + 2] annulation with racemic 2-(hetero)aryl-N-sulfonyl aziridines via kinetic resolution to provide pyrrolo[2,3-b]tetrahydropyridines containing multiple contiguous stereogenic centers including all-carbon quaternary centers in…
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Keywords:
annulation hantzsch;
asymmetric annulation;
hantzsch esters;
hantzsch ... See more keywords
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Published in 2025 at "Organic letters"
DOI: 10.1021/acs.orglett.4c04625
Abstract: Herein, we introduce a scandium-catalyzed synthetic strategy that provides access to a diverse and functionalized array of cyclobutene frameworks adorned with a quaternary carbon center. This approach broadens the synthetic repertoire of 2-alkynylnaphthols with alkenes,…
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Keywords:
annulation alkynylnaphthols;
cyclobutene frameworks;
access;
asymmetric annulation ... See more keywords
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Published in 2025 at "Organic letters"
DOI: 10.1021/acs.orglett.5c00064
Abstract: Highly asymmetric (3+3) annulation of diaziridines with oxiranes via C-N bond cleavage in diaziridine was achieved under 10 mol % of chiral copper(II) complex as the catalyst under mild reaction conditions. With Cu(OTf)2 as the…
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Keywords:
diaziridines oxiranes;
asymmetric annulation;
copper catalyzed;
catalyzed asymmetric ... See more keywords
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Published in 2018 at "Organic letters"
DOI: 10.1021/acs.orglett.8b02214
Abstract: The copper-catalyzed asymmetric [3 + 3] annulation of ethynyl benzoxazinanones with pyrazolones has been achieved, providing simple access to 1,4-dihydropyrano[2,3- c]pyrazole derivatives in moderate to excellent yields with excellent enantioselectivities (up to 99% ee). Compared…
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Keywords:
dihydropyrano;
annulation;
copper allenylidenes;
annulation copper ... See more keywords