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Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c00308
Abstract: Fe(II)-phosphine complex [Fe(dpbz)]Cl2 was demonstrated to be effective for the intramolecular C(sp3)-H amination of organic azides. This catalyst exhibited a high catalytic capacity for the transformations from α-azido amides to imidazolinones. Cyclization of simple aliphatic…
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Keywords:
intramolecular sp3;
phosphine complex;
sp3 amination;
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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b00533
Abstract: A novel, simple, and practical visible-light-mediated intramolecular α-C(sp3)-H imination of tertiary aliphatic amines containing β-O-aryl oximes leading to N-heterocycles has been developed. The reaction was performed well at rt with tolerance of some functional groups.…
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Keywords:
sp3 imination;
sole requirement;
visible light;
light sole ... See more keywords
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Published in 2019 at "Chemical communications"
DOI: 10.1039/c8cc09100e
Abstract: Herein, a highly exothermic primary amine-polyvalent iodine reaction has been used successfully for selective functionalization of acidic C(sp3)-H groups for a dehydrogenative C-H imination reaction by 4H elimination. Overall, C(sp3)-H imination at 1,5 distances was…
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Keywords:
sp3 imination;
imination;
imination using;
using phi ... See more keywords
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Published in 2021 at "Chemical communications"
DOI: 10.1039/d1cc04573c
Abstract: Herein, we describe a soluble iron(II)-phthalocyanine, [FeII(tBu4Pc)(py)2] (Pc = phthalocyaninato(2-)), as an effective catalyst in intramolecular C(sp3)-H bond amination, with alkyl azides as the nitrogen source, to afford the amination products in moderate to excellent…
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Keywords:
iron phthalocyanine;
amination alkyl;
soluble iron;
alkyl azides ... See more keywords