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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c00070
Abstract: Cyclobutanols undergo an oxidative ring expansion with Co(acac)2 and triplet oxygen to give 1,2-dioxanols. The formation of an alkoxy radical drives the regioselective cleavage of the ring on the more substituted side before insertion of…
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Keywords:
oxidative ring;
ring expansion;
cyclobutanols access;
expansion cyclobutanols ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c00125
Abstract: N-Functionalized C-fluoroalkyl amidines are attracting great attention due to their potential in pharmaceuticals. Herein, we report a Pd-catalyzed tandem reaction of azide with isonitrile and fluoroalkylsilane via a carbodiimide intermediate, providing facile access to N-functionalized…
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Keywords:
reaction azide;
functionalized fluoroalkyl;
access functionalized;
azide isonitrile ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b00884
Abstract: The synthesis and utilization of a class of 2,1-borazaronaphthyltrifluoroborate reagents that provide a general solution to the challenge of N-functionalization of the 2,1-borazaronaphthalene core is described. By adorning the nitrogen of this core with a…
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Keywords:
functionalized borazaronaphthalenes;
enables access;
photoredox catalysis;
access functionalized ... See more keywords
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Published in 2021 at "Chemical communications"
DOI: 10.1039/d0cc07307e
Abstract: Photoredox-mediated C-H bond alkylation of 6-aryl-2,2'-bipyridines with N-(acyloxy)phthalimides is reported. The reaction exhibits excellent functional group tolerance, including chiral aliphatic groups. The influence of the incorporated C6'-alkyl group on the photophysical properties of the corresponding…
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Keywords:
aryl bipyridines;
alkylation aryl;
functionalized luminescent;
access functionalized ... See more keywords