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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.6b03772
Abstract: A cascade double C-H annulation of aldoximes with alkynes to produce benz[a]acridizinium salts is developed by using a simple catalytic system of [Cp*Rh(OAc)2]2 in the presence of Zn(OTf)2 with oxygen as the sole oxidant. In…
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Keywords:
aldoximes alkynes;
sole oxidant;
annulation aldoximes;
pot access ... See more keywords
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0
Published in 2018 at "Organic letters"
DOI: 10.1021/acs.orglett.8b01586
Abstract: A Mn(III)-catalyzed three-component cascade C-H/N-H functionalization of 2-aminopyridines with 2 equiv of dialkyl butyndioates leads to peri-condensed tricylic azines through a selective, but partly destructive, stoichiometry. A wide range of 2,11-diazatricyclo[5.3.1.04,11]undeca-1(10),4,6,8-tetraen-3-ones were thus obtained with…
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Keywords:
access peri;
peri condensed;
cascade;
pot access ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.8b04072
Abstract: Disclosed herein is a highly efficient strategy to fuse an aromatic ring to azoarenes for one-pot access to 5,6-phenanthrolinium skeletons via tandem ortho-C-H arylation and aryl quaternization. This protocol enables ortho-hindered azobenzenes to solely form…
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Keywords:
ring azoarenes;
azoarenes one;
aromatic ring;
pot access ... See more keywords
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2
Published in 2023 at "Organic Chemistry Frontiers"
DOI: 10.1039/d3qo00598d
Abstract: Herein, we report a novel one-pot method for synthesizing polysubstituted pyrrole derivatives via three-component reactions of alkenyl bromides, amines, and isocyanides. The conversion process is catalyzed by a Pd catalyst...
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Keywords:
catalyzed imine;
imine directed;
one pot;
directed one ... See more keywords