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Published in 2021 at "Chemistry of Heterocyclic Compounds"
DOI: 10.1007/s10593-021-02985-5
Abstract: The intramolecular oxidative coupling of electron-rich aromatic groups in 5-(het)aryl-1-(het)arylalkyl-1H-1,2,3-triazoles was studied in detail. Under treatment with phenyliodoso bis(trifluoroacetate) and boron trifluoride etherate these substrates afforded products of either ortho/ortho or ortho/ipso coupling depending on…
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Keywords:
electron rich;
ortho ortho;
ortho;
aromatic groups ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b02910
Abstract: Design of C-H activation directing groups that can serve as electrophiles for subsequent cross-coupling significantly improves the step economy of synthetic applications of directed C-H functionalization. Through using a well-defined bifunctional template, palladium-catalyzed ortho-C-H alkenylation…
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Keywords:
functionalization using;
using bifunctional;
sequential ortho;
ipso functionalization ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b03674
Abstract: This work describes a method for the difunctionalization of aryl iodides to generate polysubstituted arenes via Pd catalysis. The reaction hinges on the unique interplay between norbornene and the metal catalyst to impart a guided…
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Keywords:
aryl iodides;
ipso alkylborylation;
alkylborylation aryl;
aryl ... See more keywords
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2
Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b04202
Abstract: A complementary site selective ortho- vs ipso-amination of aryl halides using non-electrophilic amine sources for construction of indole scaffolds is reported. A palladium-catalyzed alkyne insertion/C-H activation/palladacycle amination via merger of three easily diversified components including…
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Keywords:
ipso amination;
amination;
aryl halides;
amination aryl ... See more keywords