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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c00417
Abstract: It has always been a challenge in free radical chemistry to control site selectivity during the reaction of free radicals with aromatic rings. Herein, we report the site-selective carboxylation of anisoles through the direct reaction…
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Keywords:
selective carboxylation;
carboxylation;
ligand promoted;
para selective ... See more keywords
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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.6b03741
Abstract: A method for the para-selective alkylation of a variety of arenesulfonamides and aromatic sulfones with 1-alkenes by cooperative nickel/aluminum catalysis has been developed. Taking advantage of the sulfornyl functionality serving as a removable ortho-directing group,…
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Keywords:
nickel aluminum;
selective alkylation;
para selective;
aluminum catalysis ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b03451
Abstract: An efficient para-alkylation of primary and secondary anilines with a variety of sterically encumbered alkenes using a simple β-diketiminato scandium catalyst is reported. This protocol features 100% atom economy, excellent chemo- and regioselectivity, broad substrate…
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Keywords:
scandium catalyzed;
selective alkylation;
para selective;
alkylation aromatic ... See more keywords
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1
Published in 2022 at "ACS macro letters"
DOI: 10.1021/acsmacrolett.2c00541
Abstract: Postpolymerization modification of polystyrene (PS) can afford numerous value-added materials with different functions and applications, but it has been hampered by the lack of efficient methods. We report herein a highly efficient and para-selective conversion…
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Keywords:
providing versatile;
efficient para;
versatile platform;
highly efficient ... See more keywords
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0
Published in 2017 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.6b12907
Abstract: Pd-catalyzed highly para-selective arylations of monosubstituted simple arenes with arylboronic acids to widely existed biaryls have been developed. Inspired by requisite amide-directing groups in reported selective oxidative couplings, amide ligands, especially DMF, are designed and…
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Keywords:
monosubstituted simple;
highly para;
simple arenes;
para selective ... See more keywords
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Published in 2018 at "Nature Communications"
DOI: 10.1038/s41467-018-07069-1
Abstract: Selective creation of quaternary carbon centers has been a long-standing challenge in synthetic chemistry. We report here the chromium-catalyzed, para-selective formation of arylated quaternary carbon centers by alkylative reactions of benzamide derivatives with tertiary alkylmagnesium…
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Keywords:
chromium catalyzed;
carbon;
carbon centers;
para selective ... See more keywords
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Published in 2017 at "Chemical communications"
DOI: 10.1039/c7cc01476g
Abstract: Aryl homocoupling reactions via meta- and ortho-selective C-H activation have been achieved on surfaces, but the highly important para-selective C-H activation has not been reported yet. Combined with scanning tunneling microscopy, time-of-flight secondary ion mass…
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Keywords:
selective activation;
homocoupling tetrafluorobenzene;
para selective;
dehydrogenative homocoupling ... See more keywords
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Published in 2019 at "Chemical communications"
DOI: 10.1039/c8cc09129c
Abstract: A novel palladium catalyzed highly para-selective C-H difluoromethylation of electron-deficient aromatic carbonyls was developed. Diverse substituted aromatic ketones and benzoates were selectively difluoromethylated at the remote para-site of carbonyl groups in moderate to good yields.…
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Keywords:
para selective;
selective difluoromethylation;
aromatic carbonyls;
catalyzed para ... See more keywords
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Published in 2021 at "Chemical communications"
DOI: 10.1039/d1cc06210g
Abstract: para-Selective hydroxylation of alkyl aryl ethers is established, which proceeds with a ruthenium(II) catalyst, hypervalent iodine(III) and trifluoroacetic anhydride via a radical mechanism. This protocol tolerates a wide scope of substrates and provides a facile…
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Keywords:
aryl ethers;
hydroxylation alkyl;
para selective;
selective hydroxylation ... See more keywords
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2
Published in 2023 at "Organic Chemistry Frontiers"
DOI: 10.1039/d3qo00342f
Abstract: A Hexafluoroisopropanol-promoted highly regioselective Friedel-Crafts alkylation of arenes has been developed in this study. Various arenes, including anilides, anisoles, and phenols, were compatible with the reaction, leading to the para-alkylated...
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Keywords:
alkylation anilines;
para selective;
alkylation;
hfip promoted ... See more keywords