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Carcinogens / Origin of life / Pyridine / Chemistry / Aromatic hydrocarbon / Astrochemistry


Amine α-heteroarylation via photoredox catalysis: a homolytic aromatic substitution pathway
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Document Date: 2014-10-24 14:14:27


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File Size: 1,22 MB

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City

Weinheim / Wiley-Interscience / /

Company

E. D. Funder D. D. / Merck / Amgen / Boc group / Bristol-Myers Squibb / /

Country

Jordan / United States / /

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Facility

Princeton University / Plant Pathol / /

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IndustryTerm

exocyclic benzylic site / photoredox protocol / Online Published / anionic leaving / Online EDGE ARTICLE Cite / caffeine ring systems / desired a-amino arylation products / pharmaceutical research / chloro-leaving groups / heterocyclic ring systems / arylation coupling site / biological systems / Online Edge Article Published / a-amino coupling protocol / arylation protocol / a-heteroaryl amine product / non-electrophilic site / /

Organization

Princeton University / Royal Society of Chemistry / /

Person

P. O'Brien / R. A. Pascal / Jr / D. Zewge / K. R. Campos / J. I. Goldsmith / A. Klapars / J. D. Slinker / R. Rohl / C. Chen / J. J. Bouska / V / S. Bernhard / Nat / J. L. McGrath / G. Zhou / G. Barker / Christopher K. Prier / G. G. Malliaras / P. G. Dormer / D. Stead / S. H. Rosenberg / V / Y. Luo / L. R. Kleinberg / V / Yuan Hu / Amine / J. H. Waldman / /

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Position

proposed model for the observed regioselectivity / representative / T. D. / /

Product

acetic acid / /

ProvinceOrState

New Jersey / New York / /

Technology

a-amino coupling protocol / photoredox protocol / arylation protocol / PDF / /

URL

www.rsc.org/chemicalscience / /

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