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Amino acid / Nitrogen metabolism / Zwitterions / Decarboxylation / Carboxylic acid / Aryl radical / Nitrile / Dakin–West reaction / Chemistry / Organic chemistry / Substitution reactions


Communication pubs.acs.org/JACS Decarboxylative Arylation of α‑Amino Acids via Photoredox Catalysis: A One-Step Conversion of Biomass to Drug Pharmacophore
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Document Date: 2014-04-30 10:02:02


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File Size: 1,09 MB

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City

Ru / New York / /

Company

Merck / Cambridge University Press / Cox / Amgen / W. H. Freeman and Co. / Boc / Lawrence S. A. / MacMillan / ASSOCIATED CONTENT / /

Country

United States / /

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Event

FDA Phase / /

Facility

Princeton University / Shanghai Institute of Organic Chemistry / /

IndustryTerm

decarboxylative functionalization protocol / decarboxylative technologies / chemical transformations / pharmaceuticals / α-amino acid protecting / desired α-amino arylation product / different carbamate systems / zero−zero spectroscopic energy / decarboxylative arylation protocol / highvalue chemical products / /

Organization

American Chemical Society / Cambridge University / Princeton University / Drug Pharmacophore Zhiwei Zuo and David W. C. MacMillan* Merck Center for Catalysis / Shanghai Institute of Organic Chemistry / /

Person

Yong Yan / /

Position

D. J. / Communication AUTHOR INFORMATION Corresponding Author dmacmill@princeton.edu Notes The authors / /

Product

PF6 / Amino Acid / Csp3 / /

ProvinceOrState

New Jersey / Ir / /

PublishedMedium

Journal of the American Chemical Society / /

Technology

decarboxylative arylation protocol / biomass conversion / coupling protocol / decarboxylative functionalization protocol / dielectric / /

URL

http /

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