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Neil K. Garg
Researcher at University of California, Los Angeles
Publications - 221
Citations - 11291
Neil K. Garg is an academic researcher from University of California, Los Angeles. The author has contributed to research in topics: Catalysis & Total synthesis. The author has an hindex of 53, co-authored 203 publications receiving 9610 citations. Previous affiliations of Neil K. Garg include University of California, Berkeley & University of California.
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Journal ArticleDOI
Nickel-Catalyzed Cross-Couplings Involving Carbon-Oxygen Bonds
Brad M. Rosen,Kyle W. Quasdorf,Daniella A. Wilson,Na Zhang,Ana-Maria Resmerita,Neil K. Garg,Virgil Percec +6 more
TL;DR: Nickel-Catalyzed Cross-Couplings Involving Carbon-Oxygen Bonds Brad M. Rosen, Kyle W. Quasdorf, Daniella A. Wilson, Na Zhang, Ana-Maria Resmerita, Neil K. Garg, and Virgil Percec report on cross-coupling strategies for high-performance liquid chromatography of carbon dioxide and nitrogen.
Journal ArticleDOI
Conversion of amides to esters by the nickel-catalysed activation of amide C-N bonds
Liana Hie,Noah F. Fine Nathel,Tejas K. Shah,Emma L. Baker,Xin Hong,Yun-Fang Yang,Peng Liu,Kendall N. Houk,Neil K. Garg +8 more
TL;DR: It is demonstrated that amide carbon–nitrogen bonds can be activated and cleaved using nickel catalysts and is expected to lead to the further use of amides in the construction of carbon–heteroatom or carbon–carbon bonds using non-precious-metal catalysis.
Journal ArticleDOI
Breaking Amides using Nickel Catalysis
Jacob E. Dander,Neil K. Garg +1 more
TL;DR: Ni catalysis provides exciting new tools to build C-heteroatom and C-C bonds using an unconventional reactant (i.e., the amide), which is ideally suited for use in multi-step synthesis.
Journal ArticleDOI
Cross-coupling reactions of aryl pivalates with boronic acids.
TL;DR: The first cross-coupling of acylated phenol derivatives has been achieved in the presence of an air-stable Ni(II) complex, and the potential to utilize an aryl pivalate as a directing group has been demonstrated.
Journal ArticleDOI
Nickel-catalysed Suzuki–Miyaura coupling of amides
TL;DR: These studies demonstrate that amides, despite classically considered inert substrates, can be harnessed as synthons for use in reactions that form C-C bonds through cleavage of the C-N bond using non-precious metal catalysis.