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Nam T. S. Phan
Researcher at Vietnam National University, Ho Chi Minh City
Publications - 143
Citations - 5793
Nam T. S. Phan is an academic researcher from Vietnam National University, Ho Chi Minh City. The author has contributed to research in topics: Catalysis & Heterogeneous catalysis. The author has an hindex of 32, co-authored 130 publications receiving 5049 citations. Previous affiliations of Nam T. S. Phan include Georgia Institute of Technology & University of Sheffield.
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On the Nature of the Active Species in Palladium Catalyzed Mizoroki–Heck and Suzuki–Miyaura Couplings – Homogeneous or Heterogeneous Catalysis, A Critical Review
TL;DR: A wide array of forms of palladium has been utilized as precatalysts for Heck and Suzuki coupling reactions over the last 15 years as mentioned in this paper, and there are now many suggestions in the literature that narrow the scope of types of precatalyst that may be considered true catalysts in these coupling reactions.
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Expanding Applications of Metal−Organic Frameworks: Zeolite Imidazolate Framework ZIF-8 as an Efficient Heterogeneous Catalyst for the Knoevenagel Reaction
TL;DR: In this article, a highly porous zeolite imidazolate framework (ZIF-8) was synthesized by a solvothermal method, and used as an efficient heterogeneous catalyst for the Knoevenagel reaction.
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Highly accessible catalytic sites on recyclable organosilane-functionalized magnetic nanoparticles: An alternative to functionalized porous silica catalysts
TL;DR: In this paper, diaminosilane-functionalized cobalt spinel ferrite (CoFe2O4) magnetic nanoparticles are synthesized and used as efficient heterogeneous base catalysts for the Knoevenagel condensation of aromatic and hetero-aromatic aldehydes with malononitrile.
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Expanding the utility of one-pot multistep reaction networks through compartmentation and recovery of the catalyst.
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Metal–organic frameworks for catalysis: the Knoevenagel reaction using zeolite imidazolate framework ZIF-9 as an efficient heterogeneous catalyst
TL;DR: The ZIF-9 catalyst was easily isolated from the reaction mixture by simple filtration and reused several times without a significant degradation in activity and there was no contribution from leached active species and conversion was only being possible in the presence of the solid catalyst as discussed by the authors.