Chemoselective reductions of nitroaromatics in water at room temperature
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Transitioning organic synthesis from organic solvents to water. What's your E Factor?Safe and Selective Nitro Group Reductions Catalyzed by Sustainable and Recyclable Fe/ppm Pd Nanoparticles in Water at Room Temperature.Design, synthesis and biological activity of pyrazinamide derivatives for anti-Mycobacterium tuberculosis.An azobenzene-containing metal-organic framework as an efficient heterogeneous catalyst for direct amidation of benzoic acids: synthesis of bioactive compounds.Reactivity of Polar Organometallic Compounds in Unconventional Reaction Media: Challenges and OpportunitiesMagnetically Recyclable Metal-Organic Framework@Fe3 O4 Composite-Catalyzed Facile Reduction of Nitroarene Compounds in Aqueous MediumEvaluation of Nitrobenzyl Derivatives of Camptothecin as Anti-Cancer Agents and Potential Hypoxia Targeting Prodrugs
P2860
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P2860
Chemoselective reductions of nitroaromatics in water at room temperature
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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name
Chemoselective reductions of nitroaromatics in water at room temperature
@en
Chemoselective reductions of nitroaromatics in water at room temperature.
@nl
type
label
Chemoselective reductions of nitroaromatics in water at room temperature
@en
Chemoselective reductions of nitroaromatics in water at room temperature.
@nl
prefLabel
Chemoselective reductions of nitroaromatics in water at room temperature
@en
Chemoselective reductions of nitroaromatics in water at room temperature.
@nl
P2860
P356
P1433
P1476
Chemoselective reductions of nitroaromatics in water at room temperature
@en
P2093
Bruce H Lipshutz
Sean M Kelly
P2860
P304
P356
10.1021/OL403079X
P407
P577
2013-12-16T00:00:00Z