![Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0021951722000926-gr5.jpg)
Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect
![Bioisosteres of the Phenyl Ring: Recent Strategic Applications in Lead Optimization and Drug Design | Journal of Medicinal Chemistry Bioisosteres of the Phenyl Ring: Recent Strategic Applications in Lead Optimization and Drug Design | Journal of Medicinal Chemistry](https://pubs.acs.org/cms/10.1021/acs.jmedchem.1c01215/asset/images/medium/jm1c01215_0140.gif)
Bioisosteres of the Phenyl Ring: Recent Strategic Applications in Lead Optimization and Drug Design | Journal of Medicinal Chemistry
![A green and sustainable approach for the synthesis of 1,5-benzodiazepines and spirooxindoles in one-pot using a MIL-101(Cr) metal–organic framework as ... - New Journal of Chemistry (RSC Publishing) DOI:10.1039/D1NJ03176G A green and sustainable approach for the synthesis of 1,5-benzodiazepines and spirooxindoles in one-pot using a MIL-101(Cr) metal–organic framework as ... - New Journal of Chemistry (RSC Publishing) DOI:10.1039/D1NJ03176G](https://pubs.rsc.org/image/article/2021/NJ/d1nj03176g/d1nj03176g-f2_hi-res.gif)
A green and sustainable approach for the synthesis of 1,5-benzodiazepines and spirooxindoles in one-pot using a MIL-101(Cr) metal–organic framework as ... - New Journal of Chemistry (RSC Publishing) DOI:10.1039/D1NJ03176G
![Nickel(II)–NΛNΛO Pincer Type Complex-Catalyzed N-alkylation of Amines with Alcohols via the Hydrogen Autotransfer Reaction | The Journal of Organic Chemistry Nickel(II)–NΛNΛO Pincer Type Complex-Catalyzed N-alkylation of Amines with Alcohols via the Hydrogen Autotransfer Reaction | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.0c00530/asset/images/large/jo0c00530_0001.jpeg)
Nickel(II)–NΛNΛO Pincer Type Complex-Catalyzed N-alkylation of Amines with Alcohols via the Hydrogen Autotransfer Reaction | The Journal of Organic Chemistry
![Stepwise Mechanism for the Bromination of Arenes by a Hypervalent Iodine Reagent | The Journal of Organic Chemistry Stepwise Mechanism for the Bromination of Arenes by a Hypervalent Iodine Reagent | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.9b02784/asset/images/medium/jo9b02784_0005.gif)
Stepwise Mechanism for the Bromination of Arenes by a Hypervalent Iodine Reagent | The Journal of Organic Chemistry
![Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0021951722000926-gr6.jpg)
Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect
![Stepwise Mechanism for the Bromination of Arenes by a Hypervalent Iodine Reagent | The Journal of Organic Chemistry Stepwise Mechanism for the Bromination of Arenes by a Hypervalent Iodine Reagent | The Journal of Organic Chemistry](https://pubs.acs.org/cms/10.1021/acs.joc.9b02784/asset/images/large/jo9b02784_0001.jpeg)
Stepwise Mechanism for the Bromination of Arenes by a Hypervalent Iodine Reagent | The Journal of Organic Chemistry
![Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes | JACS Au Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes | JACS Au](https://pubs.acs.org/cms/10.1021/jacsau.1c00477/asset/images/large/au1c00477_0001.jpeg)
Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes | JACS Au
![Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0021951722000926-gr3.jpg)
Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect
![Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0021951722000926-gr7.jpg)
Nitrogen-doped carbon supported nanocobalt for the synthesis of functionalized triazines via oxidative cleavage of biomass derived vicinal diols as carbon synthons - ScienceDirect
![MOF-enabled confinement and related effects for chemical catalyst presentation and utilization - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D1CS00968K MOF-enabled confinement and related effects for chemical catalyst presentation and utilization - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D1CS00968K](https://pubs.rsc.org/image/article/2022/CS/d1cs00968k/d1cs00968k-f2_hi-res.gif)
MOF-enabled confinement and related effects for chemical catalyst presentation and utilization - Chemical Society Reviews (RSC Publishing) DOI:10.1039/D1CS00968K
![Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes | JACS Au Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes | JACS Au](https://pubs.acs.org/cms/10.1021/jacsau.1c00477/asset/images/large/au1c00477_0002.jpeg)
Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes | JACS Au
![Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes | JACS Au Molecularly Engineering Defective Basal Planes in Molybdenum Sulfide for the Direct Synthesis of Benzimidazoles by Reductive Coupling of Dinitroarenes with Aldehydes | JACS Au](https://pubs.acs.org/cms/10.1021/jacsau.1c00477/asset/images/large/au1c00477_0006.jpeg)