Synthesis and Catalytic Reactions -- 专题文献

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专题：Synthesis and Catalytic Reactions

最新文献

8-Quinox Cobalt Catalyst Enables the Reductive Alkylative Addition of Sulfinylamines with Unactivated Alkyl Halides

Microwave-enhanced additive-free C–H amination of benzoxazoles catalysed by supported copper

Synthesis of 6-ethoxyphenyl 4-fluorobenzenesulfonate-tagged thiosemicarbazones as carbonic anhydrase inhibitors: In-vitro and in silico approach

Late-Stage C–H Functionalization of Nimesulide via (Nimesulide)(3,5-dimethylisoxazol-4-yl)iodonium Salt Formation

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Oxone®-mediated Dakin-like reaction to synthesize hydroxyarenes: an approach using pyrazolo[1,5-a]pyrimidines

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近5年高被引文献

Late-stage C–H functionalization offers new opportunities in drug discovery

C–H activation

Toolbox for Distal C–H Bond Functionalizations in Organic Molecules

Transition-Metal-Catalyzed, Coordination-Assisted Functionalization of Nonactivated C(sp³)–H Bonds

Photocatalytic Late-Stage C–H Functionalization

Single-atom logic for heterocycle editing

Arene diversification through distal C(sp ² )−H functionalization

Put a ring on it: application of small aliphatic rings in medicinal chemistry

Skeletal editing through direct nitrogen deletion of secondary amines

Nitrogen-Centered Radicals in Functionalization of sp² Systems: Generation, Reactivity, and Applications in Synthesis

专题：Synthesis and Catalytic Reactions

最新文献

8-Quinox Cobalt Catalyst Enables the Reductive Alkylative Addition of Sulfinylamines with Unactivated Alkyl Halides

Microwave-enhanced additive-free C–H amination of benzoxazoles catalysed by supported copper

Synthesis of 6-ethoxyphenyl 4-fluorobenzenesulfonate-tagged thiosemicarbazones as carbonic anhydrase inhibitors: In-vitro and in silico approach

Late-Stage C–H Functionalization of Nimesulide via (Nimesulide)(3,5-dimethylisoxazol-4-yl)iodonium Salt Formation

Sustainable synthesis of 1-thiol-3-alkyl bicyclo[1.1.1]pentanes via electron donor–acceptor complex photoactivation: a metal- and additive-free strategy for bioisostere design

Exploring the SAR of 1,2,3‐Triazoles as Tumor‐Associated Carbonic Anhydrases IX and XII Inhibitors for Anticancer Applications

Structural Optimizations on the Scaffold of 7H‐Pyrrolo[2,3‐d]Pyrimidine to Develop Potent iNOS Inhibitors With Improved Antiarthritis Activity In Vivo

Comprehensive Insights Into Sulfanilamido‐Based Medicinal Design and Research

Oxone®-mediated Dakin-like reaction to synthesize hydroxyarenes: an approach using pyrazolo[1,5-a]pyrimidines

Research Advances in the Synthetic Methodologies of N-Trifluoromethylamides

近5年高被引文献

Late-stage C–H functionalization offers new opportunities in drug discovery

C–H activation

Toolbox for Distal C–H Bond Functionalizations in Organic Molecules

Transition-Metal-Catalyzed, Coordination-Assisted Functionalization of Nonactivated C(sp3)–H Bonds

Photocatalytic Late-Stage C–H Functionalization

Single-atom logic for heterocycle editing

Arene diversification through distal C(sp 2 )−H functionalization

Put a ring on it: application of small aliphatic rings in medicinal chemistry

Skeletal editing through direct nitrogen deletion of secondary amines

Nitrogen-Centered Radicals in Functionalization of sp2 Systems: Generation, Reactivity, and Applications in Synthesis

**Sustainable synthesis of 1-thiol-3-alkyl bicyclo[1.1.1]pentanes via electron donor–acceptor complex photoactivation: a metal- and additive-free strategy for bioisostere design**

Transition-Metal-Catalyzed, Coordination-Assisted Functionalization of Nonactivated C(sp³)–H Bonds

Arene diversification through distal C(sp ² )−H functionalization

Nitrogen-Centered Radicals in Functionalization of sp² Systems: Generation, Reactivity, and Applications in Synthesis