# Synthesis and Catalytic Reactions

**Type:** Topics  
**Canonical URL:** https://scholariq.org/topics/synthesis-and-catalytic-reactions/

## Facts

| Field | Value |
| --- | --- |
| Description | This cluster of papers focuses on the catalytic C-H amination reactions, including nitrene transfer methods, enantioselective synthesis of aziridines, and the use of sulfoximines in medicinal chemistry. The research covers various metal-catalyzed approaches and their applications in the synthesis of biologically relevant compounds. |
| Domain | Physical Sciences |
| Field | Chemistry |
| OpenAlex ID | t12251 |
| Works | 30 |

## Topic papers all

Showing 15 of 30.

- [Review Article](https://scholariq.org/papers/review-article-2/)
- [Transition metal-catalyzed ketone-directed or mediated C–H functionalization](https://scholariq.org/papers/transition-metal-catalyzed-ketone-directed-or-mediated-c-h-functionalization/)
- [Chiral Monophosphorus Ligands for Asymmetric Catalytic Reactions](https://scholariq.org/papers/chiral-monophosphorus-ligands-for-asymmetric-catalytic-reactions/)
- [Rhodium-Catalyzed Asymmetric C–H Functionalization Reactions](https://scholariq.org/papers/rhodium-catalyzed-asymmetric-c-h-functionalization-reactions/)
- [Catalytic C(sp<sup>3</sup>)−H Arylation of Free Primary Amines with an <i>exo</i> Directing Group Generated In Situ](https://scholariq.org/papers/catalytic-c-sp-sup-3-sup-h-arylation-of-free-primary-amines-with-an-i-exo-i/)
- [<i>N</i>-Trifluoromethylthio-dibenzenesulfonimide: A Shelf-Stable, Broadly Applicable Electrophilic Trifluoromethylthiolating Reagent](https://scholariq.org/papers/i-n-i-trifluoromethylthio-dibenzenesulfonimide-a-shelf-stable-broadly-applicable/)
- [Highly Antimalaria‐Active Artemisinin Derivatives: Biological Activity Does Not Correlate with Chemical Reactivity](https://scholariq.org/papers/highly-antimalaria-active-artemisinin-derivatives-biological-activity-does-not/)
- [Facile Synthesis of Chiral α‐Difluoromethyl Amines from <i>N‐</i>(<i>tert</i>‐Butylsulfinyl)aldimines](https://scholariq.org/papers/facile-synthesis-of-chiral-difluoromethyl-amines-from-i-n-i-i-tert-i/)
- [Carbon Dioxide-Mediated C(sp<sup>3</sup>)–H Arylation of Amine Substrates](https://scholariq.org/papers/carbon-dioxide-mediated-c-sp-sup-3-sup-h-arylation-of-amine-substrates/)
- [Decarboxylative acylation of indolines with α-keto acids under palladium catalysis: a facile strategy for the synthesis of 7-substituted indoles](https://scholariq.org/papers/decarboxylative-acylation-of-indolines-with-keto-acids-under-palladium-catalysis/)
- [Merging NiH Catalysis and Inner-Sphere Metal-Nitrenoid Transfer for Hydroamidation of Alkynes](https://scholariq.org/papers/merging-nih-catalysis-and-inner-sphere-metal-nitrenoid-transfer-for/)
- [Hofmann Rearrangement of Carboxamides Mediated by Hypervalent Iodine Species Generated in Situ from Iodobenzene and Oxone: Reaction Scope and Limitations](https://scholariq.org/papers/hofmann-rearrangement-of-carboxamides-mediated-by-hypervalent-iodine-species/)
- [PhI(OCOCF<sub>3</sub>)<sub>2</sub>-Mediated C–C Bond Formation Concomitant with a 1,2-Aryl Shift in a Metal-Free Synthesis of 3-Arylquinolin-2-ones](https://scholariq.org/papers/phi-ococf-sub-3-sub-sub-2-sub-mediated-c-c-bond-formation-concomitant-with-a-1-2/)
- [Ru(II)-Catalyzed Selective C–H Amination of Xanthones and Chromones with Sulfonyl Azides: Synthesis and Anticancer Evaluation](https://scholariq.org/papers/ru-ii-catalyzed-selective-c-h-amination-of-xanthones-and-chromones-with-sulfonyl/)
- [Micellar Catalysis for Ruthenium(II)‐Catalyzed C−H Arylation: Weak‐Coordination‐Enabled C−H Activation in H<sub>2</sub>O](https://scholariq.org/papers/micellar-catalysis-for-ruthenium-ii-catalyzed-c-h-arylation-weak-coordination/)

## Topic primary papers

- [Asymmetric Synthesis of Sulfinamides Using (−)-Quinine as Chiral Auxiliary](https://scholariq.org/papers/asymmetric-synthesis-of-sulfinamides-using-quinine-as-chiral-auxiliary/)
- [Tandem Suzuki Coupling/Intramolecular Oxetane Ring Opening to Form Polycyclic Ring Systems](https://scholariq.org/papers/tandem-suzuki-coupling-intramolecular-oxetane-ring-opening-to-form-polycyclic/)
- [A dual strategy of direct C(sp3)-H sulfonamidation by cross-dehydrogenative coupling and oxidative hydroxylation-condensation](https://scholariq.org/papers/a-dual-strategy-of-direct-c-sp3-h-sulfonamidation-by-cross-dehydrogenative/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.