Rh(III)-Catalyzed, N -Amino-Directed C–H Coupling with α-Cyano-α-Diazoesters for the Synthesis of 3-Aminocinnoline-4-Carboxylates
Year: 2025
Type: article
Abstract: Reactivity-propagating synthesis is proposed herein as a transformative synthetic practice, with both reactant reactivity and product inner reactivity programmed into the synthetic design and survival of product inner reactivity as the central goal. Rh(III)-catalyzed, N -amino-directed C–H coupling with α-cyano-α-diazoesters has been developed for the synthesis of 3-aminocinnoline-4-carboxylates. This synthetic methodology features the survival of the product inner reactivity of two heteroatom sites of nitrogen as well as amino and ester groups, allowing versatile entry into varied open-chain and ring topology structures.
Source: The Journal of Organic Chemistry
Institution: Nanjing University
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: green
Awards: G117299061, G2814365926, G6916446599
OpenAlex ID: W4415313861
