Reductive deaminative cross-coupling of alkyl bistriflimides enabled by electrocatalysis DOI Creative Commons
Xiangzhang Tao, Wooseok Lee,

Zhimin Xu

и другие.

Science Advances, Год журнала: 2024, Номер 10(47)

Опубликована: Ноя. 22, 2024

We present a versatile nickel-electrocatalytic deaminative cross-coupling platform for the efficient construction of C(sp 3 )–C(sp ) and 2 bonds from readily available alkyl bistriflimides. This methodology involves assembly two leaving groups on amines to form bistriflimides, followed by their effective coupling with wide range halides, pseudohalides, aryl alkenyl halides under electrochemical reductive conditions. Moreover, successful application relay transition metal–free cross-electrophile further demonstrates versatility bistriflimides as valuable building blocks in organic synthesis. Combined control experiments density functional theory calculations provide insights into reaction pathway crucial role iodide catalytic process.

Язык: Английский

Ni-Catalyzed Electroreductive Decarboxylative Cross-Coupling of Redox-Active Esters and Oxime Esters DOI
Martin Oestreich, Hendrik F. T. Klare, Nektarios Kranidiotis‐Hisatomi

и другие.

Synfacts, Год журнала: 2024, Номер 20(05), С. 0498 - 0498

Опубликована: Апрель 15, 2024

Key words C(sp3)–N coupling - electrochemistry imines nickel catalysis oxime esters redox-active

Язык: Английский

Процитировано

0
Direct catalytic photodecarboxylative amination of carboxylic acids with diazirines for divergent access to nitrogen-containing compounds DOI Creative Commons

Vishala Maharaj,

Paresh R. Athawale,

Preeti P. Chandrachud

и другие.

Cell Reports Physical Science, Год журнала: 2024, Номер 5(8), С. 102103 - 102103

Опубликована: Июль 12, 2024

Язык: Английский

Процитировано

0
Reductive deaminative cross-coupling of alkyl bistriflimides enabled by electrocatalysis DOI Creative Commons
Xiangzhang Tao, Wooseok Lee,

Zhimin Xu

и другие.

Science Advances, Год журнала: 2024, Номер 10(47)

Опубликована: Ноя. 22, 2024

We present a versatile nickel-electrocatalytic deaminative cross-coupling platform for the efficient construction of C(sp 3 )–C(sp ) and 2 bonds from readily available alkyl bistriflimides. This methodology involves assembly two leaving groups on amines to form bistriflimides, followed by their effective coupling with wide range halides, pseudohalides, aryl alkenyl halides under electrochemical reductive conditions. Moreover, successful application relay transition metal–free cross-electrophile further demonstrates versatility bistriflimides as valuable building blocks in organic synthesis. Combined control experiments density functional theory calculations provide insights into reaction pathway crucial role iodide catalytic process.

Язык: Английский

Процитировано

0