ritter reaction
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scholarly journals The Serendipitous Effect of KF in Ritter Reaction: Photo-Induced Amino-Alkylation of Alkenes

iScience ◽  
2021 ◽  
pp. 102969
Author(s):  
Yu-Qing Guan ◽  
Xiang-Ting Min ◽  
Gu-Cheng He ◽  
Ding-Wei Ji ◽  
Shi-Yu Guo ◽  
...  
Keyword(s):  
Ritter Reaction

scholarly journals Catalytic Radical-Polar Crossover Ritter Reaction

2021 ◽  
Author(s):  
Eric Touney ◽  
Riley Cooper ◽  
Sarah Bredenkamp ◽  
David George ◽  
Sergey Pronin
Keyword(s):  
Hydrogen Atom ◽  
Hydrogen Evolution ◽  
Functional Groups ◽  
Hydrogen Atom Transfer ◽  
Catalyst Design ◽  
Ritter Reaction ◽  
Organic Reactions ◽  
Atom Transfer ◽  
Substitution Pattern ◽  
Diverse Range

A catalytic radical-polar crossover Ritter reaction is described. The transformation proceeds under acid-free conditions and tolerates a variety of functional groups. The catalyst design overcomes limitations in the substitution pattern of starting materials and enables hydroamidation of a diverse range of alkenes. Formation of hydrogen contributes to the background consumption of reductant and oxidant and competes with the desired pathway, pointing to a mechanistic link between hydrogen atom transfer-initiated organic reactions and hydrogen evolution catalysis.

scholarly journals Catalytic Radical-Polar Crossover Ritter Reaction

2021 ◽  
Author(s):  
Eric Touney ◽  
Riley Cooper ◽  
Sarah Bredenkamp ◽  
David George ◽  
Sergey Pronin
Keyword(s):  
Hydrogen Atom ◽  
Hydrogen Evolution ◽  
Functional Groups ◽  
Hydrogen Atom Transfer ◽  
Catalyst Design ◽  
Ritter Reaction ◽  
Organic Reactions ◽  
Atom Transfer ◽  
Substitution Pattern ◽  
Diverse Range

A catalytic radical-polar crossover Ritter reaction is described. The transformation proceeds under acid-free conditions and tolerates a variety of functional groups. The catalyst design overcomes limitations in the substitution pattern of starting materials and enables hydroamidation of a diverse range of alkenes. Formation of hydrogen contributes to the background consumption of reductant and oxidant and competes with the desired pathway, pointing to a mechanistic link between hydrogen atom transfer-initiated organic reactions and hydrogen evolution catalysis.

Ritter Reaction

2021 ◽  
pp. 471-473
Author(s):  
Jie Jack Li
Keyword(s):  
Ritter Reaction

Tropylium-Promoted Ritter Reactions

2021 ◽  
Author(s):  
Son Hoai Doan ◽  
Mohanad Hussein ◽  
Thanh Vinh Nguyen
Keyword(s):  
Ritter Reaction ◽  
The Ritter Reaction ◽  
Alkyl Amide

The Ritter reaction used to be one of the most powerful synthetic tools to functionalize alcohols and nitriles, providing valuable N-alkyl amide products. However, this reaction has not been frequently...

Recent advances of Ritter reaction and its synthetic applications

2021 ◽  
Author(s):  
Fu-Min Zhang ◽  
Meng-En Chen ◽  
Xiao-Wei Chen ◽  
Yue-Hong Hu ◽  
Rui Ye ◽  
...  
Keyword(s):  
Review Article ◽  
Ritter Reaction ◽  
Present Review ◽  
Recent Advances ◽  
Comprehensive Survey

In comparison to previous reviews, the present review article provides a comprehensive survey of Ritter reactions from 2014 to 2020, mainly aiming to discuss diverse Ritter reactions and their widely...

scholarly journals Ritter-enabled catalytic asymmetric chloroamidation of olefins

2021 ◽  
Author(s):  
Daniel C. Steigerwald ◽  
Bardia Soltanzadeh ◽  
Aritra Sarkar ◽  
Cecilia C. Morgenstern ◽  
Richard J. Staples ◽  
...  
Keyword(s):  
Nitrogen Atom ◽  
Ritter Reaction ◽  
Catalytic Asymmetric

Intermolecular haloamination reactions are challenging due to the high halenium affinity of the nitrogen atom. This is circumvented by using acetonitrile as an attenuated nucleophile, resulting in an enantioselective halo-Ritter reaction.

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