Infrared studies of complexes between carboxylic acids and tertiary amines in argon matrices

Author(s):  
Maria Wierzejewska-Hnat ◽  
Zofia Mielke ◽  
Henryk Ratajczak
ChemInform ◽  
2015 ◽  
Vol 46 (8) ◽  
pp. no-no
Author(s):  
Biquan Xiong ◽  
Longzhi Zhu ◽  
Xiaofeng Feng ◽  
Jian Lei ◽  
Tieqiao Chen ◽  
...  

Author(s):  
Ya. L. Gol'dfarb ◽  
R. M. Ispiryan ◽  
L. I. Belen'kii

2014 ◽  
Vol 2014 (20) ◽  
pp. 4244-4247 ◽  
Author(s):  
Biquan Xiong ◽  
Longzhi Zhu ◽  
Xiaofeng Feng ◽  
Jian Lei ◽  
Tieqiao Chen ◽  
...  

2020 ◽  
Vol 22 (14) ◽  
pp. 5517-5521 ◽  
Author(s):  
Zhaohui Li ◽  
Long Liu ◽  
Kaiqiang Xu ◽  
Tianzeng Huang ◽  
Xinyi Li ◽  
...  

1949 ◽  
Vol 71 (2) ◽  
pp. 575-576 ◽  
Author(s):  
Ralph A. Zingaro ◽  
Judson E. Goodrich ◽  
Jacob. Kleinberg ◽  
Calvin A. VanderWerf

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Zhao Wu ◽  
Samuel N. Gockel ◽  
Kami L. Hull

AbstractPhotoredox catalysis is a powerful means to generate odd-electron species under mild reaction conditions from a wide array of radical precursors. Herein, we present the application of this powerful catalytic manifold to address the hydroalkylation and hydroaminoalkylation of electronically diverse vinylarenes. This reaction allows for generalized alkene hydroalkylation leveraging common alkyl radical precursors, such as organotrifluoroborate salts and carboxylic acids. Furthermore, utilizing easily accessible α-silyl amine reagents or tertiary amines directly, secondary and tertiary amine moieties can be installed onto monoaryl and diaryl alkenes to access valuable products, including γ,γ-diarylamines pharmacophores. Thus, under a unified system, both hydroalkylation and hydroaminoalkylation of alkenes are achieved. The substrate scope is evaluated through 57 examples, the synthetic utility of the method is demonstrated, and preliminary mechanistic insights are presented.


1969 ◽  
Vol 73 (7) ◽  
pp. 2153-2157 ◽  
Author(s):  
J. F. Wojcik ◽  
T. H. Stock

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