Site‐Selective N‐1 and C‐3 Heteroarylation of Indole with Het‐eroarylnitriles by Organocatalysis under Visible Light

Author(s):  
Li-Zhu Wu ◽  
Chao Zhou ◽  
Qi-Chao Gan ◽  
Tai-Ping Zhou ◽  
Tao Lei ◽  
...  
Keyword(s):  
2021 ◽  
Vol 23 (7) ◽  
pp. 2756-2762
Author(s):  
Jianjing Yang ◽  
Zongzhao Sun ◽  
Kelu Yan ◽  
Haozhe Dong ◽  
Hongyan Dong ◽  
...  

A single-atom photocatalyst Ni/TiO2 was developed for the visible-light-induced site-selective sulfonation of enamides to give amidosulfones with 36 examples up to 99% yield.


2011 ◽  
Vol 1342 ◽  
Author(s):  
Nathaniel Woodward ◽  
Atsushi Nishikawa ◽  
Yasufumi Fujiwara ◽  
Volkmar Dierolf

ABSTRACTWe report site-selective studies of the Zeeman splittings that are observed for magnetic fields up to 6.6T for different Eu incorporation sites in GaN. Utilizing resonant excitation with visible light, we are able to distinguish the site and find for one center (Eu1) a splitting into five components as expected for C3v symmetry. The corresponding g-values are 1.66 and 1.90. The two lines of another center Eu2 each split into two levels corresponding to g-values of 1.9 and 2.84. Most surprisingly a third center, for which only one line is clearly identified, a g-value of 6.16 is found which is larger than can be explained for a 7F2 purely ionic Eu state.


2018 ◽  
Vol 5 (8) ◽  
pp. 1312-1319 ◽  
Author(s):  
Lili Shi ◽  
Hongxin Liu ◽  
Luqiong Huo ◽  
Yaqian Dang ◽  
Yu Wang ◽  
...  

Site-selective phenol acylation mediated by thioacids via photoredox catalysis is described. This protocol provided facile access to an array of phenolic esters with exclusive acylation priority of phenol hydroxyl group to alcoholic one. Its utility was also demonstrated by the modification of biologically meaningful natural product.


Synthesis ◽  
2019 ◽  
Vol 51 (23) ◽  
pp. 4425-4433
Author(s):  
Yong Jian ◽  
Ming Chen ◽  
Chao Yang ◽  
Wujiong Xia

A small molecule, namely nitroacenaphthene, is reported for the first time as a recyclable visible-light photocatalyst for the construction of the C=N bond from sulfonyl azides and amines. This scalable, site-selective protocol provides a convenient way to access various sulfonyl amidines under mild conditions. Two reaction pathways are proposed, according to different transformation patterns.


2020 ◽  
Vol 7 (9) ◽  
pp. 1095-1106
Author(s):  
Damoder Reddy Motati ◽  
Dilipkumar Uredi ◽  
Amarender Goud Burra ◽  
J. Phillip Bowen ◽  
Frank R. Fronczek ◽  
...  

A highly efficient, site-selective, visible light-accelerated, remote C–H halogenation of unsymmetrical aromatic bisamides/amidoesters has been developed.


2010 ◽  
Vol 97 (1-2) ◽  
pp. 115-119 ◽  
Author(s):  
Naoya Murakami ◽  
Asami Ono ◽  
Misa Nakamura ◽  
Toshiki Tsubota ◽  
Teruhisa Ohno
Keyword(s):  

2009 ◽  
Vol 92 (1-2) ◽  
pp. 56-60 ◽  
Author(s):  
Naoya Murakami ◽  
Yuichi Fujisawa ◽  
Toshiki Tsubota ◽  
Teruhisa Ohno

2020 ◽  
Vol 22 (18) ◽  
pp. 7284-7289 ◽  
Author(s):  
Jingya Yang ◽  
Jiaokui Duan ◽  
Ganggang Wang ◽  
Hongyan Zhou ◽  
Ben Ma ◽  
...  
Keyword(s):  

Synthesis ◽  
2020 ◽  
Vol 52 (15) ◽  
pp. 2171-2189
Author(s):  
Kounosuke Oisaki ◽  
Motomu Kanai ◽  
Kentaro Sakai

The development of catalyst-controlled, site-selective C(sp3)–H functionalization reactions is currently a major challenge in organic synthesis. In this paper, a novel bond-weakening catalyst that recognizes the hydroxy group of alcohols through formation of a borate is described. An electron-deficient borinic acid–ethanolamine complex enhances the chemical yield of the α-C–H alkylation of alcohols when used in conjunction with a photoredox catalyst and a hydrogen atom transfer catalyst under irradiation with visible light. This ternary hybrid catalyst system can, for example, be applied to functional-group-enriched­ peptides.


Sign in / Sign up

Export Citation Format

Share Document