scholarly journals Investigations of alkynylbenziodoxole derivatives for radical alkynylations in photoredox catalysis

2018 ◽  
Vol 14 ◽  
pp. 1215-1221 ◽  
Author(s):  
Yue Pan ◽  
Kunfang Jia ◽  
Yali Chen ◽  
Yiyun Chen

The alkynylbenziodoxole derivatives are recently developed alkynylation reagents in organic synthesis, which demonstrate excellent radical alkynylation reactivity in photoredox catalysis reactions. Herein we report the synthesis of alkynylbenziodoxole derivatives with difluoro, monofluoro, monomethoxy, and dimethoxy substitution on the benziodoxole moiety, and investigated their radical alkynylation reactivity for the first time. A series of mechanistic experiments were conducted to study the radical acceptor and oxidative quencher reactivity of alkynylbenziodoxoles, in which unsubstituted alkynylbenziodoxoles played balancing roles in both processes, while electron-rich benziodoxole derivatives demonstrate synthetic advantages in some cases.

2017 ◽  
Vol 4 (7) ◽  
pp. 1331-1335 ◽  
Author(s):  
Shi-Ming Xu ◽  
Jian-Qiang Chen ◽  
Dan Liu ◽  
Yun Bao ◽  
Yong-Min Liang ◽  
...  

Abundant and inexpensive aroyl chlorides have been employed for the first time as novel acyl radical precursors in visible-light photocatalysis.


Author(s):  
Vishal Srivastava ◽  
Pravin Kumar Singh ◽  
Shraddha Tivari ◽  
Praveen Pratap Singh

Visible light and photoredox catalysis have emerged as a powerful and long-lasting tool for organic synthesis, demonstrating the importance of a variety of chemical bond formation methods. Natural products, physiologically...


2016 ◽  
Vol 52 (3) ◽  
pp. 481-484 ◽  
Author(s):  
Bo Chen ◽  
Sensen Shang ◽  
Lianyue Wang ◽  
Yi Zhang ◽  
Shuang Gao

Mesoporous carbon derived from natural vitamin B12 is applied for the first time in organic synthesis and exhibits exceptionally high dual activity for imine formation via the cross-coupling of alcohols with amines and the self-coupling of primary amines.


2019 ◽  
Vol 10 (12) ◽  
pp. 1431-1441 ◽  
Author(s):  
Patxi Garra ◽  
Damien Brunel ◽  
Guillaume Noirbent ◽  
Bernadette Graff ◽  
Fabrice Morlet-Savary ◽  
...  

Ferrocene-based photoredox catalysis is proposed here for the first time.


2012 ◽  
Vol 8 ◽  
pp. 1936-1998 ◽  
Author(s):  
Henning Hopf ◽  
Georgios Markopoulos

This review describes the preparation, structural properties and the use of bisallenes in organic synthesis for the first time. All classes of compounds containing at least two allene moieties are considered, starting from simple conjugated bisallenes and ending with allenes in which the two cumulenic units are connected by complex polycyclic ring systems, heteroatoms and/or heteroatom-containing tethers. Preparatively the bisallenes are especially useful in isomerization and cycloaddition reactions of all kinds leading to the respective target molecules with high atom economy and often in high yield. Bisallenes are hence substrates for generating molecular complexity in a small number of steps (high step economy).


2019 ◽  
Vol 4 (12) ◽  
Author(s):  
Indrajit Ghosh

Abstract Over the last decade, visible light photocatalysis has dramatically increased the arsenal of methods for organic synthesis and changed the way we activate molecules for chemical reactions. Polypyridyl transition metal complexes, redox-active organic dyes, and inorganic semiconductors are typically used as photocatalysts for such transformations. This chapter reviews the applications of radical anions and anions as photosensitizers in visible light photoredox catalysis.


Molecules ◽  
2019 ◽  
Vol 24 (7) ◽  
pp. 1231 ◽  
Author(s):  
Naliharifetra Ranaivoarimanana ◽  
Kyohei Kanomata ◽  
Takuya Kitaoka

Cellulose nanofibers (CNFs) have recently attracted much attention as catalysts in various reactions. Organocatalysts have emerged as sustainable alternatives to metal-based catalysts in green organic synthesis, with concerted systems containing CNFs that are expected to provide next-generation catalysis. Herein, for the first time, we report that a representative organocatalyst comprising an unexpected combination of 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-oxidized CNFs and proline shows significantly enhanced catalytic activity in an asymmetric Michael addition.


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