An Oxidant- and Catalyst-Free Electrooxidative Cross-Coupling Approach to 3-Tetrahydroisoquinoline Substituted Coumarins

2021 ◽  
Author(s):  
Yanyan Kong ◽  
Jung Keun Kim ◽  
Yabo Li ◽  
Jianye Zhang ◽  
Mengmeng Huang ◽  
...  

A direct electrooxidative cross-dehydrogenative-coupling (CDC) reaction between N-aryl-tetrahydroisoquinolines and 4-hydroxycoumarins has been developed. This protocol provides a green, mild and fast method to construct 3-tetrahydroisoquinoline substituted coumarins in the absence...

RSC Advances ◽  
2014 ◽  
Vol 4 (92) ◽  
pp. 50795-50800 ◽  
Author(s):  
Kammari Bal Raju ◽  
Bejjanki Naveen Kumar ◽  
Kommu Nagaiah

We demonstrated a dehydrogenative cross coupling between a benzyl alcohol and C(sp3)–H bond for the construction of a C–O bond. This method reveals a new strategy for the direct use of benzyl alcohols in the synthesis of esters with the use of copper as a catalyst and TBHP as an oxidant.


2020 ◽  
Vol 07 ◽  
Author(s):  
Tanmay Chatterjee ◽  
Nilanjana Mukherjee

Abstract: A natural driving force is always working behind the synthetic organic chemists towards the development of ‘green’ synthetic methodologies for the synthesis of useful classes of organic molecules having potential applications. The majority of the essential classes of organic transformations, including C-C and C-X (X = heteroatom) bond-forming crosscoupling reactions, cross dehydrogenative-coupling (CDC) mostly rely on the requirement of transition-metal catalysts and hazardous organic solvents. Hence, the scope in developing green synthetic strategies by avoiding the use of transitionmetal catalysts and hazardous organic solvents for those important and useful classes of organic transformations is very high. Hence, several attempts are made so far. Water being the most abundant, cheap, and green solvent in the world; numerous synthetic methods have been developed in an aqueous medium. In this review, the development of transitionmetal- free green synthetic strategies for various important classes of organic transformations such as C-C and C-X bondforming cross-coupling, cross dehydrogenative-coupling, and oxidative-coupling in an aqueous media is discussed.


2021 ◽  
Author(s):  
F. Wieland Goetzke ◽  
Alexander M. L. Hell ◽  
Lucy van Dijk ◽  
Stephen P. Fletcher

2017 ◽  
Vol 58 (18) ◽  
pp. 1742-1746 ◽  
Author(s):  
Xiaohe Xu ◽  
Pingping Li ◽  
Yingyi Huang ◽  
Chuo Tong ◽  
YiYan Yan ◽  
...  

2012 ◽  
Vol 10 (13) ◽  
pp. 2692 ◽  
Author(s):  
Minsik Min ◽  
Bomi Kim ◽  
Sungwoo Hong

2020 ◽  
Vol 56 (51) ◽  
pp. 7001-7004 ◽  
Author(s):  
Yu Chen ◽  
Yangjian Quan ◽  
Zuowei Xie

Ir-catalyzed highly selective B–H/C–H cross dehydrogenative coupling between o-carboranes and (hetero)aryls has been achieved using a mixed directing-group strategy.


2020 ◽  
Vol 49 (7) ◽  
pp. 809-812
Author(s):  
Tsuneyuki Kobayashi ◽  
Takamitsu Hosoya ◽  
Suguru Yoshida

2019 ◽  
Vol 55 (98) ◽  
pp. 14813-14816 ◽  
Author(s):  
Hao Tian ◽  
Wentao Xu ◽  
Yuxiu Liu ◽  
Qingmin Wang

Herein, we describe a protocol for alkylation reactions of C(sp3)–H bonds with diacyl peroxides by means of a process involving cross-coupling between an alkyl radical and an α-aminoalkyl radical.


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