NHC-Catalyzed Oxidative Cyclization Reactions of 2-Alkynylbenzaldehydes under Aerobic Conditions: Synthesis of O-Heterocycles

2011 ◽  
Vol 13 (9) ◽  
pp. 2228-2231 ◽  
Author(s):  
Jong Hyub Park ◽  
Sachin V. Bhilare ◽  
So Won Youn
2021 ◽  
Vol 13 (5) ◽  
pp. 6349-6358
Author(s):  
Zainab Almansaf ◽  
Jiyun Hu ◽  
Federica Zanca ◽  
Hamid R. Shahsavari ◽  
Benjamin Kampmeyer ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Chengshuo Shen ◽  
Guoli Zhang ◽  
Yongle Ding ◽  
Na Yang ◽  
Fuwei Gan ◽  
...  

AbstractNanographenes are emerging as a distinctive class of functional materials for electronic and optical devices. It is of remarkable significance to enrich the precise synthetic chemistry for these molecules. Herein, we develop a facile strategy to recompose helicenes into chiral nanographenes through a unique oxidative cyclo-rearrangement reaction. Helicenes with 7~9 ortho-fused aromatic rings are firstly oxidized and cyclized, and subsequently rearranged into nanographenes with an unsymmetrical helicoid shape through sequential 1,2-migrations. Such skeletal reconstruction is virtually driven by the gradual release of the strain of the highly distorted helicene skeleton. Importantly, the chirality of the helicene precursor can be integrally inherited by the resulting nanographene. Thus, a series of chiral nanographenes are prepared from a variety of carbohelicenes and heterohelicenes. Moreover, such cyclo-rearrangement reaction can be sequentially or simultaneously associated with conventional oxidative cyclization reactions to ulteriorly enrich the geometry diversity of nanographenes, aiming at innovative properties.


2020 ◽  
Vol 7 (19) ◽  
pp. 3969-3974
Author(s):  
Qi An ◽  
Chaoyin He ◽  
Xiaodong Fan ◽  
Chuanfu Hou ◽  
Jian Zhao ◽  
...  

Synlett ◽  
2018 ◽  
Vol 29 (13) ◽  
pp. 1717-1722 ◽  
Author(s):  
Manjula Alla ◽  
Gal Potuganti ◽  
Divakar Indukuri

An efficient one-pot synthesis of quinazolino[4,3-b]quinazoline derivatives has been accomplished, starting from 2-(2-bromo­phenyl)quinazolin-4(3H)-one, aldehydes, and various nitrogen sources under aerobic conditions. The multicomponent protocol is mediated by copper(I) salts and involves amination of 2-(2-bromophenyl)quinazolin-4(3H)-one, followed by condensation with the aldehyde and an oxidative cyclization to give the target compounds in moderate to good yields.


ChemInform ◽  
2015 ◽  
Vol 46 (10) ◽  
pp. no-no
Author(s):  
Amy A. van Loon ◽  
Maeve K. Holton ◽  
Catherine R. Downey ◽  
Taryn M. White ◽  
Carly E. Rolph ◽  
...  

2005 ◽  
Vol 7 (16) ◽  
pp. 3553-3556 ◽  
Author(s):  
John D. Brandt ◽  
Kevin D. Moeller

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