ChemInform Abstract: Copper-Catalyzed Tandem Process: An Efficient Approach to 2-Substituted-1,4-benzodioxanes.

ChemInform ◽  
2010 ◽  
Vol 41 (44) ◽  
pp. no-no
Author(s):  
Yunyun Liu ◽  
Weiliang Bao
2015 ◽  
Vol 51 (92) ◽  
pp. 16483-16485 ◽  
Author(s):  
Xiaolin Pan ◽  
Yong Luo ◽  
Hong-Guang Xia ◽  
Jie Wu

An efficient approach for the generation of benzo[b]naphtho[2,3-d]oxocin-6-ones through a palladium-catalyzed tandem reaction of 2-alkynylphenol with 2-(2-bromobenzylidene)cyclobutanone is described. This tandem process afforded the fused polycycles easily, with the formation of three bonds with high efficiency and excellent selectivity.


2021 ◽  
Vol 6 (3) ◽  
pp. 154-160
Author(s):  
Bhima Sridevi

An efficient approach for the formation of biologically important indolo[2,1-b]quinazoline-6,12-diones in good to moderate yields has been accomplished from 2-haloacetophenones and anthranilamides employing I2/DMSO/CuI under aerobic conditions. This tandem process is believed to proceed via iodination of 2-haloacetophenone followed by Kornblum oxidation and copper-catalyzed intramolecular N-arylation. This method adopts five reactions such as α-halogenation, oxidation, condensation, aromatization and heteroaryl coupling in a single step which makes it as an attractive and useful for the synthesis of indolo[2,1-b]quinazoline-6,12-diones.


AIAA Journal ◽  
1998 ◽  
Vol 36 ◽  
pp. 2005-2012
Author(s):  
L. He ◽  
W. Ning

2020 ◽  
Author(s):  
Lucien Caspers ◽  
Julian Spils ◽  
Mattis Damrath ◽  
Enno Lork ◽  
Boris Nachtsheim

In this article we describe an efficient approach for the synthesis of cyclic diaryliodonium salts. The method is based on benzyl alcohols as starting materials and consists of an Friedel-Crafts-arylation/oxidation sequence. Besides a deep optimization, particluar focusing on the choice and ratios of the utilized Bronsted-acids and oxidants, we explore the substrate scope of this transformation. We also discuss an interesting isomerism of cyclic iodonium salts substituted with aliphatic substituents at the bridge head carbon. <br>


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