ChemInform Abstract: Extrusion of CO from Aryl Ketones: Rhodium(I)-Catalyzed C-C Bond Cleavage Directed by a Pyridine Group.

ChemInform ◽  
2012 ◽  
Vol 43 (29) ◽  
pp. no-no
Author(s):  
Zhi-Quan Lei ◽  
Hu Li ◽  
Yang Li ◽  
Xi-Sha Zhang ◽  
Kang Chen ◽  
...  
2012 ◽  
Vol 51 (11) ◽  
pp. 2690-2694 ◽  
Author(s):  
Zhi-Quan Lei ◽  
Hu Li ◽  
Yang Li ◽  
Xi-Sha Zhang ◽  
Kang Chen ◽  
...  

2012 ◽  
Vol 124 (11) ◽  
pp. 2744-2748 ◽  
Author(s):  
Zhi-Quan Lei ◽  
Hu Li ◽  
Yang Li ◽  
Xi-Sha Zhang ◽  
Kang Chen ◽  
...  

2019 ◽  
Vol 84 (18) ◽  
pp. 11823-11838 ◽  
Author(s):  
Popuri Sureshbabu ◽  
Sadaf Azeez ◽  
Nalluchamy Muniyappan ◽  
Shahulhameed Sabiah ◽  
Jeyakumar Kandasamy

RSC Advances ◽  
2016 ◽  
Vol 6 (27) ◽  
pp. 22749-22753 ◽  
Author(s):  
Pochampalli Sathyanarayana ◽  
Atul Upare ◽  
Owk Ravi ◽  
Prathap Reddy Muktapuram ◽  
Surendar Reddy Bathula

Iodine-catalyzed, aerial oxygen supported C–C bond cleavage reaction of aryl alkyl ketones for the synthesis of benzoic acids and benzamides. Also benzylidene acetones and phenylacetylenes were converted to their aromatic acids at this conditions.


2008 ◽  
Vol 693 (26) ◽  
pp. 3939-3942 ◽  
Author(s):  
Kyoji Tsuchikama ◽  
Mitsugu Kasagawa ◽  
Yu-Ki Hashimoto ◽  
Kohei Endo ◽  
Takanori Shibata
Keyword(s):  

ChemInform ◽  
2016 ◽  
Vol 47 (28) ◽  
Author(s):  
Pochampalli Sathyanarayana ◽  
Atul Upare ◽  
Owk Ravi ◽  
Prathap Reddy Muktapuram ◽  
Surendar Reddy Bathula

2018 ◽  
Vol 140 (2) ◽  
pp. 586-589 ◽  
Author(s):  
Tian-Tian Zhao ◽  
Wen-Hua Xu ◽  
Zhao-Jing Zheng ◽  
Peng-Fei Xu ◽  
Hao Wei
Keyword(s):  

2020 ◽  
Vol 2020 (11) ◽  
pp. 1620-1628 ◽  
Author(s):  
Yuqi Zhang ◽  
Zijia Wang ◽  
Zhao Tang ◽  
Zhongfeng Luo ◽  
Hongxiang Wu ◽  
...  

2015 ◽  
Vol 2 (7) ◽  
pp. 765-770 ◽  
Author(s):  
Wen Ding ◽  
Qiuling Song

Chemoselective cleavage of the C(CO)–C(alkyl) bond in aryl ketones leading to azole amides is disclosed. Aryl ketones with a variety of long-chain alkyl groups have been demonstrated to be active substrates and mechanism studies suggested that molecular oxygen serves both as an oxidant and a reactant in this strategy.


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