[(PPh3)2NiCl2]-Catalyzed C–N Bond Formation Reaction via Borrowing Hydrogen Strategy: Access to Diverse Secondary Amines and Quinolines

Author(s):  
S. N. R. Donthireddy ◽  
Vipin K. Pandey ◽  
Arnab Rit
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Gang Wang ◽  
Ran Lu ◽  
Chuangchuang He ◽  
Lei Liu

AbstractCatalytic kinetic resolution of amines represents a longstanding challenge in chemical synthesis. Here, we described a kinetic resolution of secondary amines through oxygenation to produce enantiopure hydroxylamines involving N–O bond formation. The economic and practical titanium-catalyzed asymmetric oxygenation with environmentally benign hydrogen peroxide as oxidant is applicable to a range of racemic indolines with multiple stereocenters and diverse substituent patterns in high efficiency with efficient chemoselectivity and enantio-discrimination. Late-stage asymmetric oxygenation of bioactive molecules that are otherwise difficult to synthesize was also explored.


Author(s):  
Mamiko Hayakawa ◽  
Hisashi Shirota ◽  
Souta Hirayama ◽  
Ryuusei Yamada ◽  
Tadashi Aoyama ◽  
...  

2021 ◽  
Vol 6 (17) ◽  
pp. 4089-4097
Author(s):  
Ruxin Qu ◽  
Yaxuan Cheng ◽  
Siwei Yang ◽  
Chaoyu Zhao ◽  
Huiling Liu ◽  
...  

ChemInform ◽  
2009 ◽  
Vol 40 (35) ◽  
Author(s):  
G. W. Lamb ◽  
J. M. J. Williams

SynOpen ◽  
2017 ◽  
Vol 01 (01) ◽  
pp. 0001-0007 ◽  
Author(s):  
Meng-Tian Zeng ◽  
Wan Xu ◽  
Min Liu ◽  
Xing Liu ◽  
Cai-Zhu Chang ◽  
...  

A series of 2-aminobenzothiazoles were synthesized by a palladium-catalysed oxidative coupling with good yields (62–89%). Iodobenzene was found to be effective as an additive in this intramolecular C–S bond-formation reaction. The directing thiourea group attached to the aryl ring is essential for the activation of the ortho C–H bond.


1988 ◽  
Vol 53 (12) ◽  
pp. 2683-2687 ◽  
Author(s):  
Tetsuji Kametani ◽  
Shih Der Chu ◽  
Akira Itoh ◽  
Sayuri Maeda ◽  
Toshio Honda

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