Mechanisms of the PtCl2-Catalyzed Intramolecular Cyclization of o-Isopropyl-Substituted Aryl Alkynes for the Synthesis of Indenes and Comparison of Three sp3 C–H Bond Activation Modes

2014 ◽  
Vol 79 (12) ◽  
pp. 5684-5696 ◽  
Author(s):  
Yi Wang ◽  
Wei Liao ◽  
Genping Huang ◽  
Yuanzhi Xia ◽  
Zhi-Xiang Yu
2020 ◽  
Vol 257 (12) ◽  
pp. 2000296
Author(s):  
Mikhail Feofanov ◽  
Vladimir Akhmetov ◽  
Konstantin Amsharov
Keyword(s):  

2015 ◽  
Vol 51 (36) ◽  
pp. 7685-7688 ◽  
Author(s):  
Shunsuke Sueki ◽  
Yoichiro Kuninobu

We successfully developed rhodium-catalysed synthesis of multi-substituted silylindenes from 2 equivalents of aryl alkynes and 1 equivalent of hydrosilanes in moderate to good yields via C–H bond activation for the first time.


2014 ◽  
Vol 50 (18) ◽  
pp. 2350-2352 ◽  
Author(s):  
Neeraj Kumar Mishra ◽  
Jihye Park ◽  
Satyasheel Sharma ◽  
Sangil Han ◽  
Mirim Kim ◽  
...  

The rhodium-catalyzed oxidative alkenylation of N-benzyltriflamides with olefins followed by an intramolecular cyclization via C–H bond activation is described.


2009 ◽  
Vol 48 (22) ◽  
pp. 3999-4001 ◽  
Author(s):  
Shangdong Yang ◽  
Zigang Li ◽  
Xing Jian ◽  
Chuan He

2013 ◽  
Vol 42 (10) ◽  
pp. 1257-1259 ◽  
Author(s):  
Ning-hui Chang ◽  
Hiroki Mori ◽  
Xi-chao Chen ◽  
Yasuhiro Okuda ◽  
Takeru Okamoto ◽  
...  

2009 ◽  
Vol 121 (22) ◽  
pp. 4059-4061 ◽  
Author(s):  
Shangdong Yang ◽  
Zigang Li ◽  
Xing Jian ◽  
Chuan He

2019 ◽  
Vol 17 (10) ◽  
pp. 2725-2733 ◽  
Author(s):  
Yang Yuan ◽  
Hailu Tan ◽  
Lingkai Kong ◽  
Zhong Zheng ◽  
Murong Xu ◽  
...  

Atom-economical synthesis of tetrasubstituted furans from α-aryl ketones and alkynones through base-promoted cleavage of unstrained C–C single bonds of ketones and subsequent Zn-catalyzed cyclization.


2019 ◽  
Vol 43 (25) ◽  
pp. 9961-9968
Author(s):  
Badr Jismy ◽  
Mohamed Akssira ◽  
Damijan Knez ◽  
Gérald Guillaumet ◽  
Stanislav Gobec ◽  
...  

Fluoromethylated imidazo[1,2-a]pyrimidines and benzimidazo[1,2-a]pyrimidines were synthesized through Michael addition/intramolecular cyclization reaction by condensation of 2-amino imidazole derivatives with ethyl 4,4,4-trifluorobut-2-ynate and using C–O bond activation.


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