Anti‐Markovnikov Addition of Anilines to Aliphatic Terminal Alkynes Catalyzed by an 8‐Quinolinolato Rhodium Complex

Author(s):  
Yoshihiko Morimoto ◽  
Takuya Kochi ◽  
Fumitoshi Kakiuchi
2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Basudeb Basu ◽  
Kinkar Biswas ◽  
Samir Kundu ◽  
Debasish Sengupta

On-water hydrothiolation reaction between terminal alkyne and thiol has been probed in the presence of various additives. Aromatic alkynes yield corresponding 1-alkenyl sulfides, whereas aliphatic alkynes undergo double-addition yielding vicinal disulfides in good to excellent yields. Formation of 1-alkenyl sulfides proceeds with a high degree of regioselectivity (via anti-Markovnikov addition), and switching the stereoselectivity between E/Z isomers has been noticeably realized in the presence of different additives/promoters.


2013 ◽  
Vol 19 (36) ◽  
pp. 12067-12076 ◽  
Author(s):  
Siping Wei ◽  
Julia Pedroni ◽  
Antje Meißner ◽  
Alexandre Lumbroso ◽  
Hans-Joachim Drexler ◽  
...  

2009 ◽  
Vol 74 (24) ◽  
pp. 9433-9439 ◽  
Author(s):  
Taigo Kashiwabara ◽  
Kouichirou Fuse ◽  
Takeshi Muramatsu ◽  
Masato Tanaka

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