Stereoselectivity in Organometallic Reactions:  Oxidative Addition of Alkyl Halides to Platinum(II)

1998 ◽  
Vol 17 (13) ◽  
pp. 2805-2818 ◽  
Author(s):  
Cliff R. Baar ◽  
Hilary A. Jenkins ◽  
Jagadese J. Vittal ◽  
Glenn P. A. Yap ◽  
Richard J. Puddephatt
2008 ◽  
pp. 2414 ◽  
Author(s):  
S. Masoud Nabavizadeh ◽  
S. Jafar Hoseini ◽  
Badri Z. Momeni ◽  
Nahid Shahabadi ◽  
Mehdi Rashidi ◽  
...  

2018 ◽  
Vol 37 (15) ◽  
pp. 2450-2467 ◽  
Author(s):  
Ryley Kehoe ◽  
Markshun Mahadevan ◽  
Adeela Manzoor ◽  
Gillian McMurray ◽  
Patrick Wienefeld ◽  
...  

Molecules ◽  
2019 ◽  
Vol 24 (8) ◽  
pp. 1458 ◽  
Author(s):  
Kimihiro Komeyama ◽  
Ryusuke Tsunemitsu ◽  
Takuya Michiyuki ◽  
Hiroto Yoshida ◽  
Itaru Osaka

A direct reductive homo-coupling of alkyl tosylates has been developed by employing a combination of nickel and nucleophilic cobalt catalysts. A single-electron-transfer-type oxidative addition is a pivotal process in the well-established nickel-catalyzed coupling of alkyl halides. However, the method cannot be applied to the homo-coupling of ubiquitous alkyl tosylates due to the high-lying σ*(C–O) orbital of the tosylates. This paper describes a Ni/Co-catalyzed protocol for the activation of alkyl tosylates on the construction of alkyl dimers under mild conditions.


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