scholarly journals Formal Aniline Synthesis from Phenols through Deoxygenative N‐Centered Radical Substitution

2019 ◽  
Vol 25 (67) ◽  
pp. 15267-15271 ◽  
Author(s):  
Samuel W. Lardy ◽  
Kristine C. Luong ◽  
Valerie A. Schmidt
Keyword(s):  
1973 ◽  
Vol 51 (20) ◽  
pp. 3366-3372 ◽  
Author(s):  
Dennis D. Tanner ◽  
Brian G. Brownlee

The photolysis of sulfur monochloride with a series of saturated aliphatic hydrocarbons yielded alkyl chlorides, di- and polysulfides, hydrogen chloride, and elemental sulfur. The free radical substitution reactions leading to the production of alkyl chloride and the di- and polysulfides were shown to proceed via a chlorine atom abstraction reaction. The major products, the di- and polysulfides could be transformed quantitatively, by lithium aluminum hydride reduction into their corresponding mercaptans. The reaction describes a simple free radical route to the synthesis of a variety of alkyl mercaptans.


ChemInform ◽  
2010 ◽  
Vol 27 (6) ◽  
pp. no-no
Author(s):  
L. DESAUBRY ◽  
J.-J. BOURGUIGNON
Keyword(s):  

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