Study of the thermochemistry of the ethyl + molecular oxygen .dblharw. ethylperoxy (C2H5O2) and tert-butyl + molecular oxygen .dblharw. tert-butylperoxy (tert-C4H9O2) reactions and of the trend in the alkylperoxy bond strengths

1986 ◽  
Vol 90 (3) ◽  
pp. 402-407 ◽  
Author(s):  
Irene R. Slagle ◽  
Emil Ratajczak ◽  
David Gutman
2013 ◽  
Vol 9 ◽  
pp. 1713-1717 ◽  
Author(s):  
Daisuke Hirose ◽  
Tsuyoshi Taniguchi

Water induces a change in the product of radical multifunctionalization reactions of aliphatic alkenes involving an sp3 C–H functionalization by an 1,5-hydrogen shift using tert-butyl nitrite and molecular oxygen. The reaction without water, reported previously, gives nitrated γ-lactols, whereas the reaction in the presence of water produces 4-hydroxy-5-nitropentyl nitrate or 4-hydroxy-3-nitropentyl nitrate derivatives.


2020 ◽  
Vol 22 (24) ◽  
pp. 9719-9723
Author(s):  
Bo Li ◽  
Ye-Qiang Han ◽  
Xu Yang ◽  
Bing-Feng Shi

Synthesis ◽  
2017 ◽  
Vol 50 (04) ◽  
pp. 711-722 ◽  
Author(s):  
Xiaodong Jia ◽  
Pengfei Li

tert-Butyl nitrite (TBN) is an important metal-free reagent that is widely applied in various organic transformations. Besides its traditional applications in nitrosation and diazotization, its ability to activate molecular oxygen to enable the initiation of radical reactions, including nitration, oximation, oxidation, and so on, has attracted extensively attention in the past decade. This review highlights recent advances in this field to promote further exploration of this versatile compound.1 Introduction2 Reactions Involving TBN2.1 Nitrosation2.2 Oximation2.3 Diazotization2.4 Nitration2.5 Oxidation2.6 Other Reactions3 Conclusion and Perspective


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