Concerted Reaction

2016 ◽  
Author(s):  
Vladimir I. Minkin
Keyword(s):  
1998 ◽  
Vol 17 (13) ◽  
pp. 2825-2831 ◽  
Author(s):  
Kazunari Yoshizawa ◽  
Yoshihito Shiota ◽  
Tokio Yamabe

2001 ◽  
Vol 347 (1-3) ◽  
pp. 268-276 ◽  
Author(s):  
Dieter Cremer ◽  
Elfi Kraka ◽  
Ramon Crehuet ◽  
Josep Anglada ◽  
Jürgen Gräfenstein

2009 ◽  
Vol 915 (1-3) ◽  
pp. 178-181
Author(s):  
Aristophanes Metropoulos
Keyword(s):  

2014 ◽  
Vol 67 (3) ◽  
pp. 320 ◽  
Author(s):  
Werner Fudickar ◽  
Torsten Linker

Herein we describe the recent mechanistic understandings of the singlet oxygen ene reaction to give hydroperoxides and the [4+2] cycloaddition affording endoperoxides. Both experimental findings and theoretical work conclude in the formation of intermediates structurally similar to perepoxides during the ene reaction. Such intermediates mainly control the regio- and stereoselectivities of this reaction class. For the [4+2] cycloaddition, both a synchronous concerted reaction (benzene, naphthalenes) and a stepwise reaction with a non-symmetric zwitterionic intermediate (larger acenes) have been found. The thermolysis of endoperoxides derived from acenes proceeds stepwise for anthracenes, but in a concerted manner for less stable adducts such as naphthalene.


Sign in / Sign up

Export Citation Format

Share Document