Gas-phase Diels-Alder reaction of the o-quinodimethane radical cation and neutral styrene

1983 ◽  
Vol 48 (9) ◽  
pp. 1522-1527 ◽  
Author(s):  
Edward K. Chess ◽  
Ping Huang Lin ◽  
Michael L. Gross
2013 ◽  
Vol 32 (11) ◽  
pp. 3385-3390 ◽  
Author(s):  
Hezhi Sun ◽  
Yunfeng Chai ◽  
Lin Wang ◽  
Kezhi Jiang ◽  
Yuanjiang Pan

1999 ◽  
Vol 121 (28) ◽  
pp. 6730-6736 ◽  
Author(s):  
Udo Haberl ◽  
Olaf Wiest ◽  
Eberhard Steckhan

1991 ◽  
Vol 26 (7) ◽  
pp. 669-670 ◽  
Author(s):  
David J. Burinsky ◽  
Richard Dunphy ◽  
J. Douglas Alvessantana ◽  
Mary Lou Cotter

Molecules ◽  
1997 ◽  
Vol 2 (12) ◽  
pp. 80-86 ◽  
Author(s):  
David Rusterholz ◽  
David Gorman ◽  
Paul Gassman

1989 ◽  
Vol 42 (10) ◽  
pp. 1813 ◽  
Author(s):  
LK Dyall

Electron-impact fragmentation of 2-R-4H-3,1-benzoxazin-4-ones involves primary losses of CO2 and R; there is also loss of ketene when R is methyl. The ion RCO+ is a major daughter. Successive losses of CO2and RCN yield an ion m/z 76 formulated as dehydrobenzene radical cation. In the case of 2-methyl-4H-3,1-naphth[2,3-d]oxazin-4-one, the 2,3-dehydronaphthalene ion is produced efficiently, and linked scans (B/E) were used to demonstrate that it loses C4H2 ( diacetylene ) in a retro Diels-Alder reaction.


2018 ◽  
Vol 59 (36) ◽  
pp. 3361-3364 ◽  
Author(s):  
Kenta Tanaka ◽  
Mami Kishimoto ◽  
Mayumi Sukekawa ◽  
Yujiro Hoshino ◽  
Kiyoshi Honda

ChemInform ◽  
2010 ◽  
Vol 22 (29) ◽  
pp. no-no
Author(s):  
A. W. GIESELER ◽  
E. STECKHAN ◽  
O. WIEST ◽  
F. KNOCH

2018 ◽  
Vol 14 ◽  
pp. 642-647 ◽  
Author(s):  
Yasushi Imada ◽  
Yohei Okada ◽  
Kazuhiro Chiba

Single electron transfer (SET)-triggered radical ion-based reactions have proven to be powerful options in synthetic organic chemistry. Although unique chain processes have been proposed in various photo- and electrochemical radical ion-based transformations, the turnover number, also referred to as catalytic efficiency, remains unclear in most cases. Herein, we disclose our investigations of radical cation chain processes in the electrocatalytic Diels–Alder reaction, leading to a scalable synthesis. A gram-scale synthesis was achieved with high current efficiency of up to 8000%. The reaction monitoring profiles showed sigmoidal curves with induction periods, suggesting the involvement of intermediate(s) in the rate determining step.


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