scholarly journals Behavior of o-(alkoxycarbonyl)phenylcarbenes - Reactivity under flash vacuum pyrolysis conditions and observation of reactive intermediates by low temperature matrix isolation technique.

1989 ◽  
pp. 1431-1439 ◽  
Author(s):  
Hideo TOMIOKA ◽  
Yasuki OHTAWA ◽  
Shigeru MURATA
2017 ◽  
Vol 41 (24) ◽  
pp. 15581-15589 ◽  
Author(s):  
Maria I. L. Soares ◽  
Cláudio M. Nunes ◽  
Clara S. B. Gomes ◽  
Teresa M. V. D. Pinho e Melo ◽  
Rui Fausto

The conformational and photochemical behaviour of a 2-(1H-tetrazol-1-yl)thiophene was studied using low-temperature matrix isolation infrared spectroscopy and theoretical calculations. FVP of 2-(1H-tetrazol-1-yl)thiophene afforded new thieno-fused heterocycles.


2004 ◽  
Vol 33 (10) ◽  
pp. 1290-1291 ◽  
Author(s):  
Yoshiko Koizumi ◽  
Shu Seki ◽  
Anjali Acharya ◽  
Akinori Saeki ◽  
Seiichi Tagawa

ChemInform ◽  
2010 ◽  
Vol 22 (18) ◽  
pp. no-no
Author(s):  
V. N. KHABASHESKU ◽  
S. E. BOGANOV ◽  
P. S. ZUEV ◽  
O. M. NEFEDOV ◽  
J. TAMAS ◽  
...  

2014 ◽  
Vol 67 (9) ◽  
pp. 1324 ◽  
Author(s):  
André Korte ◽  
Artur Mardyukov ◽  
Wolfram Sander

The three isomeric pyridyl radicals 2a–c were synthesised using flash vacuum pyrolysis in combination with matrix isolation and characterised by infrared spectroscopy. The IR spectra are in good agreement with spectra calculated using density functional theory methods. The reaction of the pyridyl radicals 2 with molecular oxygen leads to the formation of the corresponding pyridylperoxy radicals 3a–c. The peroxy radicals 3 are photolabile, and irradiation results in syn–anti isomerisation of 3a and 3b and ring expansion of all three isomers of 3.


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