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1.
Base-induced chemiluminescent decomposition of bicyclic dioxetanes bearing a (benzothiazol-2-yl)-3-hydroxyphenyl group: a radiationless pathway leading to marked decline of chemiluminescence efficiency.
J Org Chem
; 77(10): 4725-31, 2012 May 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-22524301
2.
Intramolecular charge-transfer-induced decomposition promoted by an aprotic polar solvent for bicyclic dioxetanes bearing a 4-(benzothiazol-2-yl)-3-hydroxyphenyl moiety.
J Org Chem
; 76(3): 902-8, 2011 Feb 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-21192637
3.
Thermodynamic aspects of thermal decomposition and charge-transfer-induced chemiluminescent decomposition for bicyclic dioxetanes bearing a 4-(benzothiazol-2-yl)-3-hydroxyphenyl moiety.
J Org Chem
; 75(11): 3678-84, 2010 Jun 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-20455570
4.
Synthesis of thermally stable acylamino-substituted bicyclic dioxetanes and their base-induced chemiluminescent decomposition.
J Org Chem
; 75(17): 5920-6, 2010 Sep 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-20681740
5.
Marked difference in fragmentation between collision-induced excitation and chemi-excitation of keto esters produced from dioxetanes bearing a 4-(benzothiazol-2-yl)-3-hydroxyphenyl moiety in negative-mode matrix-assisted laser desorption/ionization time-of-flight tandem mass spectrometry.
Rapid Commun Mass Spectrom
; 24(18): 2715-22, 2010 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-20814977
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