Electron-Transfer-Initiated Cascade Cyclizations of Terpenoid Polyalkenes in a Low-Polarity Solvent: One-Step Synthesis of Mono- and Polycylic Terpenoids with Various Functionalities

2004 ◽  
Vol 2004 (17) ◽  
pp. 3686-3692 ◽  
Author(s):  
Mustafa E. Ozser ◽  
Huriye Icil ◽  
Yevgeny Makhynya ◽  
Martin Demuth
2003 ◽  
Vol 5 (14) ◽  
pp. 2581-2581
Author(s):  
V. Satish Kumar ◽  
Danielle L. Aubele ◽  
Paul E. Floreancig

2004 ◽  
Vol 43 (7) ◽  
pp. 853-856 ◽  
Author(s):  
Kei Ohkubo ◽  
Hiroaki Kotani ◽  
Jianguo Shao ◽  
Zhongping Ou ◽  
Karl M. Kadish ◽  
...  

2005 ◽  
Vol 8 (8) ◽  
pp. A382 ◽  
Author(s):  
Kentarou Nishi ◽  
Toyohiko Nishiumi ◽  
Masayoshi Higuchi ◽  
Kimihisa Yamamoto

2015 ◽  
Vol 2015 ◽  
pp. 1-13 ◽  
Author(s):  
J. J. Fifen ◽  
Z. Dhaouadi ◽  
M. Nsangou ◽  
O. Holtomo ◽  
N. Jaidane

The distinction of concerted proton-coupled electron transfer (CPCET) from sequential one as well as proton transfer-electron transfer (PT-ET) from electron transfer-proton transfer (ET-PT) in the O–H bond cleavage reactions in various media has always been a difficult task. In this work, the activation barrier of the CPCET mechanism, its rate constants, and reaction free energies related to ET-PT and PT-ET involving coreactive species were presented as good parameters to attempt the problem. DFT calculations were carried out studying the described pathways subsequent to the scavenging of OH• and OBr- by the 3,4-DHPPA in various media. The solvation was described in a hybrid manner using IEF-PCM model conjointly with a model that takes into account some solute-solvent interactions. As a result, we found that the scavenging of hydroxyl radical by 3,4-DHPPA is thermodynamically governed by a one-step hydrogen atom transfer (CPCET) from the acid to the radical in all media. In kinetic viewpoint, CPCET still dominates in the vacuum and in nonpolar solvents, but in polar solvents it could compete strongly with the ET-PT mechanism so that the latter could slightly dominate.


2015 ◽  
Vol 3 (13) ◽  
pp. 6733-6738 ◽  
Author(s):  
Dilshad Masih ◽  
Shawkat M. Aly ◽  
Erkki Alarousu ◽  
Omar F. Mohammed

Herein, we report for the first time the photoinduced triplet-state electron transfer of Pt(ii)TMPyP as an easy, rapid, environmentally friendly, ultra-sensitive and economical method for the determination of iodide in the aqueous phase.


2002 ◽  
Vol 4 (15) ◽  
pp. 2489-2492 ◽  
Author(s):  
V. Satish Kumar ◽  
Danielle L. Aubele ◽  
Paul E. Floreancig

Sign in / Sign up

Export Citation Format

Share Document