Dynamic 1H NMR Study of Aryl-Nitrogen Single Bond and Carbon-Carbon Double Bond Rotational Energy Barriers in Two Highly Functionalized Pyranopyrimidines

2001 ◽  
Vol 132 (6) ◽  
pp. 683-687 ◽  
Author(s):  
Issa Yavari ◽  
Norollah Hazeri ◽  
Malek T. Maghsoodlou ◽  
Nader Zabarjad-Shiraz
ARKIVOC ◽  
2009 ◽  
Vol 2008 (17) ◽  
pp. 12-19
Author(s):  
Roya Kabiri ◽  
Nourallah Hazeri ◽  
Sayyed Mostafa Habibi Khorassani ◽  
Malek Taher Maghsoodlou ◽  
Ali Ebrahimi ◽  
...  

2009 ◽  
Vol 50 (26) ◽  
pp. 3621-3624 ◽  
Author(s):  
Sayyed Mostafa Habibi-Khorassani ◽  
Malek Taher Maghsoodlou ◽  
Ali Ebrahimi ◽  
Fatemeh Vasheghani Farahani ◽  
Elahe Mosaddeg ◽  
...  

2007 ◽  
Vol 182 (3) ◽  
pp. 647-655 ◽  
Author(s):  
Malek Taher Maghsoodlou ◽  
Sayyed Mostafa Habibi Khorassani ◽  
Uranous Niroumand ◽  
Faramarz Rostami Charati ◽  
Maryam Khosrosharodi

2017 ◽  
Vol 1133 ◽  
pp. 244-252 ◽  
Author(s):  
Fahimeh Movahedifar ◽  
Ali Reza Modarresi-Alam ◽  
Erich Kleinpeter ◽  
Uwe Schilde
Keyword(s):  
1H Nmr ◽  

2011 ◽  
Vol 49 (5) ◽  
pp. 213-220 ◽  
Author(s):  
Sayyed Mostafa Habibi-Khorassani ◽  
Ali Ebrahimi ◽  
Malek Taher Maghsoodlou ◽  
Sara Same-Salari ◽  
Shahin Nasiri ◽  
...  

1971 ◽  
Vol 49 (18) ◽  
pp. 3069-3071 ◽  
Author(s):  
Y. L. Chow ◽  
S. C. Chen ◽  
D. W. L. Chang

The stereochemical course of the photoaddition of nitrosamines to a carbon–carbon double bond was shown to follow a free radical mechanism initiated by aminium radicals. The photoaddition to cyclohexene was highly stereoselective in which the addendum approached in anti-diaxial mode. Similar photoadditions to cis- and trans-2-butenes were less stereoselective, giving mixtures of the erythro- and threo-adducts, owing to the rotation of the carbon-carbon single bond in the intermediate stage.


2002 ◽  
Vol 133 (8) ◽  
pp. 1109-1113 ◽  
Author(s):  
Issa Yavari ◽  
Mehdi Adib ◽  
Hamid R. Bijanzadeh ◽  
Majid M. M. Sadegi ◽  
Hossein Logmani-Khouzani ◽  
...  

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