Efficient Synthesis of β‐Amino Alcohols Catalyzed by Niobium Pentachloride: Regioselective Ring Opening of Epoxides with Aromatic Amines

2006 ◽  
Vol 36 (21) ◽  
pp. 3183-3189 ◽  
Author(s):  
A. Venkat Narsaiah ◽  
D. Sreenu ◽  
K. Nagaiah
2007 ◽  
Vol 2 (2) ◽  
pp. 1934578X0700200
Author(s):  
Suchitra Bhatt ◽  
Sandip K. Nayak

Anhydrous titanium(III) chloride was found to be a simple and efficient Lewis acid catalyst for ring opening of epoxides at ambient temperature. The reaction proceeded smoothly with anilines as well as azide ion as nucleophiles to give the corresponding β-amino alcohols and β-azido alcohols in moderate to good yields.


ChemInform ◽  
2006 ◽  
Vol 37 (32) ◽  
Author(s):  
M. Mujahid Alam ◽  
Ravi Varala ◽  
Ramu Enugala ◽  
Srinivas R. Adapa

2008 ◽  
Vol 2008 (4) ◽  
pp. 220-221 ◽  
Author(s):  
Dadkhoda Ghazanfari ◽  
Mohammed M. Hashemi ◽  
Mohammad Mehdi Mottaghi ◽  
Mohammad Mehdi Foroughi

2001 ◽  
Vol 25 (2) ◽  
pp. 221-222 ◽  
Author(s):  
L. Rajender Reddy ◽  
M. Arjun Reddy ◽  
N. Bhanumathi ◽  
K. Rama Rao

2004 ◽  
Vol 34 (4) ◽  
pp. 727-734 ◽  
Author(s):  
N. Raghavendra Swamy ◽  
T. Venkateshwar Goud ◽  
S. Malla Reddy ◽  
P. Krishnaiah ◽  
Y. Venkateswarlu

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