Facile and Selective Synthesis of 2-Substituted Benzimidazoles
293
Acknowledgment
We thank Natural Science Foundation of Hebei Province (B2011201072), National Natural
Science Foundation of China (20806018), the Science Project of the Hebei Education
Department (ZD200910) and Foundation of Hebei University (2009-163).
References
1
2
3
.
.
.
Hirashima S, Suzuki T, Ishida T, Noji S, Ando I, Komatsu M, Ikede S and Hashimoto
H, J Med Chem., 2006, 49, 4721.
Roth T, Morningstar M L, Boyer P L, Hughes S H, Buckheit R W Jr and Michejda C
J, J Med Chem., 1997, 40, 4199.
Migawa M T, Girardet J L, Walker J A, Koszalka G W, Chamberlain S D, Drach J C
and Townsend L B, J Med Chem., 1998, 41, 1242.
Tamm I, Science, 1954, 120, 847.
Wright J B, Chem Rev., 1951, 48, 397.
Fairley T A, Tidwell R R, Donkor I, Naiman N A, Ohemeng K A, Lombardy R J,
Bentley J A and Cory M, J Med Chem., 1993, 36, 1746.
4
5
6
.
.
.
7
8
.
.
Bougrin K, Loupy A and Soufiaoui M, Tetrahedron, 1998, 54, 8055.
Chakrabarty M, Karmakar S, Mukherji A, Arima S and Harigaya Y, Heterocycl.,,
2
006, 68, 967.
Gogoi P and Konwar D, Tetrahedron Lett., 2006, 47, 79.
9
1
1
1
1
1
1
1
1
1
1
2
2
2
.
0. Trivedi R, De S K and Gibbs R A, J Mol Cat A: Chem., 2006, 245, 8.
1. Nagata K, Itoh T, Ishikawa H and Ohsawa A, Heterocycl., 2003, 61, 93.
2. Kawashita Y, Nakamichi N, Kawabata H and Hayashi M, Org Lett., 2003, 5, 3713.
3. Singh M P, Sasmal S, Lu W and Chatterjee M N, Synthesis, 2000, 1380.
4. Bahrami K, Khodaei M M and Kavianinia I, Synthesis, 2007, 547.
5. Das B, Kanth B S, Reddy K R and Kumar A S, J Heterocycl Chem., 2008, 45, 1499.
6. Lee K J and Janda K D, Can J Chem., 2001, 79, 1556.
7. Sharghi H, Asemani O and Khalifeh R, Synth Commun., 2008, 38, 1128.
8. Ma H Q, Wang Y L, Li J P and Wang J Y, Heterocycles, 2007, 71, 135.
9. Das B, Holla H and Srinivas Y, Tetrahedron Lett., 2007, 48, 61.
0. Du L H and Wang Y G, Synthesis, 2007, 675.
1. Lin S N and Yang L H, Tetrahedron Lett., 2005, 46, 4315.
2. Chari M A, Shobha D, Kenawy E R, Al-Deyab S S, Subba Reddy B V and Vinu
Ajayan, Tetrahedron Lett., 2010, 51, 5195.
2
2
2
2
3. Ruiz V R, Corma A and Sabater M J, Tetrahedron, 2010, 66, 730.
4. Gadekar L S, Arbad B R and Lande M K, Chin Chem Lett., 2010, 21, 1053.
5. Speier G and Parkanyi L, J Org Chem., 1986, 51, 218.
6. Ouyang J, Ouyang C G, Fujii Y, Nakano Y, Shoda T and Nagano T, J Heterocycl
Chem., 2004, 41, 359.
2
2
2
3
7. Alloum A B, Bougrin K and Soufiaoui M, Tetrahedron Lett., 2003, 44, 5935.
8. Bahrami K, Khodaei M M and Nejati A, Green Chem., 2010, 12, 1237.
9. Bergbreiter D E and Lalonde J J, J Org Chem., 1987, 52, 1601.
0. Jiang Y, Wang J Y, Chen J H, Wang W J, Yan H, Zhang X X, Wang C, Zhang G L
and Li B G, Acta Chim Sinica, 2007, 65, 1925.
3
1. Li T S, Duan H Y, Li B Z, Tewari B B and Li S H, J Chem Soc., Perkin Trans 1,
1
999, 1, 291.
3
2. Salavati-Niasari M, Hasanalian J and Najafian H, J Mol Catal A: Chem., 2004, 209, 209.
3. Shi J H, Zhou L, Wang L Z and Yan W, J Zhejiang Univ Tech., 2006, 34, 360.
3