-
1
-
-
84858015797
-
Oxadiazoles in medicinal chemistry
-
J. Boström, A. Hogner, A. Llinàs, E. Wellner, and A.T. Plowright Oxadiazoles in medicinal chemistry J. Med. Chem. 55 2012 1817 1830
-
(2012)
J. Med. Chem.
, vol.55
, pp. 1817-1830
-
-
Boström, J.1
Hogner, A.2
Llinàs, A.3
Wellner, E.4
Plowright, A.T.5
-
2
-
-
37449025215
-
One-pot synthesis, antibacterial and antifungal activities of novel 2,5-disubstituted-1,3,4-oxadiazoles
-
A. Rauf, S. Sharma, and S. Gangal One-pot synthesis, antibacterial and antifungal activities of novel 2,5-disubstituted-1,3,4-oxadiazoles Chin. Chem. Lett. 19 2008 5 8
-
(2008)
Chin. Chem. Lett.
, vol.19
, pp. 5-8
-
-
Rauf, A.1
Sharma, S.2
Gangal, S.3
-
3
-
-
44549084086
-
A mild and facile method for one pot synthesis of 2,5-di-substituted-1,3, 4-oxadiazoles at room temperature
-
S. Rostamizadeh, and S. Ghamkhar A mild and facile method for one pot synthesis of 2,5-di-substituted-1,3,4-oxadiazoles at room temperature Chin. Chem. Lett. 19 2008 639 642
-
(2008)
Chin. Chem. Lett.
, vol.19
, pp. 639-642
-
-
Rostamizadeh, S.1
Ghamkhar, S.2
-
4
-
-
52049084123
-
An expeditious and one-pot synthesis of unsymmetrical 2,5-disubstituted-1,3,4-oxadiazoles under microwave irradiation and solvent-free conditions
-
N. Montazeri, and K. Rad-Moghadam An expeditious and one-pot synthesis of unsymmetrical 2,5-disubstituted-1,3,4-oxadiazoles under microwave irradiation and solvent-free conditions Chin. Chem. Lett. 19 2008 1143 1146
-
(2008)
Chin. Chem. Lett.
, vol.19
, pp. 1143-1146
-
-
Montazeri, N.1
Rad-Moghadam, K.2
-
5
-
-
33846911827
-
Synthesis and fungicidal activities of 2-alkylthio-5-(3,4,5- tribenzyloxyphenyl)-1,3,4-oxadiazoles
-
D.Q. Long, D.J. Li, W.Q. Cai, and S.S. Chen Synthesis and fungicidal activities of 2-alkylthio-5-(3,4,5-tribenzyloxyphenyl)-1,3,4-oxadiazoles Chin. Chem. Lett. 17 2006 1427 1430
-
(2006)
Chin. Chem. Lett.
, vol.17
, pp. 1427-1430
-
-
Long, D.Q.1
Li, D.J.2
Cai, W.Q.3
Chen, S.S.4
-
6
-
-
41049111165
-
Solvent-free synthesis of some new 2-(3,5-dimethoxy-4-methylphenyl)-5- aryl-1,3,4-oxadiazoles
-
A. Saeed, and A. Mumtaz Solvent-free synthesis of some new 2-(3,5-dimethoxy-4-methylphenyl)-5-aryl-1,3,4-oxadiazoles Chin. Chem. Lett. 19 2008 423 427
-
(2008)
Chin. Chem. Lett.
, vol.19
, pp. 423-427
-
-
Saeed, A.1
Mumtaz, A.2
-
7
-
-
84855926456
-
High-temperature continuous flow synthesis of 1,3,4-oxadiazoles via N-acylation of 5-substituted tetrazoles
-
B. Reichart, and C.O. Kappe High-temperature continuous flow synthesis of 1,3,4-oxadiazoles via N-acylation of 5-substituted tetrazoles Tetrahedron Lett. 53 2012 952 955
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 952-955
-
-
Reichart, B.1
Kappe, C.O.2
-
8
-
-
80955129995
-
Cu(II) catalyzed imine C-H functionalization leading to synthesis of 2,5-substituted 1,3,4-oxadiazoles
-
S. Guin, T. Ghosh, S.K. Rout, A. Banerjee, and B.K. Patel Cu(II) catalyzed imine C-H functionalization leading to synthesis of 2,5-substituted 1,3,4-oxadiazoles Org. Lett. 13 2011 5976 5979
-
(2011)
Org. Lett.
, vol.13
, pp. 5976-5979
-
-
Guin, S.1
Ghosh, T.2
Rout, S.K.3
Banerjee, A.4
Patel, B.K.5
-
9
-
-
33746802369
-
One pot direct synthesis of oxazolines, benzoxazoles, and oxadiazoles from carboxylic acids using the deoxo-fluor reagent
-
C.O. Kangani, D.E. Kelley, and B.W. Day One pot direct synthesis of oxazolines, benzoxazoles, and oxadiazoles from carboxylic acids using the deoxo-fluor reagent Tetrahedron Lett. 47 2006 6497 6499
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 6497-6499
-
-
Kangani, C.O.1
Kelley, D.E.2
Day, B.W.3
-
10
-
-
77951085083
-
Polyethylene glycol (PEG) mediated green synthesis of 2,5-disubstituted 1,3,4-oxadiazoles catalyzed by ceric ammonium nitrate (CAN)
-
M. Kidwai, D. Bhatnagar, and N.K. Mishra Polyethylene glycol (PEG) mediated green synthesis of 2,5-disubstituted 1,3,4-oxadiazoles catalyzed by ceric ammonium nitrate (CAN) Green Chem. Lett. Rev. 3 2010 55 59
-
(2010)
Green Chem. Lett. Rev.
, vol.3
, pp. 55-59
-
-
Kidwai, M.1
Bhatnagar, D.2
Mishra, N.K.3
-
11
-
-
0035024669
-
Rapid synthesis of 2,5-disubstituted 1,3,4-oxadiazoles under microwave irradiation
-
F. Bentiss, M. Lagrenée, and D. Barbry Rapid synthesis of 2,5-disubstituted 1,3,4-oxadiazoles under microwave irradiation Syn. Commun. 31 2001 935 938
-
(2001)
Syn. Commun.
, vol.31
, pp. 935-938
-
-
Bentiss, F.1
Lagrenée, M.2
Barbry, D.3
-
12
-
-
0043065473
-
An expeditious and convenient one pot synthesis of 2,5-disubstituted 1,3,4-oxadiazoles
-
S.H. Mashraqui, S.G. Ghadigaonkarm, and R.S. Kenny An expeditious and convenient one pot synthesis of 2,5-disubstituted 1,3,4-oxadiazoles Syn. Commun. 33 2003 2541 2545
-
(2003)
Syn. Commun.
, vol.33
, pp. 2541-2545
-
-
Mashraqui, S.H.1
Ghadigaonkarm, S.G.2
Kenny, R.S.3
-
13
-
-
84862197474
-
3 as the nitrogen source, mediated by tin microspheres in aqueous medium
-
3 as the nitrogen source, mediated by tin microspheres in aqueous medium Chem. Commun. 48 2012 6574 6576
-
(2012)
Chem. Commun.
, vol.48
, pp. 6574-6576
-
-
Zhang, L.1
Chen, H.2
Zha, Z.G.3
Wang, Z.Y.4
-
14
-
-
79955148862
-
Direct electrochemical imidation of aliphatic amines via anodic oxidation
-
L. Zhang, J.H. Su, and S.J. Wang Direct electrochemical imidation of aliphatic amines via anodic oxidation Chem. Commun. 47 2011 5488 5490
-
(2011)
Chem. Commun.
, vol.47
, pp. 5488-5490
-
-
Zhang, L.1
Su, J.H.2
Wang, S.J.3
-
15
-
-
77956811821
-
An electrochemical tandem reaction: One-pot synthesis of homoallylic alcohols from alcohols in aqueous media
-
L. Zhang, Z.G. Zha, Z.L. Zhang, Y.F. Li, and Z.Y. Wang An electrochemical tandem reaction: one-pot synthesis of homoallylic alcohols from alcohols in aqueous media Chem. Commun. 46 2010 7196 7198
-
(2010)
Chem. Commun.
, vol.46
, pp. 7196-7198
-
-
Zhang, L.1
Zha, Z.G.2
Zhang, Z.L.3
Li, Y.F.4
Wang, Z.Y.5
-
20
-
-
84870007967
-
Tetrabutylammonium iodide catalyzed allylic sulfonylation of α-methyl styrene derivatives with sulfonylhydrazides
-
X.Q. Li, X.S. Xu, and C. Zhou Tetrabutylammonium iodide catalyzed allylic sulfonylation of α-methyl styrene derivatives with sulfonylhydrazides Chem. Commun. 48 2012 12240 12250
-
(2012)
Chem. Commun.
, vol.48
, pp. 12240-12250
-
-
Li, X.Q.1
Xu, X.S.2
Zhou, C.3
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