-
2
-
-
80051966186
-
New approach to the multicomponent one pot synthesis of 2-aryl-1 H -phenanthro[9,10- d ] imidazoles
-
Damavandi, S. New approach to the multicomponent one pot synthesis of 2-aryl-1 H -phenanthro[9,10- d ] imidazoles. Heterocycl. Commun . 2011 , 17 , 79-81.
-
(2011)
Heterocycl. Commun .
, vol.17
, pp. 79-81
-
-
Damavandi, S.1
-
4
-
-
77955023777
-
2 O-catalyzed, three-component, one-potsynthesis of indeno[1,2-b]quinoline-7-one derivatives
-
2 O-catalyzed, three-component, one-potsynthesis of indeno[1,2-b]quinoline-7-one derivatives. Synth. Commun . 2010 , 40 , 2402-2406.
-
(2010)
Synth. Commun .
, vol.40
, pp. 2402-2406
-
-
Heravi, M.M.1
Hosseini, T.2
Derikvand, F.3
Beheshtiha, S.4
Bamoharram, F.5
-
5
-
-
0031001699
-
Solid-phase organic reactions II: A review of the literature Nov 95-Nov 96
-
DOI 10.1016/S0040-4020(97)00279-2, PII S0040402097002792
-
Hermakens, P. H. H.; Ottenheijm, H. C. J.; Rees, D. C. Solid-phase organic reactions II: a review of the literature Nov 95 - Nov 96. Tetrahedron 1997 , 53 , 5643-5678. (Pubitemid 27166277)
-
(1997)
Tetrahedron
, vol.53
, Issue.16
, pp. 5643-5678
-
-
Hermkens, P.H.H.1
Ottenheijm, H.C.J.2
Rees, D.C.3
-
6
-
-
0037184893
-
Zn(II)-mediated alkynylation - Cyclization of o-trifl uoroacetyl anilines: One-pot synthesis of 4-trifl uoromethyl- substituted quinoline derivatives
-
Jiang, B.; Si, Y. C. Zn(II)-mediated alkynylation - cyclization of o-trifl uoroacetyl anilines: one-pot synthesis of 4-trifl uoromethyl- substituted quinoline derivatives. J. Org. Chem. 2002 , 67 , 9449-9453.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 9449-9453
-
-
Jiang, B.1
Si, Y.C.2
-
7
-
-
34250021382
-
The domino way to heterocycles
-
DOI 10.1016/j.tet.2007.03.158, PII S0040402007006126
-
Padwa, A.; Bur, S. K. The domino way to heterocycles. Tetrahedron 2007 , 63 , 5341-5378. (Pubitemid 46881030)
-
(2007)
Tetrahedron
, vol.63
, Issue.25
, pp. 5341-5378
-
-
Padwa, A.1
Bur, S.K.2
-
9
-
-
0037140878
-
Novel facile synthesis of 2,2,4 substituted 1,2-dihydroquinolines via a modified Skraup reaction
-
DOI 10.1016/S0040-4039(02)00614-7, PII S0040403902006147
-
Theoclitou, M. E.; Robinson, L. A. Novel facile synthesis of 2,2,4- substituted 1,2-dihydroquinolines via a modifi ed Skraup reaction. Tetrahedron Lett . 2002 , 43 , 3907-3910. (Pubitemid 34463060)
-
(2002)
Tetrahedron Letters
, vol.43
, Issue.21
, pp. 3907-3910
-
-
Theoclitou, M.-E.1
Robinson, L.A.2
-
10
-
-
33750309194
-
Atom economy - A challenge for organic synthesis: Homogeneous catalysis leads the way
-
Trost, B. M. Atom economy - A challenge for organic synthesis: homogeneous catalysis leads the way. Angew. Chem. Int. Ed. Engl. 1995 , 34 , 259-281.
-
(1995)
Angew. Chem. Int. Ed. Engl.
, vol.34
, pp. 259-281
-
-
Trost, B.M.1
-
11
-
-
33748968361
-
An effi cient one-pot, three-component synthesis of indeno[1,2-b] quinoline-9,11(6H,10H)-dione,acridine-1,8(2H,5H)-dione, and quinoline-3- carbonitrile derivatives from enaminones
-
Tu, S. J.; Jiang, B.; Jia, R. H.; Zhang, J. Y.; Zhang, Y.; Yao, C. S.; Shi, F. An effi cient one-pot, three-component synthesis of indeno[1,2-b] quinoline-9,11(6H,10H)-dione, acridine-1,8(2H,5H)-dione, and quinoline-3-carbonitrile derivatives from enaminones. Org. Biomol. Chem . 2006a , 4 , 3664-3673.
-
(2006)
Org. Biomol. Chem .
, vol.4
, pp. 3664-3673
-
-
Tu, S.J.1
Jiang, B.2
Jia, R.H.3
Zhang, J.Y.4
Zhang, Y.5
Yao, C.S.6
Shi, F.7
-
12
-
-
33750519864
-
A simple procedure for the synthesis of 4-aza-podophyllotoxin derivatives in water under microwave irradiation conditions
-
DOI 10.1055/s-2006-950279
-
Tu, S.; Zhang, Y.; Zhang, J.; Jiang, B.; Jia, R.; Zhang, J.; Ji, S. A simple procedure for the synthesis of 4-aza-podophyllotoxin derivatives in water under microwave irradiation conditions. Synlett 2006b , 17 , 2785-2790. (Pubitemid 44663579)
-
(2006)
Synlett
, Issue.17
, pp. 2785-2790
-
-
Tu, S.1
Zhang, Y.2
Zhang, J.3
Jiang, B.4
Jia, R.5
Zhang, J.6
Ji, S.7
-
13
-
-
34247130916
-
4]: Reactions of arylaldehyde, 3-arylamino-5- ,5-dimethylcyclohex-2-enone and active methylene compounds
-
Wang, X. S.; Zhang, M. M.; Jiang, H.; Yao, C. S.; Tu, S. J. Threecomponent green synthesis of N-arylquinoline derivatives in ionic liquid [Bmim̌][BF 4 ]: Reactions of arylaldehyde, 3-arylamino-5- ,5-dimethylcyclohex-2-enone and active methylene compounds. Tetrahedron 2007 , 63 , 4439-4443.
-
(2007)
Tetrahedron
, vol.63
, pp. 4439-4443
-
-
Wang, X.S.1
Zhang, M.M.2
Jiang, H.3
Yao, C.S.4
Tu, S.J.5
-
14
-
-
46649113366
-
An efficient and highly selective method for the synthesis of 3-arylbenzo-quinoline derivatives catalyzed by iodine via three-component reactions
-
DOI 10.1055/s-2008-1067087, F03708SS
-
Wang, X. S.; Li, Q.; Wu, J. R.; Li, Y. L.; Yao, C. S.; Tu, S. J. An efficient and highly selective method for the synthesis of 3-arylbenzoquinoline derivatives catalyzed by iodine via three component reactions. Synthesis 2008 , 12, 1902-1910. (Pubitemid 351934230)
-
(2008)
Synthesis
, Issue.12
, pp. 1902-1910
-
-
Wang, X.-S.1
Li, Q.2
Wu, J.-R.3
Li, Y.-L.4
Yao, C.-S.5
Tu, S.-J.6
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