-
1
-
-
7044235263
-
Domino reactions in organic synthesis
-
doi:10.1021/cr950027e
-
Lutzf T (1996) Domino reactions in organic synthesis. Chem Rev 96:115-136. doi:10.1021/cr950027e
-
(1996)
Chem Rev
, vol.96
, pp. 115-136
-
-
Lutzf, T.1
-
2
-
-
31544434530
-
Recent developments in isocyanide based multicomponent reactions in applied chemistry
-
doi:10.1021/cr0505728
-
Dömling A (2006) Recent developments in isocyanide based multicomponent reactions in applied chemistry. Chem Rev 106:17-89. doi:10.1021/cr0505728
-
(2006)
Chem Rev
, vol.106
, pp. 17-89
-
-
Dömling, A.1
-
3
-
-
17144366282
-
Asymmetric multicomponent reactions (AMCRs): The new frontier
-
doi:10.1002/anie.200460548
-
Ramón DJ, Yus M (2005) Asymmetric multicomponent reactions (AMCRs): the new frontier. Angew Chem Int Ed 44:1602-1634. doi:10.1002/anie. 200460548
-
(2005)
Angew Chem Int Ed
, vol.44
, pp. 1602-1634
-
-
Ramón, D.J.1
Yus, M.2
-
4
-
-
2542509173
-
Multicomponent reactions with isocyanides
-
doi:10.1002/1521-3773(20000915)
-
Dömling A, Ugi I (2000) Multicomponent reactions with isocyanides. Angew Chem Int Ed 39:3168-3210. doi:10.1002/1521-3773(20000915)
-
(2000)
Angew Chem Int Ed
, vol.39
, pp. 3168-3210
-
-
Dömling, A.1
Ugi, I.2
-
5
-
-
0012988147
-
1.4-Dipolare Cycloadditionen, II. Dreikomponenten-Reaktionen des Isochinolins mit Acetylendicarbonsäureester und verschiedenen Dipolarophilen
-
doi:10.1002/cber.19671000406
-
Huisgen R, Morikawa M, Herbig K, Brunn E (1967) 1.4-Dipolare Cycloadditionen, II. Dreikomponenten-Reaktionen des Isochinolins mit Acetylendicarbonsäureester und verschiedenen Dipolarophilen. Chem Ber 100:1094-1106. doi:10.1002/cber.19671000406
-
(1967)
Chem Ber
, vol.100
, pp. 1094-1106
-
-
Huisgen, R.1
Morikawa, M.2
Herbig, K.3
Brunn, E.4
-
6
-
-
0348147693
-
Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes
-
doi:10.1021/ar020258p
-
Nair V, Rajesh C, Vinod AU, Bindu S, Sreekanth AR, Mathen JS, Balagopal L (2003) Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes. Acc Chem Res 36:899-907. doi:10.1021/ar020258p
-
(2003)
Acc Chem Res
, vol.36
, pp. 899-907
-
-
Nair, V.1
Rajesh, C.2
Vinod, A.U.3
Bindu, S.4
Sreekanth, A.R.5
Mathen, J.S.6
Balagopal, L.7
-
7
-
-
33748357553
-
Engaging zwitterions in carbon-carbon and carbon-nitrogen bondforming reactions: A promising synthetic strategy
-
doi:10.1021/ar0502026
-
Nair V, Menon RS, Sreekanth A, Abhilash N, Biju AT (2006) Engaging zwitterions in carbon-carbon and carbon-nitrogen bondforming reactions: a promising synthetic strategy. Acc Chem Res 39:520-530. doi:10.1021/ar0502026
-
(2006)
Acc Chem Res
, vol.39
, pp. 520-530
-
-
Nair, V.1
Menon, R.S.2
Sreekanth, A.3
Abhilash, N.4
Biju, A.T.5
-
8
-
-
81855187571
-
Recent developments in reissert-type multicomponent reactions
-
doi:10.1007/7081-2010-42
-
Kielland N, Lavilla R (2010) Recent developments in reissert-type multicomponent reactions. Top Heterocycl Chem 25:127-168. doi:10.1007/7081-2010- 42
-
(2010)
Top Heterocycl Chem
, vol.25
, pp. 127-168
-
-
Kielland, N.1
Lavilla, R.2
-
9
-
-
79953294313
-
Recent progress of isocyanide-based multicomponent reactions in Iran
-
doi:10.1007/s11030-010-9258-1
-
Shaabani A, Rezayan AH, Sarvary A (2011) Recent progress of isocyanide-based multicomponent reactions in Iran. Mol Divers 15:41-68. doi:10.1007/s11030-010-9258-1
-
(2011)
Mol Divers
, vol.15
, pp. 41-68
-
-
Shaabani, A.1
Rezayan, A.H.2
Sarvary, A.3
-
10
-
-
40049108767
-
Construction of heterocycles via 1,4-dipolar cycloaddition of quinoline- DMAD zwitterion with various dipolarophiles
-
doi:10.1016/j.tet.2008.01.106
-
Nair V, Devipriya S, Suresh E (2008) Construction of heterocycles via 1,4-dipolar cycloaddition of quinoline- DMAD zwitterion with various dipolarophiles. Tetrahedron 64:3567-3577. doi:10.1016/j.tet.2008.01.106
-
(2008)
Tetrahedron
, vol.64
, pp. 3567-3577
-
-
Nair, V.1
Devipriya, S.2
Suresh, E.3
-
11
-
-
34247196011
-
Efficient synthesis of [1,3]oxazino[2,3-a]quinoline derivatives by a novel 1,4-dipolar cycloaddition involving a quinoline-DMAD zwitterion and carbonyl compounds
-
DOI 10.1016/j.tetlet.2007.03.123, PII S0040403907005928
-
Nair V, Devipriya S, Suresh E (2007) Efficient synthesis of [1,3]oxazino[2,3-a]quinoline derivatives by a novel 1,4-dipolar cycloaddition involving a quinoline-DMAD zwitterion and carbonyl compounds. Tetrahedron Lett 48:3667-3670. doi:10.1016/j.tetlet.2007.03.123 (Pubitemid 46627824)
-
(2007)
Tetrahedron Letters
, vol.48
, Issue.21
, pp. 3667-3670
-
-
Nair, V.1
Devipriya, S.2
Eringathodi, S.3
-
12
-
-
33645018061
-
Reaction of dimethoxycarbene-DMAD zwitterion with 1,2-diones and anhydrides: A novel synthesis of highly substituted dihydrofurans and spirodihydrofurans
-
doi:10.1021/jo052429k
-
Nair V, Deepthi A, Manoj P, Bindu S, Sreekumar V, Beneesh PB, Mohan R, Suresh E (2006) Reaction of dimethoxycarbene-DMAD zwitterion with 1,2-diones and anhydrides: a novel synthesis of highly substituted dihydrofurans and spirodihydrofurans. J Org Chem 71:2313-2319. doi:10.1021/jo052429k
-
(2006)
J Org Chem
, vol.71
, pp. 2313-2319
-
-
Nair, V.1
Deepthi, A.2
Manoj, P.3
Bindu, S.4
Sreekumar, V.5
Beneesh, P.B.6
Mohan, R.7
Suresh, E.8
-
13
-
-
20544467959
-
Two unprecedented multicomponent reactions involving N-heterocyclic carbenes, activated acetylenes, and aldehydes
-
DOI 10.1021/ol0502782
-
Nair V, Sreekumar V, Bindu S, Suresh E (2005) Two unprecedented multicomponent reactions involving N-heterocyclic carbenes, activated acetylenes, and aldehydes. Org Lett 70:2297-2300. doi:10.1021/ol0502782 (Pubitemid 40847621)
-
(2005)
Organic Letters
, vol.7
, Issue.12
, pp. 2297-2300
-
-
Nair, V.1
Sreekumar, V.2
Bindu, S.3
Suresh, E.4
-
14
-
-
71149083346
-
Diastereoselective synthesis of spiro-functionalized tetraalkyl benzoisoquinopyrrolonaphthyridine-tetracarboxylates from isoquinoline, dialkyl acetylenedicarboxylates, and indane-1,3-dione
-
doi:10.1016/j.tetlet.2009.11.040
-
Yavari I, Mirzaei A, Moradi L, Khalili G (2010) Diastereoselective synthesis of spiro-functionalized tetraalkyl benzoisoquinopyrrolonaphthyridine- tetracarboxylates from isoquinoline, dialkyl acetylenedicarboxylates, and indane-1,3-dione. Tetrahedron Lett 51:396-398. doi:10.1016/j.tetlet.2009.11.040
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 396-398
-
-
Yavari, I.1
Mirzaei, A.2
Moradi, L.3
Khalili, G.4
-
15
-
-
77949487520
-
Formation of trialkyl quinoline- 2,3,4-tricarboxylates by reaction of isatin, dialkyl acetylenedicarboxylates, and sodium O -alkyl carbonodithioates
-
doi:10.1016/j.tetlet.2010.02.107
-
Yavari I, Seyfi S, Hossaini Z (2010) Formation of trialkyl quinoline- 2,3,4-tricarboxylates by reaction of isatin, dialkyl acetylenedicarboxylates, and sodium O -alkyl carbonodithioates.Tetrahedron Lett 51:2193-2194. doi:10.1016/j.tetlet.2010.02.107
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 2193-2194
-
-
Yavari, I.1
Seyfi, S.2
Hossaini, Z.3
-
16
-
-
59449108816
-
Synthesis of pyrrolo[2,1-a]isoquinolines from activated acetylenes, benzoylnitromethanes, and isoquinoline
-
doi:10.1016/j.tet.2009.01.001
-
Yavari I, Piltan M, Moradi L (2009) Synthesis of pyrrolo[2,1-a] isoquinolines from activated acetylenes, benzoylnitromethanes, and isoquinoline. Tetrahedron 65:2067-2071. doi:10.1016/j.tet.2009.01.001
-
(2009)
Tetrahedron
, vol.65
, pp. 2067-2071
-
-
Yavari, I.1
Piltan, M.2
Moradi, L.3
-
17
-
-
42749088760
-
Reaction of benzoyl chlorides with Huisgen's zwitterion: Synthesis of functionalized 2,5-dihydro-1H-pyrroles and tetrasubstituted
-
doi:10.1016/j.tet.2008.03.044
-
Yavari I, Mokhtarporyani-Sanandaj A, Moradi L, Mirzaei A (2008) Reaction of benzoyl chlorides with Huisgen's zwitterion: synthesis of functionalized 2,5-dihydro-1H-pyrroles and tetrasubstituted. Tetrahedron 64:5221-5225. doi:10.1016/j.tet.2008.03.044
-
(2008)
Tetrahedron
, vol.64
, pp. 5221-5225
-
-
Yavari, I.1
Mokhtarporyani-Sanandaj, A.2
Moradi, L.3
Mirzaei, A.4
-
18
-
-
51549094557
-
Gold(III) chloride-catalyzed three-component reaction: A facile synthesis of alkynyl derivatives of 1,2-dihydroquinolines and isoquinolines
-
doi:10.1021/jo8007034
-
Yadav JS, Reddy BVS, Yadav NN, Gupta MK, Sridhar B (2008) Gold(III) chloride-catalyzed three-component reaction: a facile synthesis of alkynyl derivatives of 1,2-dihydroquinolines and isoquinolines. J Org Chem 73:6857-6859. doi:10.1021/jo8007034
-
(2008)
J Org Chem
, vol.73
, pp. 6857-6859
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Yadav, N.N.3
Gupta, M.K.4
Sridhar, B.5
-
19
-
-
40949165028
-
Concise assembly of highly substituted furan-fused 1,4-thiazepines and their Diels-Alder reactions with benzynes
-
DOI 10.1021/jo702299m
-
Ding HF, Zhang YP, Bian M, Yao WJ, Ma C (2008) Concise assembly of highly substituted furan-fused 1,4-thiazepines and their Diels-Alder reactions with benzynes. J Org Chem 73:578-584. doi:10.1021/jo702299m (Pubitemid 351437418)
-
(2008)
Journal of Organic Chemistry
, vol.73
, Issue.2
, pp. 578-584
-
-
Ding, H.1
Zhang, Y.2
Bian, M.3
Yao, W.4
Ma, C.5
-
20
-
-
33749131944
-
Synthesis of new 2-vinylation products of indole via a Michael-type addition reaction with dimethyl acetylenedicarboxylate and their Diels-Alder reactivity as precursors of new carbazoles
-
doi:10.1021/jo061336f
-
Çavdar H, Saraçoglu N (2006) Synthesis of new 2-vinylation products of indole via a Michael-type addition reaction with dimethyl acetylenedicarboxylate and their Diels-Alder reactivity as precursors of new carbazoles. J Org Chem 71:7793-7799. doi:10.1021/jo061336f
-
(2006)
J Org Chem
, vol.71
, pp. 7793-7799
-
-
Çavdar, H.1
Saraçoglu, N.2
-
21
-
-
4043076180
-
Multicomponent reactions of diazoamides: Diastereoselective synthesis of mono- and bis-spirofurooxindoles
-
DOI 10.1021/jo0493119
-
Muthusamy S, Gunanathan C, Nethaji M (2004) Multicomponent reactions of diazoamides: diastereoselective synthesis of monoand bis-spirofurooxindoles. J Org Chem 69:5631-5637. doi:10.1021/jo0493119 (Pubitemid 39079617)
-
(2004)
Journal of Organic Chemistry
, vol.69
, Issue.17
, pp. 5631-5637
-
-
Muthusamy, S.1
Gunanathan, C.2
Nethaji, M.3
-
22
-
-
77953122616
-
[2+2] Cycloaddition of electronpoor acetylenes to (E) -3-dimethylamino-1-heteroaryl-prop-2-en-1-ones: Synthesis of highly functionalized 1-heteroaroyl-1,3-butadienes
-
doi:10.1016/j.tetlet.2010.04.106
-
Bezenšek J, Koleša T, Grošelj U, Wagger J, Stare K, Meden A, Svete J, Stanovnik B (2010) [2+2] Cycloaddition of electronpoor acetylenes to (E) -3-dimethylamino-1-heteroaryl-prop-2-en-1-ones: synthesis of highly functionalized 1-heteroaroyl-1,3-butadienes. Tetrahedron Lett 51:3392-3397. doi:10.1016/j.tetlet.2010.04.106
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 3392-3397
-
-
Bezenšek, J.1
Koleša, T.2
Grošelj, U.3
Wagger, J.4
Stare, K.5
Meden, A.6
Svete, J.7
Stanovnik, B.8
-
23
-
-
70349780557
-
A simple and convenient synthesis of 2-(perfluoroalkyl)-4H -chromenes from salicyl N -tosylimines or salicylaldehydes and methyl 2-perfluoroalkynoates
-
doi:10.1016/j.tet.2009.09.030
-
Lu L, Wei JM, Chen J, Zhang JP, Deng HM, Shao M, Zhang H, Cao WG (2009) A simple and convenient synthesis of 2-(perfluoroalkyl)-4H -chromenes from salicyl N -tosylimines or salicylaldehydes and methyl 2-perfluoroalkynoates. Tetrahedron 65:9152-9156. doi:10.1016/j.tet.2009.09.030
-
(2009)
Tetrahedron
, vol.65
, pp. 9152-9156
-
-
Lu, L.1
Wei, J.M.2
Chen, J.3
Zhang, J.P.4
Deng, H.M.5
Shao, M.6
Zhang, H.7
Cao, W.G.8
-
24
-
-
60349129901
-
A simple and effective approach to the synthesis of rhodanine derivatives via three-component reactions in water
-
doi:10.1016/j.tetlet.2008.12.107
-
Alizadeh A, Rostamnia S, Hosseinpour N (2009) A simple and effective approach to the synthesis of rhodanine derivatives via three-component reactions in water. Tetrahedron Lett 50:1533-1535. doi:10.1016/j.tetlet.2008.12.107
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 1533-1535
-
-
Alizadeh, A.1
Rostamnia, S.2
Hosseinpour, N.3
-
25
-
-
84867356066
-
A domino synthetic strategy leading to two-carbon-tethered fused acridine/indole pairs and fused acridine derivatives
-
doi:10.1039/C2OB26315G
-
Jiang B, Wang X, Li MY, Wu Q, Ye Q, Xu HW, Tu SJ (2012) A domino synthetic strategy leading to two-carbon-tethered fused acridine/indole pairs and fused acridine derivatives. Org Biomol Chem 10:8533-8538. doi:10.1039/C2OB26315G
-
(2012)
Org Biomol Chem
, vol.10
, pp. 8533-8538
-
-
Jiang, B.1
Wang, X.2
Li, M.Y.3
Wu, Q.4
Ye, Q.5
Xu, H.W.6
Tu, S.J.7
-
26
-
-
77955680733
-
Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate
-
doi:10.1021/ol101475b
-
Sun J, Xia EY, Wu Q, Yan CG (2010) Synthesis of polysubstituted dihydropyridines by four-component reactions of aromatic aldehydes, malononitrile, arylamines, and acetylenedicarboxylate. Org Lett 12:3678-3681. doi:10.1021/ol101475b
-
(2010)
Org Lett
, vol.12
, pp. 3678-3681
-
-
Sun, J.1
Xia, E.Y.2
Wu, Q.3
Yan, C.G.4
-
27
-
-
79960203842
-
Synthesis of 3,4-dihydropyridin-2(1H)-ones and 3,4-dihydro-2H-pyrans via fourcomponent reactions of aromatic aldehydes, cyclic 1,3-carbonyls, arylamines, and dimethyl acetylenedicarboxylate
-
doi:10.1021/co200045t
-
Sun J, Xia EY, Wu Q, Yan CG (2011) Synthesis of 3,4-dihydropyridin-2(1H)- ones and 3,4-dihydro-2H-pyrans via fourcomponent reactions of aromatic aldehydes, cyclic 1,3-carbonyls, arylamines, and dimethyl acetylenedicarboxylate. ACS Comb Sci 13:421-426. doi:10.1021/co200045t
-
(2011)
ACS Comb Sci
, vol.13
, pp. 421-426
-
-
Sun, J.1
Xia, E.Y.2
Wu, Q.3
Yan, C.G.4
-
28
-
-
79956371243
-
Molecular diversity of three-component reactions of aromatic aldehydes, arylamines, and acetylenedicarboxylates
-
doi:10.1002/ejoc.201100008
-
Sun J, Wu Q, Xia EY, Yan CG (2011) Molecular diversity of three-component reactions of aromatic aldehydes, arylamines, and acetylenedicarboxylates. Eur J Org Chem 16:2981-2986. doi:10.1002/ejoc.201100008
-
(2011)
Eur J Org Chem
, vol.16
, pp. 2981-2986
-
-
Sun, J.1
Wu, Q.2
Xia, E.Y.3
Yan, C.G.4
-
29
-
-
79960248404
-
Synthesis of functionalized 2-aminohydropyridines and 2-pyridinones via domino reactions of arylamines,methyl propiolate, aromatic aldehydes, and substituted acetonitriles
-
doi:10.1021/co200071v
-
Sun J, Sun Y, Xia EY, Yan CG (2011) Synthesis of functionalized 2-aminohydropyridines and 2-pyridinones via domino reactions of arylamines,methyl propiolate, aromatic aldehydes, and substituted acetonitriles. ACS Comb Sci 13:436-441. doi:10.1021/co200071v
-
(2011)
ACS Comb Sci
, vol.13
, pp. 436-441
-
-
Sun, J.1
Sun, Y.2
Xia, E.Y.3
Yan, C.G.4
-
30
-
-
84867704834
-
Facile synthesis of dispirooxindole-fused heterocycles via domino 1,4-dipolar addition and Diels-Alder reaction of in situ generated Huisgen 1,4-dipoles
-
doi:10.1021/ol302530m
-
Sun J, Sun Y, Gong H, Xie YJ, Yan CG (2012) Facile synthesis of dispirooxindole-fused heterocycles via domino 1,4-dipolar addition and Diels-Alder reaction of in situ generated Huisgen 1,4-dipoles. Org Lett 14:5172-5175. doi:10.1021/ol302530m
-
(2012)
Org Lett
, vol.14
, pp. 5172-5175
-
-
Sun, J.1
Sun, Y.2
Gong, H.3
Xie, Y.J.4
Yan, C.G.5
-
31
-
-
84865075703
-
Efficient synthesis of pentasubstituted pyrroles via one-pot reactions of arylamines, acetylenedicarboxylates and 3-phenacylideneoxindoles
-
doi:10.1016/j.tet.2012.07.056
-
Han Y, Sun Y, Sun J, Yan CG (2012) Efficient synthesis of pentasubstituted pyrroles via one-pot reactions of arylamines, acetylenedicarboxylates and 3-phenacylideneoxindoles. Tetrahedron 68:8256-8260. doi:10.1016/j.tet.2012.07.056
-
(2012)
Tetrahedron
, vol.68
, pp. 8256-8260
-
-
Han, Y.1
Sun, Y.2
Sun, J.3
Yan, C.G.4
-
32
-
-
84865599433
-
Synthesis of the functionalized spiro[indoline-3,5′-pyrroline]-2, 2′-diones via threecomponent reactions of arylamines, acetylenedicarboxylates, and isatins
-
doi:10.1016/j.tet.2012.08.030
-
Han Y, Wu Q, Sun J, Yan CG (2012) Synthesis of the functionalized spiro[indoline-3,5′-pyrroline]-2,2′-diones via threecomponent reactions of arylamines, acetylenedicarboxylates, and isatins. Tetrahedron 68:8539-8544. doi:10.1016/j.tet.2012.08.030
-
(2012)
Tetrahedron
, vol.68
, pp. 8539-8544
-
-
Han, Y.1
Wu, Q.2
Sun, J.3
Yan, C.G.4
-
33
-
-
84863376914
-
Synthesis of spiro[indoline-3,2′-quinoline] derivatives through a four-component reaction
-
doi:10.1002/ejoc.201101737
-
Sun J, Sun Y, Gao H, Yan CG (2012) Synthesis of spiro[indoline-3, 2′-quinoline] derivatives through a four-component reaction. Eur J Org Chem 10:1976-1983. doi:10.1002/ejoc.201101737
-
(2012)
Eur J Org Chem
, vol.10
, pp. 1976-1983
-
-
Sun, J.1
Sun, Y.2
Gao, H.3
Yan, C.G.4
-
34
-
-
84876274003
-
Diastereoselective synthesis of arylidene bis(3-arylaminoacrylates) via one-pot domino reactions
-
doi:10.1002/cjoc.201300094
-
Liu ZM, Zhang LL, Sun J, Yan CG (2013) Diastereoselective synthesis of arylidene bis(3-arylaminoacrylates) via one-pot domino reactions. Chin J Chem 31:479-484. doi:10.1002/cjoc.201300094
-
(2013)
Chin J Chem
, vol.31
, pp. 479-484
-
-
Liu, Z.M.1
Zhang, L.L.2
Sun, J.3
Yan, C.G.4
-
35
-
-
74949114488
-
One-pot silver-catalyzed and PIDA-mediated sequential reactions: Synthesis of polysubstituted pyrroles directly from alkynoates and amines
-
doi:10.1021/ol9026478
-
Liu WB, Jiang HF, Huang LB (2010) One-pot silver-catalyzed and PIDA-mediated sequential reactions: synthesis of polysubstituted pyrroles directly from alkynoates and amines. Org Lett 12:312-315. doi:10.1021/ol9026478
-
(2010)
Org Lett
, vol.12
, pp. 312-315
-
-
Liu, W.B.1
Jiang, H.F.2
Huang, L.B.3
-
36
-
-
77954986510
-
Acid-catalyzed cascade reactions of enaminones with aldehydes: C-H functionalization to afford 1,4-dihydropyridines
-
doi:10.1002/ejoc.201000607
-
Yang JY, Wang CY, Xie X, Li HF, Li YZ (2010) Acid-catalyzed cascade reactions of enaminones with aldehydes: C-H functionalization to afford 1,4-dihydropyridines. Eur J Org Chem 22:4189-4193. doi:10.1002/ejoc.201000607
-
(2010)
Eur J Org Chem
, vol.22
, pp. 4189-4193
-
-
Yang, J.Y.1
Wang, C.Y.2
Xie, X.3
Li, H.F.4
Li, Y.Z.5
-
37
-
-
77954349755
-
Novel synthetic route to 1,4-dihydropyridines from β-amino acrylates by using titanium(IV) chloride under facile conditions
-
doi:10.1016/j.tet.2010.04.102
-
Sirijindalert T, Hansuthirakul K, Rashatasakhon P, Sukwattanasinitt M, Ajavakom A (2010) Novel synthetic route to 1,4-dihydropyridines from β-amino acrylates by using titanium(IV) chloride under facile conditions. Tetrahedron 66:5161-5167. doi:10.1016/j.tet.2010.04.102
-
(2010)
Tetrahedron
, vol.66
, pp. 5161-5167
-
-
Sirijindalert, T.1
Hansuthirakul, K.2
Rashatasakhon, P.3
Sukwattanasinitt, M.4
Ajavakom, A.5
-
38
-
-
36549090410
-
Catalytic synthesis of 1,4-dihydropyridine derivatives using scandium(III) triflate
-
DOI 10.1016/j.tetlet.2007.11.003, PII S004040390702179X
-
Kikuchi S, Iwai M, Murayama H, Fukuzawa S (2008) Catalytic synthesis of 1,4-dihydropyridine derivatives using scandium(III) triflate. Tetrahedron Lett 49:114-116. doi:10.1016/j.tet.2007.11.003 (Pubitemid 350191875)
-
(2008)
Tetrahedron Letters
, vol.49
, Issue.1
, pp. 114-116
-
-
Kikuchi, S.1
Iwai, M.2
Murayama, H.3
Fukuzawa, S.-i.4
|