-
1
-
-
31544434530
-
Recent developments in isocyanide-based multicomponent reactions in applied chemistry
-
(a) Dömling, A. Recent developments in isocyanide-based multicomponent reactions in applied chemistry. Chem. Rev. 2006, 106, 17-89;
-
(2006)
Chem. Rev.
, vol.106
, pp. 17-89
-
-
Dömling, A.1
-
2
-
-
49949152144
-
Isocyanide-based multicomponent reactions in drug discovery
-
(b) Akritopoulou-Zanze, I. Isocyanide-based multicomponent reactions in drug discovery. Curr. Opin. Chem. Biol. 2008, 12, 324-331.
-
(2008)
Curr. Opin. Chem. Biol.
, vol.12
, pp. 324-331
-
-
Akritopoulou-Zanze, I.1
-
3
-
-
59949090727
-
Beyond the Ugi reaction: Less conventional interactions between isocyanides and iminium species
-
El Kaim, L.; Grimaud, L. Beyond the Ugi reaction: Less conventional interactions between isocyanides and iminium species. Tetrahedron 2009, 65, 2153-2171.
-
(2009)
Tetrahedron
, vol.65
, pp. 2153-2171
-
-
El Kaim, L.1
Grimaud, L.2
-
4
-
-
0037391570
-
Recent developments in the isonitrile-based multicomponent synthesis of heterocycles
-
Zhu, J. Recent developments in the isonitrile-based multicomponent synthesis of heterocycles. Eur. J. Org. Chem. 2003, 1133-1144.
-
(2003)
Eur. J. Org. Chem.
, pp. 1133-1144
-
-
Zhu, J.1
-
5
-
-
34247860900
-
Synthesis of 1 2, 3,4-tetrahydroisoquinoline-1-carboxylic acid derivatives via Ugi reactions
-
(a) Schuster, I.; Sztojkov-Ivanov, A.; Lázár, L.; Fülöp, F. Synthesis of 1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid derivatives via Ugi reactions. Lett. Org. Chem. 2007, 4, 102-108;
-
(2007)
Lett. Org. Chem.
, vol.4
, pp. 102-108
-
-
Schuster, I.1
Sztojkov-Ivanov, A.2
Lázár, L.3
Fülöp, F.4
-
6
-
-
34547403674
-
IBX-mediated oxidative Ugi-type multicomponent reactions: Application to the N and C1 functionalization of tetrahydro-isoquinoline
-
(b) Ngouansavanh, T.; Zhu, J. IBX-mediated oxidative Ugi-type multicomponent reactions: Application to the N and C1 functionalization of tetrahydro-isoquinoline. Angew. Chem. Int. Ed. 2007, 46, 5775-5778.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 5775-5778
-
-
Ngouansavanh, T.1
Zhu, J.2
-
7
-
-
34249881653
-
An unexpected, novel, three-component reaction between isoquinoline, an isocyanide, and strong CH-acids in water
-
(a) Shaabani, A.; Soleimani, E.; Khavasi, H. R. An unexpected, novel, three-component reaction between isoquinoline, an isocyanide, and strong CH-acids in water. Tetrahedron Lett. 2007, 48, 4743-4747;
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 4743-4747
-
-
Shaabani, A.1
Soleimani, E.2
Khavasi, H.R.3
-
8
-
-
38349061359
-
A novel three-component reaction for the synthesis of 1,2-dihydroisoquinolines via the reaction of isoquinoline and isocyanides with strong CH-acids in water
-
(b) Shaabani, A.; Soleimani, E.; Moghimi-Rad, J. A novel three-component reaction for the synthesis of 1,2-dihydroisoquinolines via the reaction of isoquinoline and isocyanides with strong CH-acids in water. Tetrahedron Lett. 2008, 49, 1277-1281.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1277-1281
-
-
Shaabani, A.1
Soleimani, E.2
Moghimi-Rad, J.3
-
9
-
-
17744403755
-
N-Acylazinium salts: A new source of iminium ions for Ugi-type processes
-
(a) D́iaz, J. L.; Miguel, M.; Lavilla, R. N-Acylazinium salts: A new source of iminium ions for Ugi-type processes. J. Org. Chem. 2004, 69, 3550-3553;
-
(2004)
J. Org. Chem.
, vol.69
, pp. 3550-3553
-
-
D́iaz, J.L.1
Miguel, M.2
Lavilla, R.3
-
10
-
-
14644439828
-
A three-component synthesis of (1,3-oxazol-2-yl)-1,2-dihydro(iso) quinoline and its further structural diversification
-
(b) Tron, G. C.; Zhu, J. A three-component synthesis of (1,3-oxazol-2-yl)-1,2-dihydro(iso)quinoline and its further structural diversification. Synlett 2005, 532-534.
-
(2005)
Synlett
, pp. 532-534
-
-
Tron, G.C.1
Zhu, J.2
-
11
-
-
0346887176
-
Tetrahydroisoquinoline-based sulfonamide hydroxamates as potent matrix metalloproteinase inhibitors
-
(a) Ma, D.; Wu, W.; Yang, G.; Li, J.; Li, J.; Ye, Q. Tetrahydroisoquinoline-based sulfonamide hydroxamates as potent matrix metalloproteinase inhibitors. Bioorg. Med. Chem. Lett. 2004, 14, 47-50;
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 47-50
-
-
Ma, D.1
Wu, W.2
Yang, G.3
Li, J.4
Li, J.5
Ye, Q.6
-
12
-
-
33847106779
-
Quantitative structure-activity relationship modeling of growth hormone secretago-gues agonist activity of some tetrahydroisoquinoline 1-carboxamides
-
(b) Cabalerro, J.; Zampini, F. M.; Collina, S.; Fernandez, M. Quantitative structure-activity relationship modeling of growth hormone secretago-gues agonist activity of some tetrahydroisoquinoline 1-carboxamides. Chem. Biol. Drug Res. 2007, 69, 48-55;
-
(2007)
Chem. Biol. Drug Res.
, vol.69
, pp. 48-55
-
-
Cabalerro, J.1
Zampini, F.M.2
Collina, S.3
Fernandez, M.4
-
13
-
-
35148871733
-
Enzymatic resolution of methyl (1RS)-N-tBoc-6-hydroxy-3,4-dihydro-1H- isoquinoline-1-carboxylate by Seaprose S
-
(c) Gill, I. S.; Kick, E.; Richlin-Zack, K.; Yang, W.; Wang, Y.; Patel, R. N. Enzymatic resolution of methyl (1RS)-N-tBoc-6-hydroxy-3,4-dihydro-1H- isoquinoline-1-carboxylate by Seaprose S. Tetrahedron: Asymmetry 2007, 18, 2147-2154;
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2147-2154
-
-
Gill, I.S.1
Kick, E.2
Richlin-Zack, K.3
Yang, W.4
Wang, Y.5
Patel, R.N.6
-
14
-
-
55049138054
-
Directed (R)-or (S)-selective dynamic kinetic enzymatic hydrolysis of 1 2, 3,4-tetrahydroisoquinoline-1-carboxylic esters
-
(d) Paal, T. A.; Liljeblad, A.; Kanerva, L. T.; Forro, E.; Fulop, F. Directed (R)-or (S)-selective dynamic kinetic enzymatic hydrolysis of 1,2,3,4-tetrahydroisoquinoline-1-carboxylic esters. Eur. J. Org. Chem. 2008, 5269-5276.
-
(2008)
Eur. J. Org. Chem.
, pp. 5269-5276
-
-
Paal, T.A.1
Liljeblad, A.2
Kanerva, L.T.3
Forro, E.4
Fulop, F.5
-
15
-
-
13444267559
-
Protoberberines from Reissert-compounds, part IX: An alternative approach to dibenzoquinolizine-and isoquinonaphthyridin-13a-carboxylic acids, a novel synthesis of alangimarine
-
Reimann, E.; Grasberger, F. Protoberberines from Reissert-compounds, part IX: An alternative approach to dibenzoquinolizine-and isoquinonaphthyridin-13a- carboxylic acids, a novel synthesis of alangimarine. Monatshefte Chem. 2005, 136, 193-209.
-
(2005)
Monatshefte Chem.
, vol.136
, pp. 193-209
-
-
Reimann, E.1
Grasberger, F.2
-
16
-
-
0001589403
-
Substituted styrenes, VI: Syntheses of the isomeric formylstyrenes and o-and m-vinylbenzoic acid
-
Dale, W. J.; Starr, L.; Strobel, C. W. Substituted styrenes, VI: Syntheses of the isomeric formylstyrenes and o-and m-vinylbenzoic acid. J. Org. Chem. 1961, 26, 2225-2227.
-
(1961)
J. Org. Chem.
, vol.26
, pp. 2225-2227
-
-
Dale, W.J.1
Starr, L.2
Strobel, C.W.3
-
17
-
-
2742567079
-
Synthesis of Ipecacuanha alkaloids 4: Synthesis of ethoxy analog of emetine
-
Rohály, J.; Szántay, C. Synthesis of Ipecacuanha alkaloids, 4: Synthesis of ethoxy analog of emetine. Acta Chim. Acad. Sci. Hung. 1978, 96, 45-54.
-
(1978)
Acta Chim. Acad. Sci. Hung.
, vol.96
, pp. 45-54
-
-
Rohály, J.1
Szántay, C.2
-
18
-
-
0007512008
-
Synthesis of phthalideisoquinolines from 3-halophthalides and 3,4-dihydroisoquinolinium salts
-
Slemon, C. E.; Hellwig, L. C.; Ruder, J.-P.; Hoskins, E. W.; MacLean, D. B. Synthesis of phthalideisoquinolines from 3-halophthalides and 3,4-dihydroisoquinolinium salts. Can. J. Chem. 1981, 59, 3055-3060.
-
(1981)
Can. J. Chem.
, vol.59
, pp. 3055-3060
-
-
Slemon, C.E.1
Hellwig, L.C.2
Ruder, J.-P.3
Hoskins, E.W.4
MacLean, D.B.5
-
19
-
-
33750963335
-
A comparative study of the multicomponent Ugi reactions of an oxabicycloheptene-based b-amino acid in water and in methanol
-
(a) Kanizsai, I.; Szakonyi, Z.; Sillanpää, R.; Fülöp, F. A comparative study of the multicomponent Ugi reactions of an oxabicycloheptene-based b-amino acid in water and in methanol. Tetrahedron Lett. 2006, 47, 9113-9116;
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 9113-9116
-
-
Kanizsai, I.1
Szakonyi, Z.2
Sillanpää, R.3
Fülöp, F.4
-
20
-
-
34047119658
-
Synthesis of bi-and tricyclic b-lactam libraries in aqueous medium
-
(b) Kanizsai, I.; Gyonfalvi, S.; Szakonyi, Z.; Sillanpaa, R.; Fulop, F. Synthesis of bi-and tricyclic b-lactam libraries in aqueous medium. Green Chem. 2007, 9, 357-360.
-
(2007)
Green Chem.
, vol.9
, pp. 357-360
-
-
Kanizsai, I.1
Gyonfalvi, S.2
Szakonyi, Z.3
Sillanpaa, R.4
Fulop, F.5
-
22
-
-
2742528821
-
A convenient synthesis of diastereomeric synthons: Ethyl 3-methyl-1 2, 3,4-tetrahydroisoquinoline-1-acetates by direct and reverse substituent introductions
-
Fülöp, F.; Tari, J.; Bernáth, G.; Sohár, P. A convenient synthesis of diastereomeric synthons: Ethyl 3-methyl-1,2,3,4- tetrahydroisoquinoline-1-acetates by direct and reverse substituent introductions. Heterocycles 1996, 43, 1605-1606.
-
(1996)
Heterocycles
, vol.43
, pp. 1605-1606
-
-
Fülöp, F.1
Tari, J.2
Bernáth, G.3
Sohár, P.4
-
23
-
-
77955043794
-
Oxohexahydropyrazinoisoquinolines
-
Archer, S.; Schulenberg, J. W. Oxohexahydropyrazinoisoquinolines. US Patent 3,798,223, 1974; Chem. Abstr. 1974, 77, 140140.
-
(1974)
US Patent 3 798, 223, 1974, Chem. Abstr
, vol.77
, pp. 140140
-
-
Archer, S.1
Schulenberg, J.W.2
|