-
1
-
-
84937424396
-
Uber die Bildung von Isochinohin-Derivaten durch Einwirkung von methylal auf phenylathylamimi
-
Pictet, A.; Spengler, T. Uber die Bildung von Isochinohin-Derivaten durch Einwirkung von methylal auf phenylathylamimi. Berichte 1911, 44, 2030-2036.
-
(1911)
Berichte
, vol.44
, pp. 2030-2036
-
-
Pictet, A.1
Spengler, T.2
-
2
-
-
4243241249
-
The Pictet-Spengler condensation: A new direction for an old reaction
-
Cox, E. D.; Cook, J. M. The Pictet-Spengler condensation: A new direction for an old reaction. Chem. Rev. 1995, 95, 1797-1842.
-
(1995)
Chem. Rev
, vol.95
, pp. 1797-1842
-
-
Cox, E.D.1
Cook, J.M.2
-
4
-
-
0001373649
-
b-hydroxytryptamine with aldehydes catalyzed by chiral Brønsted acid-assisted Lewis acids
-
b-hydroxytryptamine with aldehydes catalyzed by chiral Brønsted acid-assisted Lewis acids. Synlett 1997, 7, 761-762.
-
(1997)
Synlett
, vol.7
, pp. 761-762
-
-
Kawate, T.1
Yamada, H.2
Matsumizu, M.3
Nishida, A.4
Yamaguchi, K.5
Nakagawa, M.6
-
5
-
-
33748220810
-
Asymmetric Pictet-Spengler reactions employing N,N-phthaloyl amino acids as chiral auxiliary groups
-
Waldmann, H.; Schmidt, G.; Henke, H.; Burkard, M. Asymmetric Pictet-Spengler reactions employing N,N-phthaloyl amino acids as chiral auxiliary groups. Angew. Chem., Int. Ed. Engl. 1995, 34, 2402-2403.
-
(1995)
Angew. Chem., Int. Ed. Engl
, vol.34
, pp. 2402-2403
-
-
Waldmann, H.1
Schmidt, G.2
Henke, H.3
Burkard, M.4
-
6
-
-
0000802968
-
Study of the Pictet-Spengler reaction in aprotic media: Synthesis of the β-galactosidase inhibitor, pyridindolol
-
Soerens, D.; Sandrin, J.; Ungemach, F.; Mokry, P.; Wu, G. S.; Yamanaka, E.; Hutchins, L.; DiPierro, M.; Cook, J. M. Study of the Pictet-Spengler reaction in aprotic media: Synthesis of the β-galactosidase inhibitor, pyridindolol. J. Org. Chem. 1979, 44, 535-545.
-
(1979)
J. Org. Chem
, vol.44
, pp. 535-545
-
-
Soerens, D.1
Sandrin, J.2
Ungemach, F.3
Mokry, P.4
Wu, G.S.5
Yamanaka, E.6
Hutchins, L.7
DiPierro, M.8
Cook, J.M.9
-
7
-
-
5644266177
-
One-step preparation of 1-substituted tetrahydroisoquinolines via the Pictet-Spengler reaction using zeolite catalysts
-
Hegedüs, A.; Hell, Z. One-step preparation of 1-substituted tetrahydroisoquinolines via the Pictet-Spengler reaction using zeolite catalysts. Tetrahedron Lett. 2004, 45, 8553-8555.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 8553-8555
-
-
Hegedüs, A.1
Hell, Z.2
-
8
-
-
11144325118
-
Controlled microwave heating in modern organic synthesis
-
Kappe, C. O. Controlled microwave heating in modern organic synthesis. Angew. Chem., Int. Ed. Engl. 2004, 43, 6250-6284.
-
(2004)
Angew. Chem., Int. Ed. Engl
, vol.43
, pp. 6250-6284
-
-
Kappe, C.O.1
-
9
-
-
0037425327
-
Highly efficient Lewis acid-catalysed Pictet-Spengler reactions discovered by parallel screening
-
Srinivasan, N.; Ganesan, A. Highly efficient Lewis acid-catalysed Pictet-Spengler reactions discovered by parallel screening. Chem. Commun. 2003, 7, 916-917.
-
(2003)
Chem. Commun
, vol.7
, pp. 916-917
-
-
Srinivasan, N.1
Ganesan, A.2
-
10
-
-
0036400027
-
-
Wu, C. Y.; Sun, C. M. Parallel synthesis of 1,2,3,4-tetrahydro-β- carbolines using microwave irradiation. Synlett 2002, 10, 1709-1711.
-
Wu, C. Y.; Sun, C. M. Parallel synthesis of 1,2,3,4-tetrahydro-β- carbolines using microwave irradiation. Synlett 2002, 10, 1709-1711.
-
-
-
-
11
-
-
0037677097
-
Microwave assisted Pictet-Spengler and Bischler-Napieralski reactions
-
Bikash, P.; Parasuraman, J.; Venkatachalam, S. Microwave assisted Pictet-Spengler and Bischler-Napieralski reactions. Synth. Commun. 2003, 33, 2339-2348.
-
(2003)
Synth. Commun
, vol.33
, pp. 2339-2348
-
-
Bikash, P.1
Parasuraman, J.2
Venkatachalam, S.3
-
12
-
-
8544269346
-
A new efficient synthetic methodology for tetrahydroisoquinoline and tetrahydro-β-carboline derivatives using the Pictet-Spengler reaction
-
Campiglia, P.; Gomez-Monterrey, I.; Lama, T.; Novellino, E.; Grieco, P. A new efficient synthetic methodology for tetrahydroisoquinoline and tetrahydro-β-carboline derivatives using the Pictet-Spengler reaction. Molecular Diversity 2004, 8, 427-430.
-
(2004)
Molecular Diversity
, vol.8
, pp. 427-430
-
-
Campiglia, P.1
Gomez-Monterrey, I.2
Lama, T.3
Novellino, E.4
Grieco, P.5
-
13
-
-
0001659860
-
Synthesis of 1-aryl substituted 9H-pyrido[3,4-b]indoles
-
(a) Skinner, W. A.; Parkhurst, R. M. Synthesis of 1-aryl substituted 9H-pyrido[3,4-b]indoles. Can. J. Chem. 1965, 43, 2251-2253;
-
(1965)
Can. J. Chem
, vol.43
, pp. 2251-2253
-
-
Skinner, W.A.1
Parkhurst, R.M.2
-
14
-
-
0035537590
-
-
Agafonov, N. E.; Dudin, A. V.; Preobrazhenskii, A. A.; Zhulin, V. M. Synthesis of 1-aryl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indoles(1,2,3,4- tetrahydro-β-carbolines) under high pressures. Russ. Chem. Bull. 2001, 50, 560-562;
-
(b) Agafonov, N. E.; Dudin, A. V.; Preobrazhenskii, A. A.; Zhulin, V. M. Synthesis of 1-aryl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indoles(1,2,3,4- tetrahydro-β-carbolines) under high pressures. Russ. Chem. Bull. 2001, 50, 560-562;
-
-
-
-
15
-
-
33947338609
-
-
DeGraw, J. I.; Kennedy, J. G.; Skinner, W. A. Substituted 1,2,3,4-tetrahydro-β-carbolines, II. J. Med. Chem. 1967, 10, 127-128.
-
(c) DeGraw, J. I.; Kennedy, J. G.; Skinner, W. A. Substituted 1,2,3,4-tetrahydro-β-carbolines, II. J. Med. Chem. 1967, 10, 127-128.
-
-
-
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