-
1
-
-
0032473509
-
The catalytic enantioselective construction of molecules with quaternary carbon stereocenters
-
Corey, E.J.; Guzman-Perez, A. The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters. Angew. Chem. Int. Ed. 1998, 37, 388-401.
-
(1998)
Angew. Chem. Int. Ed
, vol.37
, pp. 388-401
-
-
Corey, E.J.1
Guzman-Perez, A.2
-
2
-
-
0035905575
-
Enantioselective construction of quaternary stereocenters
-
Christoffers, J.; Mann, A. Enantioselective Construction of Quaternary Stereocenters. Angew. Chem. Int. Ed. 2001, 40, 4591-4597.
-
(2001)
Angew. Chem. Int. Ed
, vol.40
, pp. 4591-4597
-
-
Christoffers, J.1
Mann, A.2
-
3
-
-
37549063959
-
Enantioselective catalytic formation of quaternary stereogenic centers
-
Cozzi, P.G.; Hilgraf, R.; Zimmermann, N. Enantioselective Catalytic Formation of Quaternary Stereogenic Centers. Eur. J. Org. Chem. 2007, 5969-5994.
-
(2007)
Eur. J. Org. Chem
, pp. 5969-5994
-
-
Cozzi, P.G.1
Hilgraf, R.2
Zimmermann, N.3
-
4
-
-
84983433906
-
-
Christoffers, J., Baro, A., Eds.; Wiley-VCH: Weinheim, Germany
-
Christoffers, J.; Baro, A. Quaternary Stereocenters: Challenges and Solution for Organic Synthesis; Christoffers, J., Baro, A., Eds.; Wiley-VCH: Weinheim, Germany, 2005; pp. 83-115.
-
(2005)
Quaternary Stereocenters: Challenges and Solution for Organic Synthesis
, pp. 83-115
-
-
Christoffers, J.1
Baro, A.2
-
5
-
-
67650094837
-
Organocatalytic formation of quaternary stereocenters
-
Bella, M.; Gasperi, T. Organocatalytic Formation of Quaternary Stereocenters. Synthesis 2009, 10, 1583-1614.
-
(2009)
Synthesis
, vol.10
, pp. 1583-1614
-
-
Bella, M.1
Gasperi, T.2
-
6
-
-
84859581400
-
Highly efficient synthesis of n-substituted isoindolinones and phthalazinones using pt nanowires as catalysts
-
Shi, L.; Hu, L.; Wang, J.; Cao, X.; Gu, H. Highly Efficient Synthesis of N-Substituted Isoindolinones and Phthalazinones Using Pt Nanowires as Catalysts. Org. Lett. 2012, 14, 1876-1879.
-
(2012)
Org. Lett
, vol.14
, pp. 1876-1879
-
-
Shi, L.1
Hu, L.2
Wang, J.3
Cao, X.4
Gu, H.5
-
7
-
-
84870184893
-
Active methylene compounds in the synthesis of 3-substituted isobenzofuranones, isoindolinones and related compounds
-
Di Mola, A.; Palombi, L.; Massa, A. Active Methylene Compounds in the Synthesis of 3-substituted Isobenzofuranones, Isoindolinones and Related Compounds. Curr. Org. Chem. 2012, 16, 2302-2320.
-
(2012)
Curr. Org. Chem
, vol.16
, pp. 2302-2320
-
-
Di Mola, A.1
Palombi, L.2
Massa, A.3
-
8
-
-
84983466575
-
-
U.S Patent 2012/0202784 A1, 9 August
-
Aronov, A.; Come, J.H.; Davies, R.J.; Pierce, A.C; Collier, P.N.; Grey, R.L.; O'Dowd, H.; Henderson, J.A.; Krueger, E.B.; Le Tiran, A.; et al. Isoindolinone Inhibitors of Phosphatidylinosytol 3-kinase. U.S. Patent 2012/0202784 A1, 9 August 2012.
-
(2012)
Isoindolinone Inhibitors of Phosphatidylinosytol 3-kinase
-
-
Aronov, A.1
Come, J.H.2
Davies, R.J.3
Pierce, A.C.4
Collier, P.N.5
Grey, R.L.6
O'Dowd, H.7
Henderson, J.A.8
Krueger, E.B.9
Le Tiran, A.10
-
9
-
-
84937820724
-
-
WO2008008022, 17 January
-
Bjoere, A.; Bostroem, J.; Davidsson, O.; Emtenaes, H.; Gran, H.; Iliefski, T.; Kajanus, J.; Olsson, R.; Sandberg, L.; Strandlund, G.; et al. Isoindoline Derivatives for the Treatment of Arrhythmias. WO2008008022, 17 January 2008.
-
(2008)
Isoindoline Derivatives for the Treatment of Arrhythmias
-
-
Bjoere, A.1
Bostroem, J.2
Davidsson, O.3
Emtenaes, H.4
Gran, H.5
Iliefski, T.6
Kajanus, J.7
Olsson, R.8
Sandberg, L.9
Strandlund, G.10
-
10
-
-
0027257652
-
Selective non-nucleoside HIV-1 reverse transcriptase inhibitors. New 2, 3-dihydrothiazolo[2, 3-A]isoindol-5(9bH)-ones and Related Compounds with Anti-HIV-1 Activity
-
Mertens, A.; Zilch, J.H.; Konig, B.; Schafer, W.; Poll, T.; Kampe, W.; Seidel, S.; Leser, U.; Leinert, H. Selective Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors. New 2, 3-Dihydrothiazolo[2, 3-A]isoindol-5(9bH)-ones and Related Compounds with Anti-HIV-1 Activity. J. Med. Chem. 1993, 36, 2526-2535.
-
(1993)
J. Med. Chem
, vol.36
, pp. 2526-2535
-
-
Mertens, A.1
Zilch, J.H.2
Konig, B.3
Schafer, W.4
Poll, T.5
Kampe, W.6
Seidel, S.7
Leser, U.8
Leinert, H.9
-
11
-
-
84983449610
-
-
WO2008156816, 27 March
-
Baldwin, J.J.; Claremon, D.A.; Tice, C.M.; Cacatian, S.; Dillard, L.H.; Ishchenko, A.V.; Yuan, J.; Xu, Z.; Mcgeehan, G.; Zhao, W.; et al. Renin Inhibitors. WO2008156816, 27 March 2008.
-
(2008)
Renin Inhibitors
-
-
Baldwin, J.J.1
Claremon, D.A.2
Tice, C.M.3
Cacatian, S.4
Dillard, L.H.5
Ishchenko, A.V.6
Yuan, J.7
Xu, Z.8
Mcgeehan, G.9
Zhao, W.10
-
12
-
-
84871943641
-
Total spontaneous resolution by deracemization of isoindolinones
-
Yagishita, F.; Ishikawa, H.; Onuki, T.; Hachiya, S.; Mino, T.; Sakamoto, M. Total spontaneous resolution by deracemization of isoindolinones. Angew. Chem. Int. Ed. 2012, 51, 13023-13025.
-
(2012)
Angew. Chem. Int. Ed
, vol.51
, pp. 13023-13025
-
-
Yagishita, F.1
Ishikawa, H.2
Onuki, T.3
Hachiya, S.4
Mino, T.5
Sakamoto, M.6
-
13
-
-
0032537535
-
Isoindolinone enantiomers having affinity for the dopamine D4 receptor
-
Belliotti, T.R.; Brink, W.A.; Kestern, S.R.; Rubin, J.R.; Wistrow, D.J.; Zoski, K.T.; Whetzel, S.Z.; Corbin, A.E.; Pugsley, A.T.; Heffner, T.G.; et al. Isoindolinone enantiomers having affinity for the dopamine D4 receptor. Bioorg. Med. Chem. Lett. 1998, 8, 1499-1502.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 1499-1502
-
-
Belliotti, T.R.1
Brink, W.A.2
Kestern, S.R.3
Rubin, J.R.4
Wistrow, D.J.5
Zoski, K.T.6
Whetzel, S.Z.7
Corbin, A.E.8
Pugsley, A.T.9
Heffner, T.G.10
-
14
-
-
36849081787
-
Novel water-soluble sedative-hypnotic agents: Isoindolin-1-one derivatives
-
Kanamitsu, N.; Osaki, T.; Itsuji, Y.; Yoshimura, M.; Tsujimoto, H.; Soga, M. Novel water-soluble sedative-hypnotic agents: Isoindolin-1-one derivatives. Chem. Pharm. Bull. 2007, 55, 1682-1688.
-
(2007)
Chem. Pharm. Bull
, vol.55
, pp. 1682-1688
-
-
Kanamitsu, N.1
Osaki, T.2
Itsuji, Y.3
Yoshimura, M.4
Tsujimoto, H.5
Soga, M.6
-
15
-
-
38349022144
-
And complementary approaches to the asymmetric synthesis of C3 substituted NH free or N-substituted isoindolin-1-one
-
Lamblin, M.; Couture, A.; Deniau, E.; Grandclaudon, P. Alternative and complementary approaches to the asymmetric synthesis of C3 substituted NH free or N-substituted isoindolin-1-one. Tetrahedron: Asymmetry 2008, 19, 111-123.
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 111-123
-
-
Lamblin, M.1
Couture, A.2
Deniau, E.3
Alternative, G.P.4
-
16
-
-
79956070576
-
Efficient access to (1H)-isoindolin-1-one-3-carboxylic acid derivatives by orthopalladation and carbonylation of methyl arylglycinate substrates
-
Nieto, S.; Sayago, F.J.; Laborda, P.; Soler, T.; Cativiela, C.; Urriolabeitia, E.P. Efficient access to (1H)-isoindolin-1-one-3-carboxylic acid derivatives by orthopalladation and carbonylation of methyl arylglycinate substrates. Tetrahedron 2011, 67, 4185-4191.
-
(2011)
Tetrahedron
, vol.67
, pp. 4185-4191
-
-
Nieto, S.1
Sayago, F.J.2
Laborda, P.3
Soler, T.4
Cativiela, C.5
Urriolabeitia, E.P.6
-
17
-
-
67650087558
-
Complementary synthetic approaches to constitutionally diverse N-Amino-Alkylated isoindolinones: Application to the synthesis of falipamil and 5-HT1A receptor ligand analogues
-
Lorion, M.; Couture, A.; Deniau, E.; Grandclaudon, P. Complementary synthetic approaches to constitutionally diverse N-Amino-Alkylated isoindolinones: Application to the synthesis of falipamil and 5-HT1A receptor ligand analogues. Synthesis 2009, 2009, 1897-1903.
-
(2009)
Synthesis
, vol.2009
, pp. 1897-1903
-
-
Lorion, M.1
Couture, A.2
Deniau, E.3
Grandclaudon, P.4
-
18
-
-
77950479228
-
Diastereo-And enantioselective catalytic tandem michael addition/mannich reaction: Access to chiral isoindolinones and azetidines with multiple stereocenters
-
Guo, S.; Xie, Y.; Hu, X.; Xia, C.; Huang, H. Diastereo-And Enantioselective Catalytic Tandem Michael Addition/Mannich Reaction: Access to Chiral Isoindolinones and Azetidines with Multiple Stereocenters. Angew. Chem. Int. Ed. 2010, 49, 2728-2731.
-
(2010)
Angew. Chem. Int. Ed
, vol.49
, pp. 2728-2731
-
-
Guo, S.1
Xie, Y.2
Hu, X.3
Xia, C.4
Huang, H.5
-
19
-
-
84865842060
-
An asymmetric aerobic aza-wacker-Type cyclization: Synthesis of isoindolinones bearing tetrasubstituted carbon stereocenters
-
Yang, G.; Shen, C.; Zhang, W. An Asymmetric Aerobic Aza-Wacker-Type Cyclization: Synthesis of Isoindolinones Bearing Tetrasubstituted Carbon Stereocenters. Angew. Chem. Int. Ed. 2012, 51, 9141-9145.
-
(2012)
Angew. Chem. Int. Ed
, vol.51
, pp. 9141-9145
-
-
Yang, G.1
Shen, C.2
Zhang, W.3
-
20
-
-
84873389352
-
Hydroxorhodium/chiral diene complexes as effective catalysts for the asymmetric arylation of 3-Aryl-3-hydroxyisoindolin-1-ones
-
Nishimura, T.; Noishiki, A.; Ebe, Y.; Hayashi, T. Hydroxorhodium/Chiral Diene Complexes as Effective Catalysts for the Asymmetric Arylation of 3-Aryl-3-hydroxyisoindolin-1-ones. Angew. Chem. Int. Ed. 2013, 52, 1777-1780.
-
(2013)
Angew. Chem. Int. Ed
, vol.52
, pp. 1777-1780
-
-
Nishimura, T.1
Noishiki, A.2
Ebe, Y.3
Hayashi, T.4
-
21
-
-
79956372069
-
Organocatalyzed enantioselective synthesis of quaternary carbon-containing isoindolin-1-ones
-
Yu, X.; Lu, A.; Wang, Y.; Wu, G.; Song, H.; Zhou, Z.; Tang, C. Organocatalyzed Enantioselective Synthesis of Quaternary Carbon-Containing Isoindolin-1-ones. Eur. J. Org. Chem. 2011, 16, 3060-3066.
-
(2011)
Eur. J. Org. Chem
, vol.16
, pp. 3060-3066
-
-
Yu, X.1
Lu, A.2
Wang, Y.3
Wu, G.4
Song, H.5
Zhou, Z.6
Tang, C.7
-
22
-
-
84861964083
-
Enantioselective total synthesis of (S)-(+)-lennoxamine through asymmetric hydrogenation mediated by L-proline-Tetrazole ruthenium catalyst
-
Mirabal-Gallardo, Y.; Piérola, J.; Shankaraiah, N.; Santos, L.S. Enantioselective total synthesis of (S)-(+)-lennoxamine through asymmetric hydrogenation mediated by L-proline-Tetrazole ruthenium catalyst. Tetrahedron Lett. 2012, 53, 3672-3675.
-
(2012)
Tetrahedron Lett
, vol.53
, pp. 3672-3675
-
-
Mirabal-Gallardo, Y.1
Piérola, J.2
Shankaraiah, N.3
Santos, L.S.4
-
23
-
-
84863012114
-
Asymmetric hydrogenolysis of racemic tertiary alcohols, 3-substituted 3-hydroxyisoindolin-1-ones
-
Chen, M.W.; Chen, Q.A.; Duan, Y.; Ye, Z.S.; Zhou, Y.G. Asymmetric hydrogenolysis of racemic tertiary alcohols, 3-substituted 3-hydroxyisoindolin-1-ones. Chem. Commun. 2012, 48, 1698-1700.
-
(2012)
Chem. Commun
, vol.48
, pp. 1698-1700
-
-
Chen, M.W.1
Chen, Q.A.2
Duan, Y.3
Ye, Z.S.4
Zhou, Y.G.5
-
24
-
-
84863088848
-
The first organocatalytic asymmetric synthesis of 3-substituted isoindolinones
-
More, V.; Rohlmann, R.; García Mancheño, O.; Petronzi, C.; Palombi, L.; de Rosa, A.; di Mola, A.; Massa, A. The first organocatalytic asymmetric synthesis of 3-substituted isoindolinones. RSC Adv. 2012, 2, 3592-3595.
-
(2012)
RSC Adv
, vol.2
, pp. 3592-3595
-
-
More, V.1
Rohlmann, R.2
García Mancheño, O.3
Petronzi, C.4
Palombi, L.5
De Rosa, A.6
Di Mola, A.7
Massa, A.8
-
25
-
-
84885400833
-
Organocatalysts and sequential asymmetric cascade reactions in the synthesis of functionalized isoindolinones and benzoindolizidinones
-
Tiso, S.; Palombi, L.; Vignes, C.; di Mola, A.; Massa, A. Organocatalysts and sequential asymmetric cascade reactions in the synthesis of functionalized isoindolinones and benzoindolizidinones. RSC Adv. 2013, 3, 19380-19387.
-
(2013)
RSC Adv
, vol.3
, pp. 19380-19387
-
-
Tiso, S.1
Palombi, L.2
Vignes, C.3
Di Mola, A.4
Massa, A.5
-
26
-
-
84866245243
-
Synthesis and reactivity of the 3-substituted isoindolinone framework to assemble highly functionalized related structures
-
Petronzi, C.; Collarile, S.; Croce, G.; Filosa, R.; de Caprariis, P.; Peduto, A.; Palombi, L.; Intintoli, V.; Di Mola, A.; Massa, A. Synthesis and Reactivity of the 3-Substituted Isoindolinone Framework to Assemble Highly Functionalized Related Structures. Eur. J. Org. Chem. 2012, 27, 5357-5365.
-
(2012)
Eur. J. Org. Chem
, vol.27
, pp. 5357-5365
-
-
Petronzi, C.1
Collarile, S.2
Croce, G.3
Filosa, R.4
De Caprariis, P.5
Peduto, A.6
Palombi, L.7
Intintoli, V.8
Di Mola, A.9
Massa, A.10
-
27
-
-
84862560122
-
Electrochemically initiated tandem and sequential conjugate addition processes: One-pot synthesis of diverse functionalized isoindolinones
-
Antico, P.; Capaccio, V.; Di Mola, A.; Massa, A.; Palombi, L. Electrochemically Initiated Tandem and Sequential Conjugate Addition Processes: One-Pot Synthesis of Diverse Functionalized Isoindolinones. Adv. Synth. Catal. 2012, 354, 1717-1724.
-
(2012)
Adv. Synth. Catal
, vol.354
, pp. 1717-1724
-
-
Antico, P.1
Capaccio, V.2
Di Mola, A.3
Massa, A.4
Palombi, L.5
-
28
-
-
84885471547
-
Absolute configuration assignment made easier by the VCD of coupled oscillating carbonyls: The case of (-)-propanedioic acids, 2-(2, 3)-dihydro-3-oxo-1H-isoindol-1-yl)-1, 3-dimethyl ester
-
Massa, A.; Rizzo, P.; Monaco, G.; Zanasi, R. Absolute configuration assignment made easier by the VCD of coupled oscillating carbonyls: The case of (-)-propanedioic acids, 2-(2, 3)-dihydro-3-oxo-1H-isoindol-1-yl)-1, 3-dimethyl ester. Tetrahedron Lett. 2013, 54, 6242-6246.
-
(2013)
Tetrahedron Lett
, vol.54
, pp. 6242-6246
-
-
Massa, A.1
Rizzo, P.2
Monaco, G.3
Zanasi, R.4
-
29
-
-
39849104140
-
Silver-catalyzed spirolactonization: First synthesis of spiroisoindole-γ-methylene-γ-butyrolactones
-
Rammah, M.M.; Othman, M.; Ciamala, K.; Strohmann, C.; Rammah, M.B. Silver-catalyzed spirolactonization: First synthesis of spiroisoindole-γ-methylene-γ-butyrolactones. Tetrahedron 2008, 64, 3505-3516.
-
(2008)
Tetrahedron
, vol.64
, pp. 3505-3516
-
-
Rammah, M.M.1
Othman, M.2
Ciamala, K.3
Strohmann, C.4
Rammah, M.B.5
-
30
-
-
33847623075
-
Organocatalytic asymmetric conjugate additions
-
Almasi, D.; Alonso, D.A.; Najera, C. Organocatalytic asymmetric conjugate additions. Tetrahedron: Asymmetry 2007, 18, 299-365.
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 299-365
-
-
Almasi, D.1
Alonso, D.A.2
Najera, C.3
-
31
-
-
84881609166
-
Direct asymmetric Michael addition of phthalide derivatives to chalcones
-
Luo, J.; Jiang, C.; Wang, H.; Xu, L.W.; Lu, Y. Direct asymmetric Michael addition of phthalide derivatives to chalcones. Tetrahedron Lett. 2013, 54, 5261-5265.
-
(2013)
Tetrahedron Lett
, vol.54
, pp. 5261-5265
-
-
Luo, J.1
Jiang, C.2
Wang, H.3
Xu, L.W.4
Lu, Y.5
-
32
-
-
84861514836
-
Rationally designed amide donors for organocatalytic asymmetric michael reactions
-
Tan, B.; Hernandez-Torres, G.; Barbas, C.F. Rationally Designed Amide Donors for Organocatalytic Asymmetric Michael Reactions. Angew. Chem. Int. Ed. 2012, 51, 5381-5385.
-
(2012)
Angew. Chem. Int. Ed
, vol.51
, pp. 5381-5385
-
-
Tan, B.1
Hernandez-Torres, G.2
Barbas, C.F.3
-
33
-
-
84876234339
-
Recent developments in asymmetric phase-Transfer reactions
-
Shirakawa, S.; Maruoka, K. Recent Developments in Asymmetric Phase-Transfer Reactions. Angew. Chem. Int. Ed. 2013, 52, 4312-4348.
-
(2013)
Angew. Chem. Int. Ed
, vol.52
, pp. 4312-4348
-
-
Shirakawa, S.1
Maruoka, K.2
-
34
-
-
76449115669
-
Enantioselective Michael reaction of β-keto esters organocatalyzed by recoverable Cinchona-derived dimeric ammonium salts
-
Tarv, S.; Chinchilla, R.; Najera, C. Enantioselective Michael reaction of β-keto esters organocatalyzed by recoverable Cinchona-derived dimeric ammonium salts. Tetrahedron: Asymmetry 2009, 20, 2651-2654.
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 2651-2654
-
-
Tarí, S.1
Chinchilla, R.2
Nájera, C.3
-
35
-
-
41849101500
-
Organocatalytic asymmetric conjugate addition to allenic esters and ketones
-
Elsner, P.; Bernardi, L.; Salla, G.D.; Overgaard, J.; Jørgensen, K.A. Organocatalytic Asymmetric Conjugate Addition to Allenic Esters and Ketones. J. Am. Chem. Soc. 2008, 130, 4897-4905.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 4897-4905
-
-
Elsner, P.1
Bernardi, L.2
Salla, G.D.3
Overgaard, J.4
Jørgensen, K.A.5
-
36
-
-
84891402766
-
Cascade reactions of glycine schiff bases and chiral phase transfer catalysts in the synthesis of alpha-Amino acids 3-substituted phthalides or isoindolinones
-
Perillo, M.; Di Mola, A.; Filosa, R.; Palombi, L.; Massa, A. Cascade reactions of glycine Schiff bases and chiral phase transfer catalysts in the synthesis of alpha-Amino acids 3-substituted phthalides or isoindolinones. RSC Adv. 2014, 4, 4239-4246.
-
(2014)
RSC Adv
, vol.4
, pp. 4239-4246
-
-
Perillo, M.1
Di Mola, A.2
Filosa, R.3
Palombi, L.4
Massa, A.5
-
37
-
-
84896732550
-
Syntheses and applications of (thio)urea-containing chiral quaternary ammonium salt catalysts
-
Novacek, J.; Waser, M. Syntheses and Applications of (Thio)Urea-Containing Chiral Quaternary Ammonium Salt Catalysts. Eur. J. Org. Chem. 2014, 4, 802-809.
-
(2014)
Eur. J. Org. Chem
, vol.4
, pp. 802-809
-
-
Novacek, J.1
Waser, M.2
-
38
-
-
84862110216
-
A new family of cinchona-derived bifunctional asymmetric phase-Transfer catalysts: Application to the enantio-And diastereoselective nitro-mannich reaction of amidosulfones
-
Johnson, K.M.; Rattley, M.S.; Sladojevich, F.; Barber, D.M.; Nunez, M.G.; Goldys, A.M.; Dixon, D.J. A New Family of Cinchona-Derived Bifunctional Asymmetric Phase-Transfer Catalysts: Application to the Enantio-And Diastereoselective Nitro-Mannich Reaction of Amidosulfones. Org. Lett. 2012, 10, 2492-2495.
-
(2012)
Org. Lett
, vol.10
, pp. 2492-2495
-
-
Johnson, K.M.1
Rattley, M.S.2
Sladojevich, F.3
Barber, D.M.4
Nunez, M.G.5
Goldys, A.M.6
Dixon, D.J.7
-
39
-
-
84872906479
-
Bifunctional chiral quaternary ammonium salt catalysts: A rapidly emerging class of powerful asymmetric catalysts
-
Novacek, J.; Waser, M. Bifunctional Chiral Quaternary Ammonium Salt Catalysts: A Rapidly Emerging Class of Powerful Asymmetric Catalysts. Eur. J. Org. Chem. 2013, 637-648.
-
(2013)
Eur. J. Org. Chem
, pp. 637-648
-
-
Novacek, J.1
Waser, M.2
-
40
-
-
0035928478
-
Synthesis and application of dimeric Cinchona alkaloid phase-Transfer catalysts:-bis[O(9)-Allylcinchonidinium]-o, m or p-xylene dibromide
-
Jew, S.S.; Jeong, B.S.; Yoo, M.S.; Huh, H.; Park, H.G. Synthesis and application of dimeric Cinchona alkaloid phase-Transfer catalysts:-bis[O(9)-Allylcinchonidinium]-o, m or p-xylene dibromide. Chem. Commun. 2001, 1244-1245, doi:10.1039/B102584H.
-
(2001)
Chem. Commun
, pp. 1244-1245
-
-
Jew, S.S.1
Jeong, B.S.2
Yoo, M.S.3
Huh, H.4
Park, H.G.5
-
41
-
-
84983387213
-
-
145022 A1, 24 November 2011
-
Conn, E.L.; Hepworth, D.; Qi, Y.; Rocke, B.N.; Ruggeri, R.B.; Zhang, Y. 2-Phenyl Benzoylamides. PCT WO 2011/145022 A1, 24 November 2011.
-
(2011)
2-Phenyl Benzoylamides. PCT WO
-
-
Conn, E.L.1
Hepworth, D.2
Qi, Y.3
Rocke, B.N.4
Ruggeri, R.B.5
Zhang, Y.6
-
42
-
-
84937764581
-
Organocatalytic asymmetric synthesis of highly functionalized pyrrolizidines via cascade Michael/hemi-Aminalization reactions of isoindolinones
-
Scorzelli, F.; Di Mola, A.; Croce, G.; Palombi, L.; Massa, A. Organocatalytic asymmetric synthesis of highly functionalized pyrrolizidines via cascade Michael/hemi-Aminalization reactions of isoindolinones. Tetrahedron Lett. 2015, 56, 2787-2790.
-
(2015)
Tetrahedron Lett
, vol.56
, pp. 2787-2790
-
-
Scorzelli, F.1
Di Mola, A.2
Croce, G.3
Palombi, L.4
Massa, A.5
-
43
-
-
33747336252
-
Structure-based drug design of a highly potent CDK1, 2, 4, 6 inhibitor with novel macrocyclic quinoxalin-2-one structure
-
Kawanishi, N.; Sugimoto, T.; Shibata, J.; Nakamura, K.; Masutani, K.; Ikuta, M.; Hirai, H. Structure-based drug design of a highly potent CDK1, 2, 4, 6 inhibitor with novel macrocyclic quinoxalin-2-one structure. Bioorg. Chem. Lett. 2006, 16, 5122-5126.
-
(2006)
Bioorg. Chem. Lett
, vol.16
, pp. 5122-5126
-
-
Kawanishi, N.1
Sugimoto, T.2
Shibata, J.3
Nakamura, K.4
Masutani, K.5
Ikuta, M.6
Hirai, H.7
-
44
-
-
0001184925
-
Facile synthesis of isoindolin-1-ones via palladium catalyzed carbonylative cyclization of 2-bromobenzaldehyde with primary amines
-
Cho, C.S.; Jiang, L.H.; Lee, D.Y.; Shim, S.C. Facile synthesis of isoindolin-1-ones via Palladium Catalyzed Carbonylative Cyclization of 2-bromobenzaldehyde with Primary Amines. Bull. Korean Chem. Soc. 1996, 17, 1095-1096.
-
(1996)
Bull. Korean Chem. Soc
, vol.17
, pp. 1095-1096
-
-
Cho, C.S.1
Jiang, L.H.2
Lee, D.Y.3
Shim, S.C.4
-
45
-
-
84929965166
-
3-carboxylate-substituted isoindolinones in k2co3-catalyzed michael reactions
-
Scorzelli, F.; Di Mola, A.; Palombi, L.; Filosa, R.; Massa, A. 3-Carboxylate-Substituted Isoindolinones in K2CO3-Catalyzed Michael Reactions. Synth. Commun. 2015, doi:10.1080/00397911.2015.1033063.
-
(2015)
Synth. Commun
-
-
Scorzelli, F.1
Di Mola, A.2
Palombi, L.3
Filosa, R.4
Massa, A.5
|