-
1
-
-
0030007650
-
Partially modified retro-inverso pseudopeptides as non-natural ligands for the human class I histocompatibility molecule HLA-A2
-
(a) Guichard, G.; Connan, F.; Graff, R.; Ostankovitch, M.; Muller, S.; Guillet, J.-G.; Choppin, J.; Briand, J.-P. Partially modified retro-inverso pseudopeptides as non-natural ligands for the human class I histocompatibility molecule HLA-A2. J. Med. Chem. 1996, 39, 2030-2039;
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2030-2039
-
-
Guichard, G.1
Connan, F.2
Graff, R.3
Ostankovitch, M.4
Muller, S.5
Guillet, J.-G.6
Choppin, J.7
Briand, J.-P.8
-
2
-
-
0025375074
-
Synthesis, biological testing, and stereochemical assignment of an end group modified retro-inverso bombesin C-terminal nonapeptide
-
(b) Cushman, M.; Jurayj, J. J.; Moyert, J. D. Synthesis, biological testing, and stereochemical assignment of an end group modified retro-inverso bombesin C-terminal nonapeptide. J. Org. Chem. 1990, 55, 3186-3194;
-
(1990)
J. Org. Chem.
, vol.55
, pp. 3186-3194
-
-
Cushman, M.1
Jurayj, J.J.2
Moyert, J.D.3
-
3
-
-
0037330546
-
Nociceptin/orphanin FQ(1-13)NH2 analogues modified in the Phe1-Gly2 peptide bond
-
(c) Guerrini, R.; Rizzi, D.; Zucchini, M.; Tomatis, R.; Regoli, D.; Calo, G.; Salvadori, S. Nociceptin/orphanin FQ(1-13)NH2 analogues modified in the Phe1-Gly2 peptide bond. Bioorg. Med. Chem. Lett. 2003, 13, 365-368.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 365-368
-
-
Guerrini, R.1
Rizzi, D.2
Zucchini, M.3
Tomatis, R.4
Regoli, D.5
Calo, G.6
Salvadori, S.7
-
4
-
-
0037134919
-
Recognition of ten base pairs of DNA by head-to-head hairpin dimers
-
(a) Weyermann, P.; Dervan, P. B. Recognition of ten base pairs of DNA by head-to-head hairpin dimers. J. Am. Chem. Soc. 2002, 124, 6872-6878;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 6872-6878
-
-
Weyermann, P.1
Dervan, P.B.2
-
5
-
-
77951292525
-
Novel cationic lipids based on malonic acid amides backbone: Transfection efficacy and cell toxicity properties
-
(b) Heinze, M.; Brzesinski, G.; Dobner, B.; Langner, A. Novel cationic lipids based on malonic acid amides backbone: Transfection efficacy and cell toxicity properties. Bioconjugate Chem. 2010, 21, 696-708.
-
(2010)
Bioconjugate Chem.
, vol.21
, pp. 696-708
-
-
Heinze, M.1
Brzesinski, G.2
Dobner, B.3
Langner, A.4
-
6
-
-
0345377476
-
L-Lysine based gemini organogelators: Their organogelation properties and thermally stable organogels
-
Suzuki, M.; Nigawara, T.; Yumoto, M.; Kimura, M.; Shirai, H.; Hanabusa, K. L-Lysine based gemini organogelators: Their organogelation properties and thermally stable organogels. Org. Biomol. Chem. 2003, 1, 4124-4131.
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 4124-4131
-
-
Suzuki, M.1
Nigawara, T.2
Yumoto, M.3
Kimura, M.4
Shirai, H.5
Hanabusa, K.6
-
7
-
-
34250088882
-
Synthesis of N,N′-diacyl bisglutamic acid derivatives and their influence on the receptor binding of 3H-L-glutamate
-
(a) Kudryashova, N. I.; Gorodinski, A. I.; Dambinova, S. A. Synthesis of N,N′-diacyl bisglutamic acid derivatives and their influence on the receptor binding of 3H-L-glutamate. Pharm. Chem. J. 1987, 21, 390-393;
-
(1987)
Pharm. Chem. J.
, vol.21
, pp. 390-393
-
-
Kudryashova, N.I.1
Gorodinski, A.I.2
Dambinova, S.A.3
-
8
-
-
0035938402
-
Dimeric L-dopa derivatives as potential prodrugs
-
(b) Stefano, A.; Mosciatti, B.; Cingolani, G. M.; Giorgioni, G.; Ricciutelli, M.; Cacciatore, I.; Sozio, P.; Claudi, F. Dimeric L-dopa derivatives as potential prodrugs. Bioorg. Med. Chem. Lett. 2001, 11, 1085-1088.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1085-1088
-
-
Stefano, A.1
Mosciatti, B.2
Cingolani, G.M.3
Giorgioni, G.4
Ricciutelli, M.5
Cacciatore, I.6
Sozio, P.7
Claudi, F.8
-
9
-
-
38949179549
-
Cyclotetrapeptide mimics based on a 13-membered, partially modified retro-inverso structure
-
(a) Gentilucci, L.; Cardillo, G.; Tolomelli, A.; Spampinato, S.; Sparta, A.; Squassabia, F. Cyclotetrapeptide mimics based on a 13-membered, partially modified retro-inverso structure. Eur. J. Org. Chem. 2008, 4, 729-735;
-
(2008)
Eur. J. Org. Chem.
, vol.4
, pp. 729-735
-
-
Gentilucci, L.1
Cardillo, G.2
Tolomelli, A.3
Spampinato, S.4
Sparta, A.5
Squassabia, F.6
-
10
-
-
0037166713
-
Spontaneous macrocyclization of l-cysteine with malononitrile
-
(b) Gilbert, L.; Gonzalez, A.; Granell, J.; Lopez, C. Spontaneous macrocyclization of l-cysteine with malononitrile. Tetrahedron: Asymmetry 2002, 13, 983-988;
-
(2002)
Tetrahedron: Asymmetry
, vol.13
, pp. 983-988
-
-
Gilbert, L.1
Gonzalez, A.2
Granell, J.3
Lopez, C.4
-
11
-
-
0035968957
-
Efficient synthesis of macrocycles by oxidation of cysteine-based dithiols
-
(c) Kudo, H.; Sanda, F.; Endo, T. Efficient synthesis of macrocycles by oxidation of cysteine-based dithiols. Tetrahedron: Lett. 2001, 42, 7847-7850.
-
(2001)
Tetrahedron: Lett.
, vol.42
, pp. 7847-7850
-
-
Kudo, H.1
Sanda, F.2
Endo, T.3
-
12
-
-
0035691917
-
Synthesis and antiinflammatory and analgesic activity of N-[2-(p-hydroxyphenyl)-1,1-dialkylethyl]malonamic acid esters and hydrazides
-
(a) Glushkov, V. A.; Ausheva, O. G.; Anikina, L. V.; Vikharev, Y. B.; Safin, V. A.; Shklyaev, Y. V. Synthesis and antiinflammatory and analgesic activity of N-[2-(p-hydroxyphenyl)-1,1-dialkylethyl]malonamic acid esters and hydrazides. Pharmaceut. Chem. J. 2001, 35, 358-363;
-
(2001)
Pharmaceut. Chem. J.
, vol.35
, pp. 358-363
-
-
Glushkov, V.A.1
Ausheva, O.G.2
Anikina, L.V.3
Vikharev, Y.B.4
Safin, V.A.5
Shklyaev, Y.V.6
-
13
-
-
0022350714
-
Syntheses and antiinflammatory activity of malonamic acid, malonamate, and malonamide derivatives of some heterocyclic compounds
-
(b) Katagi, T.; Aoki, M.; Kashiwagi, M.; Dhata, K.; Kohno, S.; Murata, T.; Inoi, T. Syntheses and antiinflammatory activity of malonamic acid, malonamate, and malonamide derivatives of some heterocyclic compounds. Chem. Pharm. Bull. 1985, 33, 4878-4888.
-
(1985)
Chem. Pharm. Bull.
, vol.33
, pp. 4878-4888
-
-
Katagi, T.1
Aoki, M.2
Kashiwagi, M.3
Dhata, K.4
Kohno, S.5
Murata, T.6
Inoi, T.7
-
16
-
-
0037855196
-
Organic reactions in liquid hydrogen fluoride, II: Synthesis of imidoyl fluorides and N,N′-dialkyl-2-alkylaminomalonamides
-
(a) Norell, J. R. Organic reactions in liquid hydrogen fluoride, II: Synthesis of imidoyl fluorides and N,N′-dialkyl-2-alkylaminomalonamides. J. Org. Chem. 1970, 35, 1619-1625;
-
(1970)
J. Org. Chem.
, vol.35
, pp. 1619-1625
-
-
Norell, J.R.1
-
17
-
-
0013945965
-
Pteridinecar-boxamide diuretics, I: Reaction of 4,6-diamino-5- nitrosopyrimidines with substituted malonamides
-
(b) Osdene, T. S.; Santilli, A. A.; McCardle, L. E.; Rosenthale, M. E. Pteridinecar-boxamide diuretics, I: Reaction of 4,6-diamino-5-nitrosopyrimidines with substituted malonamides. J. Med. Chem. 1966, 9, 697-701.
-
(1966)
J. Med. Chem.
, vol.9
, pp. 697-701
-
-
Osdene, T.S.1
Santilli, A.A.2
McCardle, L.E.3
Rosenthale, M.E.4
-
18
-
-
44649189776
-
Highly efficient selective monohydrolysis of dialkyl malonates and their derivatives
-
(a) Niwayama, S.; Cho, H.; Lin, C. Highly efficient selective monohydrolysis of dialkyl malonates and their derivatives. Tetrahedron Lett. 2008, 49, 4434-4436;
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 4434-4436
-
-
Niwayama, S.1
Cho, H.2
Lin, C.3
-
19
-
-
0001060227
-
Intramolecular nitrogen-hydrogen, oxygen-hydrogen, and sulfur-hydrogen insertion reactions: Synthesis of heterocycles from α-diazo β-keto esters
-
(b) Moyer, M.; Feldman, P. L.; Rapoport, H. Intramolecular nitrogen-hydrogen, oxygen-hydrogen, and sulfur-hydrogen insertion reactions: Synthesis of heterocycles from α-diazo β-keto esters. J. Org. Chem. 1985, 50, 5223-5230;
-
(1985)
J. Org. Chem.
, vol.50
, pp. 5223-5230
-
-
Moyer, M.1
Feldman, P.L.2
Rapoport, H.3
-
20
-
-
33846117931
-
New competitive inhibitors of cytosolic (NADH-dependent) rabbit muscle glycerophosphate dehydrogenas
-
(c) Fonvielle, M.; Therisod, H.; Hemery, M.; Therisod, M. New competitive inhibitors of cytosolic (NADH-dependent) rabbit muscle glycerophosphate dehydrogenas. Bioorg. Med. Chem. Lett. 2007, 17, 410-413;
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 410-413
-
-
Fonvielle, M.1
Therisod, H.2
Hemery, M.3
Therisod, M.4
-
21
-
-
0025188103
-
Reaction of aldehydes with stabilized sulfur ylides: Highly stereoselective synthesis of 2,3-epoxy-amides
-
(d) Fernandez, M. V.; Durante-Lane, P.; Lopez-Herrera, F. J. Reaction of aldehydes with stabilized sulfur ylides: Highly stereoselective synthesis of 2,3-epoxy-amides. Tetrahedron 1990, 46, 7911-7922;
-
(1990)
Tetrahedron
, vol.46
, pp. 7911-7922
-
-
Fernandez, M.V.1
Durante-Lane, P.2
Lopez-Herrera, F.J.3
-
22
-
-
0022350714
-
Syntheses and antiinflammatory activity of malonamic acid, malonamate and malonamide derivatives of some heterocyclic compounds
-
(e) Katagi, T.; Aoki, M.; Kashiwagi, M.; Ohata, K.; Kohno, S. Syntheses and antiinflammatory activity of malonamic acid, malonamate and malonamide derivatives of some heterocyclic compounds. Chem. Pharm. Bull. 1985, 33, 4878-4888;
-
(1985)
Chem. Pharm. Bull.
, vol.33
, pp. 4878-4888
-
-
Katagi, T.1
Aoki, M.2
Kashiwagi, M.3
Ohata, K.4
Kohno, S.5
-
23
-
-
33645010150
-
New indium-mediated cyclisation reactions of tethered haloenynes in aqueous solvent systems
-
(f) Goeta, A.; Salter, M. M.; Shah, H. New indium-mediated cyclisation reactions of tethered haloenynes in aqueous solvent systems. Tetrahedron 2006, 62, 3582-3599;
-
(2006)
Tetrahedron
, vol.62
, pp. 3582-3599
-
-
Goeta, A.1
Salter, M.M.2
Shah, H.3
-
24
-
-
62949142162
-
The highly enantioselective phase-transfer catalytic mono-alkylation of malonamic esters
-
(g) Kim, M. H.; Choi, S. H.; Lee, Y. J.; Lee, J.; Park, H. G.; Jew, S. S.; Nahm, K.; Jeong, B. S. The highly enantioselective phase-transfer catalytic mono-alkylation of malonamic esters. Chem. Commun. 2009, 7, 782-784;
-
(2009)
Chem. Commun.
, vol.7
, pp. 782-784
-
-
Kim, M.H.1
Choi, S.H.2
Lee, Y.J.3
Lee, J.4
Park, H.G.5
Jew, S.S.6
Nahm, K.7
Jeong, B.S.8
-
25
-
-
33750007360
-
Foldamer-based pyridine-fullerene tweezer receptors for enhanced binding of zinc porphyrin
-
(h) Zong-Quan, W.; Chang-Zhi, L.; Dai-Jun, F.; Xi-Kui, J.; Zhan-Ting, L. Foldamer-based pyridine-fullerene tweezer receptors for enhanced binding of zinc porphyrin. Tetrahedron 2006, 62, 11054-11062;
-
(2006)
Tetrahedron
, vol.62
, pp. 11054-11062
-
-
Zong-Quan, W.1
Chang-Zhi, L.2
Dai-Jun, F.3
Xi-Kui, J.4
Zhan-Ting, L.5
-
26
-
-
33847620336
-
Novel malonamide derivatives as potent j opioid receptor agonists
-
(i) Chu, G. H.; Gu, M.; Cassel, J. A.; Belanger, S.; Graczyk, T. M.; DeHaven, R. M. Conway-James, N.; Koblish, M.; Little, P. J.; DeHaven-Hudkinsb, D. J.; Dollea, R. E. Novel malonamide derivatives as potent j opioid receptor agonists. Bioorg. Med. Chem. Lett. 2007, 17, 1951-1955.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 1951-1955
-
-
Chu, G.H.1
Gu, M.2
Cassel, J.A.3
Belanger, S.4
Graczyk, T.M.5
DeHaven, R.M.6
Conway-James, N.7
Koblish, M.8
Little, P.J.9
DeHaven-Hudkinsb, D.J.10
Dollea, R.E.11
-
27
-
-
0035797069
-
Versatile synthesis of malonamic acid derivatives from a β-ketothioester
-
Lopez-Alvaradoa, P.; Avendano, C; Menendez, J. C. Versatile synthesis of malonamic acid derivatives from a β-ketothioester. Tetrahedron Lett. 2001, 42, 4479-4482.
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 4479-4482
-
-
Lopez-Alvaradoa, P.1
Avendano, C.2
Menendez, J.C.3
-
28
-
-
38949179549
-
Cyclotetrapeptide mimics based on a 13-membered, partially modified retro-inverso structure
-
(a) Gentilucci, L.; Cardillo, G.; Tolomelli, A.; Spampinato, S.; Sparta, A.; Squassabia, F. Cyclotetrapeptide mimics based on a 13-membered, partially modified retro-inverso structure. Eur. J. Org. Chem. 2008, 4, 729-735;
-
(2008)
Eur. J. Org. Chem.
, vol.4
, pp. 729-735
-
-
Gentilucci, L.1
Cardillo, G.2
Tolomelli, A.3
Spampinato, S.4
Sparta, A.5
Squassabia, F.6
-
29
-
-
35649004955
-
Solution-phase parallel synthesis of dissymmetric disubstituted malonamides carrying amino ester residues
-
(b) Fioravanti, S.; Morreale, A.; Pellacani, L.; Ramadori, F.; Tardella, P. A. Solution-phase parallel synthesis of dissymmetric disubstituted malonamides carrying amino ester residues. Synlett 2007, 17, 2759-2762.
-
(2007)
Synlett
, vol.17
, pp. 2759-2762
-
-
Fioravanti, S.1
Morreale, A.2
Pellacani, L.3
Ramadori, F.4
Tardella, P.A.5
-
30
-
-
0000802654
-
Conformation-directing effects of a single intramolecular amide-amide hydrogen bond: Variable-temperature NMR and IR studies on a homologous diamide series
-
(a) Gellman, S. H.; Dado, G. P.; Liang, G. B.; Adams, B. R. Conformation-directing effects of a single intramolecular amide-amide hydrogen bond: Variable-temperature NMR and IR studies on a homologous diamide series. J. Am. Chem. Soc. 1991, 113, 1164-1173;
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 1164-1173
-
-
Gellman, S.H.1
Dado, G.P.2
Liang, G.B.3
Adams, B.R.4
-
31
-
-
0036416729
-
A new β-keto amide synthesis
-
(b) Chen, Y.; Sieburth, S. M. A new β-keto amide synthesis. Synthesis 2002, 15, 2191-2195.
-
(2002)
Synthesis
, vol.15
, pp. 2191-2195
-
-
Chen, Y.1
Sieburth, S.M.2
-
32
-
-
0037204009
-
Synthesis and biological activity of a novel class of small molecular weight peptidomimetic competitive inhibitors of protein tyrosine phosphatase 1B
-
(a) Larsen, S. D.; Barf, T.; Liljebris, C; May, P. D.; Ogg, D.; O'Sullivan, T. J.; Palazuk, B. J.; Schostarez, H. J.; Stevens, F. C; Bleasdale, J. E. Synthesis and biological activity of a novel class of small molecular weight peptidomimetic competitive inhibitors of protein tyrosine phosphatase 1B. J. Med. Chem. 2002, 45, 598-622;
-
(2002)
J. Med. Chem.
, vol.45
, pp. 598-622
-
-
Larsen, S.D.1
Barf, T.2
Liljebris, C.3
May, P.D.4
Ogg, D.5
O'Sullivan, T.J.6
Palazuk, B.J.7
Schostarez, H.J.8
Stevens, F.C.9
Bleasdale, J.E.10
-
33
-
-
20144383383
-
Novel cyclopentane dicarboxamide sodium channel blockers as a potential treatment for chronic pain
-
(b) Shao, P. P.; Ok, D.; Fisher, M. H.; Garcia, M. L.; Kaczorowski, G. J.; Li, C; Lyons, K. A.; Martin, W. J.; Meinke, P. T.; Priest, B. T.; Smith, M. M.; Wyvratt, M. J.; Ye, F.; Parsons, W. H. Novel cyclopentane dicarboxamide sodium channel blockers as a potential treatment for chronic pain. Bioorg. Med. Chem. Lett. 2005, 15, 1901-1907.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 1901-1907
-
-
Shao, P.P.1
Ok, D.2
Fisher, M.H.3
Garcia, M.L.4
Kaczorowski, G.J.5
Li, C.6
Lyons, K.A.7
Martin, W.J.8
Meinke, P.T.9
Priest, B.T.10
Smith, M.M.11
Wyvratt, M.J.12
Ye, F.13
Parsons, W.H.14
-
34
-
-
5644289358
-
Mechanistic evidence for an α-oxoketene pathway in the formation of β-ketoamides/esters via Meldrum's acid adducts
-
(a) Xu, F.; Armstrong, J. D.; Zhou, G. X.; Simmons, B.; Hughes, D.; Ge, Z.; Grabowski, E. J. J. Mechanistic evidence for an α-oxoketene pathway in the formation of β-ketoamides/esters via Meldrum's acid adducts. J. Am. Chem. Soc. 2004, 126, 13002-13009;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 13002-13009
-
-
Xu, F.1
Armstrong, J.D.2
Zhou, G.X.3
Simmons, B.4
Hughes, D.5
Ge, Z.6
Grabowski, E.J.J.7
-
35
-
-
0004351529
-
Convenient preparation of trifluoroacetyl Meldrum's acid and its use as a building block for trifluoromethyl-containing compounds
-
(b) Morita, Y.; Kamakura, R.; Takeda, M.; Yamamoto, Y. Convenient preparation of trifluoroacetyl Meldrum's acid and its use as a building block for trifluoromethyl-containing compounds. Chem. Commun. 1997, 4, 359-360;
-
(1997)
Chem. Commun.
, vol.4
, pp. 359-360
-
-
Morita, Y.1
Kamakura, R.2
Takeda, M.3
Yamamoto, Y.4
-
36
-
-
0001442454
-
1,3-Oxazines and related compounds, XIII: Reaction of acyl Meldrum's acids with Schiff bases giving 2,3-disubstituted 5-acy1-3,4,5,6-tetrahydro-2H-1, 3-oxazine-4,6-diones and 2,3,6-trisubstituted 2,3-dihydro-1,3-oxazin-4-ones
-
(c) Yamamoto, Y.; Watanabe, Y.; Ohnishi, S. 1,3-Oxazines and related compounds, XIII: Reaction of acyl Meldrum's acids with Schiff bases giving 2,3-disubstituted 5-acy1-3,4,5,6-tetrahydro-2H-1,3-oxazine-4,6-diones and 2,3,6-trisubstituted 2,3-dihydro-1,3-oxazin-4-ones. Chem. Pharm. Bull. 1987, 35, 1860-1870;
-
(1987)
Chem. Pharm. Bull.
, vol.35
, pp. 1860-1870
-
-
Yamamoto, Y.1
Watanabe, Y.2
Ohnishi, S.3
-
37
-
-
0011809376
-
1,3-Oxazines and related compounds, XIV: Facile synthesis of 2,3,6-trisubstituted 2,3-dihydro-1,3-oxazine-5-carboxylic acids and 1,4-disubstituted 3-acyl-β-lactams from acyl Meldrum's acids and Schiff bases
-
(d) Yamamoto, Y.; Watanabe, Y. 1,3-Oxazines and related compounds, XIV: Facile synthesis of 2,3,6-trisubstituted 2,3-dihydro-1,3-oxazine-5-carboxylic acids and 1,4-disubstituted 3-acyl-β-lactams from acyl Meldrum's acids and Schiff bases. Chem. Pharm. Bull. 1987, 35, 1871-1878;
-
(1987)
Chem. Pharm. Bull.
, vol.35
, pp. 1871-1878
-
-
Yamamoto, Y.1
Watanabe, Y.2
-
38
-
-
0034712155
-
A novel route to 5-substituted 3-isoxazolols: Cyclization of N,O-DiBoc β-keto hydroxamic acids synthesized via acyl Meldrum's acids
-
(e) Sorensen, U. S.; Falch, E.; Krogsgaard-Larsen, P. A novel route to 5-substituted 3-isoxazolols: Cyclization of N,O-DiBoc β-keto hydroxamic acids synthesized via acyl Meldrum's acids. J. Org. Chem. 2000, 65, 1003-1007;
-
(2000)
J. Org. Chem.
, vol.65
, pp. 1003-1007
-
-
Sorensen, U.S.1
Falch, E.2
Krogsgaard-Larsen, P.3
-
39
-
-
0035812804
-
An enantioselective ketene - Imine cycloaddition method for synthesis of substituted ring-fused 2-pyridinones
-
(f) Emtenas, H.; Alderin, L.; Almqvist, F. An enantioselective ketene - imine cycloaddition method for synthesis of substituted ring-fused 2-pyridinones. J. Org. Chem. 2001, 66, 6756-6761.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 6756-6761
-
-
Emtenas, H.1
Alderin, L.2
Almqvist, F.3
-
40
-
-
0002306137
-
Convenient synthesis of unsymmetric N,N′-disubstituted malondiamides mediated by Meldrum's acid
-
Lee, H. L.; Lee, J. P.; Lee, G. H.; Pak, C. S. Convenient synthesis of unsymmetric N,N′-disubstituted malondiamides mediated by Meldrum's acid. Synlett 1996, 12, 1209-1210.
-
(1996)
Synlett
, vol.12
, pp. 1209-1210
-
-
Lee, H.L.1
Lee, J.P.2
Lee, G.H.3
Pak, C.S.4
-
41
-
-
0033998176
-
Enols of carboxylic acid amides with β-electron-withdrawing substituents
-
Mukhopadhyaya, J. K.; Sklenák, S.; Rappoport, Z. Enols of carboxylic acid amides with β-electron-withdrawing substituents. J. Am. Chem. Soc. 2000, 122, 1325-1336.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 1325-1336
-
-
Mukhopadhyaya, J.K.1
Sklenák, S.2
Rappoport, Z.3
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