-
1
-
-
0035413618
-
MAP kinases
-
Chen Z, Gibson TB, Robinson F, Silvestro L, Pearson Q, Xu B, Wright A, Vanderbilt C, Cobb MH: MAP kinases. Chem Rev (2001) 101(8):2449-2476.
-
(2001)
Chem Rev
, vol.101
, Issue.8
, pp. 2449-2476
-
-
Chen, Z.1
Gibson, T.B.2
Robinson, F.3
Silvestro, L.4
Pearson, Q.5
Xu, B.6
Wright, A.7
Vanderbilt, C.8
Cobb, M.H.9
-
2
-
-
27744561133
-
p38 MAP kinase inhibitors: Metabolically stabilized pipeline-substituted quinolinones and naphthyridinones
-
Bao J, Hunt JA, Miao S, Rupprecht KM, Stelmach JE, Liu L, Ruzek RD, Sinclair PJ, Pivnichny JV, Hop CE, Kumar S et al: p38 MAP kinase inhibitors: Metabolically stabilized pipeline-substituted quinolinones and naphthyridinones. Bioorg Med Chem Lett (2005) 16(1):64-68.
-
(2005)
Bioorg Med Chem Lett
, vol.16
, Issue.1
, pp. 64-68
-
-
Bao, J.1
Hunt, J.A.2
Miao, S.3
Rupprecht, K.M.4
Stelmach, J.E.5
Liu, L.6
Ruzek, R.D.7
Sinclair, P.J.8
Pivnichny, J.V.9
Hop, C.E.10
Kumar, S.11
-
3
-
-
0027761036
-
Bicyclic imidazoles as a novel class of cytokine biosynthesis inhibitors
-
Lee JC, Badger AM, Griswold DE, Dunnington D, Truneh A, Votta B, White JR, Young PR, Bender PE: Bicyclic imidazoles as a novel class of cytokine biosynthesis inhibitors. Ann NY Acad Sci (1993) 696:149-170.
-
(1993)
Ann NY Acad Sci
, vol.696
, pp. 149-170
-
-
Lee, J.C.1
Badger, A.M.2
Griswold, D.E.3
Dunnington, D.4
Truneh, A.5
Votta, B.6
White, J.R.7
Young, P.R.8
Bender, P.E.9
-
4
-
-
0036126438
-
Monocyte intracellular cytokine production during human endotoxaemia with or without a second in vitro LPS challenge: Effect of RWJ-67657, a p38 MAP-kinase inhibitor, on LPS-hyporesponsiveness
-
Faas MM, Moes H, Fijen JW, Muller Kobold AC, Tulleken JE, Zijlstra JG: Monocyte intracellular cytokine production during human endotoxaemia with or without a second in vitro LPS challenge: Effect of RWJ-67657, a p38 MAP-kinase inhibitor, on LPS-hyporesponsiveness. Clin Exp Immunol (2002) 127(2):337-343.
-
(2002)
Clin Exp Immunol
, vol.127
, Issue.2
, pp. 337-343
-
-
Faas, M.M.1
Moes, H.2
Fijen, J.W.3
Muller Kobold, A.C.4
Tulleken, J.E.5
Zijlstra, J.G.6
-
5
-
-
0037090078
-
Anti-inflammatory effects of a p38 mitogen-activated protein kinase inhibitor during human endotoxemia
-
Branger J, van den Blink B, Weijer S, Madwed J, Bos CL, Gupta A, Yong CL, Polmar SH, Olszyna DP, Hack CE, van Deventer SJ et al: Anti-inflammatory effects of a p38 mitogen-activated protein kinase inhibitor during human endotoxemia. J Immunol (2002) 168(8):4070-4077.
-
(2002)
J Immunol
, vol.168
, Issue.8
, pp. 4070-4077
-
-
Branger, J.1
Van Den Blink, B.2
Weijer, S.3
Madwed, J.4
Bos, C.L.5
Gupta, A.6
Yong, C.L.7
Polmar, S.H.8
Olszyna, D.P.9
Hack, C.E.10
Van Deventer, S.J.11
-
6
-
-
0037330941
-
p38 inhibitors: Piperidine- and 4-aminopiperidine-substituted naphthyridinones, quinolinones, and dihydroquinazolinones
-
Hunt JA, Kallashi F, Ruzek RD, Sinclair PJ, Ita I, McCormick SX, Pivnichny JV, Hop CE, Kumar S, Wang Z, O'Keefe SJ et al: p38 Inhibitors: Piperidine- and 4-aminopiperidine-substituted naphthyridinones, quinolinones, and dihydroquinazolinones. Bioorg Med Chem Lett (2003) 13(3):467-470.
-
(2003)
Bioorg Med Chem Lett
, vol.13
, Issue.3
, pp. 467-470
-
-
Hunt, J.A.1
Kallashi, F.2
Ruzek, R.D.3
Sinclair, P.J.4
Ita, I.5
McCormick, S.X.6
Pivnichny, J.V.7
Hop, C.E.8
Kumar, S.9
Wang, Z.10
O'Keefe, S.J.11
-
7
-
-
0141775420
-
An expedient synthesis of highly functionalized naphthyridones and quinolines from a common N-aryl pyridinone template
-
Savarin CG, Murty JA, Dormer PG: An expedient synthesis of highly functionalized naphthyridones and quinolines from a common N-aryl pyridinone template. Org Lett (2002) 4(12):2071-2074.
-
(2002)
Org Lett
, vol.4
, Issue.12
, pp. 2071-2074
-
-
Savarin, C.G.1
Murty, J.A.2
Dormer, P.G.3
-
8
-
-
1442341534
-
The preparation and rearrangement of 2-allyl-1,2-dihydroquinoline
-
Gilman H, Eisch J, Soddy TS: The preparation and rearrangement of 2-allyl-1,2-dihydroquinoline. J Am Chem Soc (1959) 81(15):4000-4003.
-
(1959)
J Am Chem Soc
, vol.81
, Issue.15
, pp. 4000-4003
-
-
Gilman, H.1
Eisch, J.2
Soddy, T.S.3
-
9
-
-
0000363401
-
Regioselective addition of Grignard reagents to 1-acylpyridinium salts. A convenient method for the synthesis of 4-alkyl(aryl)pyridines
-
Comins DL, Abdullah AH: Regioselective addition of Grignard reagents to 1-acylpyridinium salts. A convenient method for the synthesis of 4-alkyl(aryl)pyridines. J Org Chem (1982) 47(22):4315-4319.
-
(1982)
J Org Chem
, vol.47
, Issue.22
, pp. 4315-4319
-
-
Comins, D.L.1
Abdullah, A.H.2
-
10
-
-
0001594209
-
Regioselective addition of Grignard reagents to the 1-phenoxycarbonyl salts of alkyl nicotinates
-
Comins DL, Stroud ED, Herrick JJ: Regioselective addition of Grignard reagents to the 1-phenoxycarbonyl salts of alkyl nicotinates. Heterocycles (1984) 22(1):151-157.
-
(1984)
Heterocycles
, vol.22
, Issue.1
, pp. 151-157
-
-
Comins, D.L.1
Stroud, E.D.2
Herrick, J.J.3
-
11
-
-
0000366906
-
Synthesis and synthetic utility of 1-acyl-5-(trialkylsilyl)-1,2- dihydropyridines. A synthesis of (±)-elaeokanine A
-
Comins DL, Myoung YC: Synthesis and synthetic utility of 1-acyl-5-(trialkylsilyl)-1,2-dihydropyridines. A synthesis of (±)-elaeokanine A. J Org Chem (1990) 55(1):292-298.
-
(1990)
J Org Chem
, vol.55
, Issue.1
, pp. 292-298
-
-
Comins, D.L.1
Myoung, Y.C.2
-
12
-
-
0003230738
-
A novel ethynylation of pyridines by Reissert-Henze type reaction
-
Nishiwaki N, Minakata S, Komatsu M, Ohshiro Y: A novel ethynylation of pyridines by Reissert-Henze type reaction. Chem Lett (1989) 18(5):773-776.
-
(1989)
Chem Lett
, vol.18
, Issue.5
, pp. 773-776
-
-
Nishiwaki, N.1
Minakata, S.2
Komatsu, M.3
Ohshiro, Y.4
-
13
-
-
0000608835
-
Regioselective synthesis of 2-substituted pyridines via Grignard addition to 1-(alkoxycarboxy)-pyridinium salts
-
Webb TR: Regioselective synthesis of 2-substituted pyridines via Grignard addition to 1-(alkoxycarboxy)-pyridinium salts. Tetrahedron Lett (1985) 26(27):3191-3194.
-
(1985)
Tetrahedron Lett
, vol.26
, Issue.27
, pp. 3191-3194
-
-
Webb, T.R.1
-
14
-
-
0000564686
-
Regioselective organometallic synthesis of pyridines, 4-picolines, and 3,5-lutidines substituted in the 2-position by an unsaturated and/or functional group
-
Al-Amaout A, Courtois G, Miginiac L: Regioselective organometallic synthesis of pyridines, 4-picolines, and 3,5-lutidines substituted in the 2-position by an unsaturated and/or functional group. J Organometallic Chem (1987) 333(2):139-153.
-
(1987)
J Organometallic Chem
, vol.333
, Issue.2
, pp. 139-153
-
-
Al-Amaout, A.1
Courtois, G.2
Miginiac, L.3
-
15
-
-
0033967704
-
Versatile synthesis of 6-alkyl and aryl substituted pyridoxal derivatives
-
Kim Y-C, Jacobson KA: Versatile synthesis of 6-alkyl and aryl substituted pyridoxal derivatives. Synthesis (2000) (1):119-122.
-
(2000)
Synthesis
, Issue.1
, pp. 119-122
-
-
Kim, Y.-C.1
Jacobson, K.A.2
-
16
-
-
0035806298
-
Expeditious preparation of 2-substituted quinolines
-
Fakhfakh MA, Fanck X, Fournet A, Hocquemiller R. Figadere B: Expeditious preparation of 2-substituted quinolines. Tetrahedron Lett (2001) 42(23):3847-3850.
-
(2001)
Tetrahedron Lett
, vol.42
, Issue.23
, pp. 3847-3850
-
-
Fakhfakh, M.A.1
Fanck, X.2
Fournet, A.3
Hocquemiller, R.4
Figadere, B.5
-
17
-
-
0040745792
-
Reaction of pyridine and quinoline N-oxides with phenylmagnesium bromide
-
Kato T, Yamanaka H: Reaction of pyridine and quinoline N-oxides with phenylmagnesium bromide. J Org Chem (1965) 30:910-913.
-
(1965)
J Org Chem
, vol.30
, pp. 910-913
-
-
Kato, T.1
Yamanaka, H.2
-
18
-
-
0008829908
-
Reactions of aryl Grignard reagents with pyridine 1-oxide. Structure of the addition products
-
Kellogg RM, van Bergen TJ: Reactions of aryl Grignard reagents with pyridine 1-oxide. Structure of the addition products. J Org Chem (1971) 36(12):1705-1708.
-
(1971)
J Org Chem
, vol.36
, Issue.12
, pp. 1705-1708
-
-
Kellogg, R.M.1
Van Bergen, T.J.2
-
19
-
-
20444506313
-
Grignard reaction with pyridine-N-oxide
-
Schiess P, Ringele P: Grignard reaction with pyridine-N-oxide. Tetrahedron Lett (1972) 13(4):311-312.
-
(1972)
Tetrahedron Lett
, vol.13
, Issue.4
, pp. 311-312
-
-
Schiess, P.1
Ringele, P.2
-
20
-
-
0000285727
-
Grignard-addition an pyridin-N-oxide
-
Schiess P, Monnier C, Ringele P, Sendi E: Grignard-addition an pyridin-N-oxide. Helv Chim Acta (1974) 57(6):1676-1691.
-
(1974)
Helv Chim Acta
, vol.57
, Issue.6
, pp. 1676-1691
-
-
Schiess, P.1
Monnier, C.2
Ringele, P.3
Sendi, E.4
-
21
-
-
0000608835
-
Regioselective synthesis of 2-substituted pyridines via Grignard addition to 1-(alkoxycarboxy)-pyridinium salts
-
Webb TR: Regioselective synthesis of 2-substituted pyridines via Grignard addition to 1-(alkoxycarboxy)-pyridinium salts. Tetrahedron Lett (1985) 26(27):3191-3194.
-
(1985)
Tetrahedron Lett
, vol.26
, Issue.27
, pp. 3191-3194
-
-
Webb, T.R.1
-
22
-
-
0345388472
-
Enamines. VIII. Reactions of the Grignard reagent with quaternary salts of quinoline N-oxide and lepidine N-oxide
-
Cervinka O, Fabryova A, Matouchova L: Enamines. VIII. Reactions of the Grignard reagent with quaternary salts of quinoline N-oxide and lepidine N-oxide. Coll Czech Chem Comm (1963) 28:535-538.
-
(1963)
Coll Czech Chem Comm
, vol.28
, pp. 535-538
-
-
Cervinka, O.1
Fabryova, A.2
Matouchova, L.3
-
23
-
-
0035806298
-
Expeditious preparation of 2-substituted quinolines
-
Fakhfakh MA, Franck X, Fournet A, Hocquemiller R, Figadere B: Expeditious preparation of 2-substituted quinolines. Tetrahedron Lett (2001) 42(23):3847-3850.
-
(2001)
Tetrahedron Lett
, vol.42
, Issue.23
, pp. 3847-3850
-
-
Fakhfakh, M.A.1
Franck, X.2
Fournet, A.3
Hocquemiller, R.4
Figadere, B.5
-
24
-
-
0018464541
-
Syntheses of nitrogen-containing heterocyclic compounds. XXXVII. On the antimicrobial activity and syntheses of 2-phenylquinoline 1-oxides and phenyl-1,8-naphthyridines
-
author's translation
-
Takeuchi I, Ozawa I, Shigemura K, Hamada Y, Ito T, Ohyama A: [Syntheses of nitrogen-containing heterocyclic compounds. XXXVII. On the antimicrobial activity and syntheses of 2-phenylquinoline 1-oxides and phenyl-1,8- naphthyridines (author's translation)] Yakugaku Zasshi (1979) 99(5):451-457
-
(1979)
Yakugaku Zasshi
, vol.99
, Issue.5
, pp. 451-457
-
-
Takeuchi, I.1
Ozawa, I.2
Shigemura, K.3
Hamada, Y.4
Ito, T.5
Ohyama, A.6
-
25
-
-
0010778743
-
On the reaction mechanism of heteroaromatic N-oxides with 5-hexenylmagnesium bromide
-
Eberson L, Cardellini L, Greci L, Poloni M: On the reaction mechanism of heteroaromatic N-oxides with 5-hexenylmagnesium bromide. Gazz Chim Ital (1988) 118:35-38.
-
(1988)
Gazz Chim Ital
, vol.118
, pp. 35-38
-
-
Eberson, L.1
Cardellini, L.2
Greci, L.3
Poloni, M.4
-
26
-
-
0033214146
-
Reaction of quinoline N-oxides with alkyl- and aryllithiums in the presence of oxidant
-
Tagawa Y, Nomura M, Yamashita H, Goto Y, Hamana M: Reaction of quinoline N-oxides with alkyl- and aryllithiums in the presence of oxidant. Heterocycles (1999) 51(10):2385-2397.
-
(1999)
Heterocycles
, vol.51
, Issue.10
, pp. 2385-2397
-
-
Tagawa, Y.1
Nomura, M.2
Yamashita, H.3
Goto, Y.4
Hamana, M.5
-
27
-
-
84987285019
-
Alkylation of haloquinolines by Grignard reagents with nickel-phosphine complex catalysts
-
Thorsett ED, Stermitz FR: Alkylation of haloquinolines by Grignard reagents with nickel-phosphine complex catalysts. J Heterocycl Chem (1973) 10:243-244.
-
(1973)
J Heterocycl Chem
, vol.10
, pp. 243-244
-
-
Thorsett, E.D.1
Stermitz, F.R.2
-
28
-
-
0037146041
-
Iron-catalyzed cross-coupling reactions
-
Fürstner A, Leitner A, Mendez M, Krause H: Iron-catalyzed cross-coupling reactions. J Am Chem Soc (2002) 124(46):13856-13863.
-
(2002)
J Am Chem Soc
, vol.124
, Issue.46
, pp. 13856-13863
-
-
Fürstner, A.1
Leitner, A.2
Mendez, M.3
Krause, H.4
-
29
-
-
0037083916
-
Iron-catalyzed cross-coupling reactions of alkyl-Grignard reagents with aryl chlorides, tosylates, and triflates
-
Fürstner A, Leitner A: Iron-catalyzed cross-coupling reactions of alkyl-Grignard reagents with aryl chlorides, tosylates, and triflates. Angew Chem-Int Ed (2002) 41(4):609-612.
-
(2002)
Angew Chem-Int Ed
, vol.41
, Issue.4
, pp. 609-612
-
-
Fürstner, A.1
Leitner, A.2
-
30
-
-
0037163328
-
Cyclopropylboronic acid: Synthesis and Suzuki cross-coupling reactions
-
Wallace DJ, Chen C: Cyclopropylboronic acid: Synthesis and Suzuki cross-coupling reactions. Tetrahedron Lett (2002) 43(39):6987-6990.
-
(2002)
Tetrahedron Lett
, vol.43
, Issue.39
, pp. 6987-6990
-
-
Wallace, D.J.1
Chen, C.2
-
32
-
-
3543047335
-
Direct synthesis of 4-arylpiperidines via palladium/copper(I)-cocatalyzed Negishi coupling of a 4-piperidylzinc iodide with aromatic halides and triflates
-
Corley EG, Conrad K, Murry JA, Savarin C, Holko J, Boice G: Direct synthesis of 4-arylpiperidines via palladium/copper(I)-cocatalyzed Negishi coupling of a 4-piperidylzinc iodide with aromatic halides and triflates. J Org Chem (2004) 69(15):5120-5123.
-
(2004)
J Org Chem
, vol.69
, Issue.15
, pp. 5120-5123
-
-
Corley, E.G.1
Conrad, K.2
Murry, J.A.3
Savarin, C.4
Holko, J.5
Boice, G.6
-
33
-
-
11844277647
-
Cobalt-catalyzed cross-coupling reaction of chtoropyridines with Grignard reagents
-
Ohmiya H, Yorimitsu H, Oshima K: Cobalt-catalyzed cross-coupling reaction of chtoropyridines with Grignard reagents. Chem Lett (2004) 33(10):1240-1241.
-
(2004)
Chem Lett
, vol.33
, Issue.10
, pp. 1240-1241
-
-
Ohmiya, H.1
Yorimitsu, H.2
Oshima, K.3
-
34
-
-
85010110760
-
Condensation of diethyl acetonedicarboxylate. IV. Regioselective reaction of diethyl acetonedicarboxylate-magnesium complex
-
Yamato M, Kusunoki Y: Condensation of diethyl acetonedicarboxylate. IV. Regioselective reaction of diethyl acetonedicarboxylate-magnesium complex. Chem Pharm Bull (1981) 29:2832-2836.
-
(1981)
Chem Pharm Bull
, vol.29
, pp. 2832-2836
-
-
Yamato, M.1
Kusunoki, Y.2
-
35
-
-
0020040411
-
Reaction of dimethyl sodio-3-ketoglutarate with glyoxal and substituted glyoxals: First expeditious preparation of bicyclo[3.3.0]octane-3,7-dione; synthesis and crystal structure of 5,7-dihydroxy-4-methoxycarbonyl-3-phenyl-1- indanone
-
Bertz SH, Rihs G, Woodward RB: Reaction of dimethyl sodio-3-ketoglutarate with glyoxal and substituted glyoxals: First expeditious preparation of bicyclo[3.3.0]octane-3,7-dione; synthesis and crystal structure of 5,7-dihydroxy-4-methoxycarbonyl-3-phenyl-1-indanone. Tetrahedron (1982) 38(1):63-70.
-
(1982)
Tetrahedron
, vol.38
, Issue.1
, pp. 63-70
-
-
Bertz, S.H.1
Rihs, G.2
Woodward, R.B.3
-
36
-
-
21844500176
-
Regioselective aminolysis of diethyl 3-oxoheptanedioate
-
Szychowski J, Wojtasiewicz K: Regioselective aminolysis of diethyl 3-oxoheptanedioate. Polish J Chem (1994) 68:2741-2743.
-
(1994)
Polish J Chem
, vol.68
, pp. 2741-2743
-
-
Szychowski, J.1
Wojtasiewicz, K.2
-
37
-
-
0030845935
-
Practical asymmetric synthesis of (S)-4-ethyl-7,8-dihydro-4-hydroxy-1H- pyrano[3,4-f]indolizine- 3,6,10(4H)-trione, a key intermediate for the synthesis of irinotecan and other camptothecin analogs
-
Henegar KE, Ashford SW, Baughman TA, Sih JC, Gu R-L: Practical asymmetric synthesis of (S)-4-ethyl-7,8-dihydro-4-hydroxy-1H-pyrano[3,4-f]indolizine- 3,6,10(4H)-trione, a key intermediate for the synthesis of irinotecan and other camptothecin analogs. J Org Chem (1997) 62(19):6588-6597.
-
(1997)
J Org Chem
, vol.62
, Issue.19
, pp. 6588-6597
-
-
Henegar, K.E.1
Ashford, S.W.2
Baughman, T.A.3
Sih, J.C.4
Gu, R.-L.5
-
38
-
-
0034597512
-
An efficient enantioselective synthesis of (S)-(-)-acromelobic acid
-
Adamczyk M, Akireddy SR, Reddy RE: An efficient enantioselective synthesis of (S)-(-)-acromelobic acid. Org Lett (2000) 2(22):3421-3423.
-
(2000)
Org Lett
, vol.2
, Issue.22
, pp. 3421-3423
-
-
Adamczyk, M.1
Akireddy, S.R.2
Reddy, R.E.3
-
39
-
-
16844367937
-
Catalysts for Suzuki-Miyaura coupling processes: Scope and studies of the effect of ligand structure
-
Barder TE, Walker SD, Martinelli JR, Buchwald SL: Catalysts for Suzuki-Miyaura coupling processes: Scope and studies of the effect of ligand structure. J Am Chem Soc (2005) 127(13):4685-4696.
-
(2005)
J Am Chem Soc
, vol.127
, Issue.13
, pp. 4685-4696
-
-
Barder, T.E.1
Walker, S.D.2
Martinelli, J.R.3
Buchwald, S.L.4
-
40
-
-
18844421600
-
Simple (imidazol-2-ylidene)-Pd-acetate complexes as effective precatalysts for sterically hindered Suzuki-Miyaura couplings
-
Singh R, Viciu MS, Kramareva N, Navarro O, Nolan SP: Simple (imidazol-2-ylidene)-Pd-acetate complexes as effective precatalysts for sterically hindered Suzuki-Miyaura couplings. Org Lett (2005) 7(9):1829-1832.
-
(2005)
Org Lett
, vol.7
, Issue.9
, pp. 1829-1832
-
-
Singh, R.1
Viciu, M.S.2
Kramareva, N.3
Navarro, O.4
Nolan, S.P.5
-
41
-
-
15944367513
-
General and efficient methodology for the Suzuki-Miyaura reaction in technical grade 2-propanol
-
Navarro O, Oonishi Y, Kelly RA, Stevens ED, Briel O, Nolan SP: General and efficient methodology for the Suzuki-Miyaura reaction in technical grade 2-propanol. J Organometallic Chem (2004) 689(23):3722-3727.
-
(2004)
J Organometallic Chem
, vol.689
, Issue.23
, pp. 3722-3727
-
-
Navarro, O.1
Oonishi, Y.2
Kelly, R.A.3
Stevens, E.D.4
Briel, O.5
Nolan, S.P.6
-
42
-
-
0001388538
-
Suzuki-Miyaura cross-coupling reactions mediated by palladium/imidazolium salt systems
-
Grasa GA, Viciu MS, Huang J, Zhang C, Trudell ML, Nolan SP: Suzuki-Miyaura cross-coupling reactions mediated by palladium/imidazolium salt systems. Organometallics (2002) 21(14):2866-2873.
-
(2002)
Organometallics
, vol.21
, Issue.14
, pp. 2866-2873
-
-
Grasa, G.A.1
Viciu, M.S.2
Huang, J.3
Zhang, C.4
Trudell, M.L.5
Nolan, S.P.6
-
43
-
-
28744436181
-
Efficient synthesis of a trisubstituted 1,6-naphthyridone from acetonedicarboxylate and regioselective Suzuki arylation
-
Chung JYL, Cai C, McWilllams JC, Reamer RA, Dormer PG, Cvetovich RJ: Efficient synthesis of a trisubstituted 1,6-naphthyridone from acetonedicarboxylate and regioselective Suzuki arylation. J Org Chem (2005) 70(25):10342-10347.
-
(2005)
J Org Chem
, vol.70
, Issue.25
, pp. 10342-10347
-
-
Chung, J.Y.L.1
Cai, C.2
McWilllams, J.C.3
Reamer, R.A.4
Dormer, P.G.5
Cvetovich, R.J.6
-
44
-
-
0001725377
-
The abnormal reaction of 2-chloro-4-aminopyridine with nitrous acid
-
Talik T, Plazek E: The abnormal reaction of 2-chloro-4-aminopyridine with nitrous acid. Rocz Chem (1955) 29:1019-1028.
-
(1955)
Rocz Chem
, vol.29
, pp. 1019-1028
-
-
Talik, T.1
Plazek, E.2
-
45
-
-
0008379332
-
A modified method for the preparation of 3-chloro- and 3-bromopyridines
-
Talik T, Talik Z, Ban-Oganowska H: A modified method for the preparation of 3-chloro- and 3-bromopyridines. Synthesis (1974) (4):293-294.
-
(1974)
Synthesis
, Issue.4
, pp. 293-294
-
-
Talik, T.1
Talik, Z.2
Ban-Oganowska, H.3
-
46
-
-
0000620586
-
Use of hydrogen bonds to control molecular aggregation. Behavior of dipyridones and pyridone-pyrimidones designed to form cyclic triplexes
-
Boucher E, Simard M, Wuest JD: Use of hydrogen bonds to control molecular aggregation. Behavior of dipyridones and pyridone-pyrimidones designed to form cyclic triplexes. J Org Chem (1995) 60(5):1408-1412.
-
(1995)
J Org Chem
, vol.60
, Issue.5
, pp. 1408-1412
-
-
Boucher, E.1
Simard, M.2
Wuest, J.D.3
-
47
-
-
0347623383
-
An efficient two-step total synthesis of the quaterpyridine nemertelline
-
Bouillon A, Voisin AS, Robic A, Lancelot J-C, Collot V, Rault S: An efficient two-step total synthesis of the quaterpyridine nemertelline. J Org Chem (2003) 68(26):10178-10180.
-
(2003)
J Org Chem
, vol.68
, Issue.26
, pp. 10178-10180
-
-
Bouillon, A.1
Voisin, A.S.2
Robic, A.3
Lancelot, J.-C.4
Collot, V.5
Rault, S.6
-
48
-
-
33750455833
-
Unique tandem Heck-lactamization naphthyridinone ring formation between acrylanilides and halogenated pyridines
-
Cvetovich RJ, Reamer RA, DiMichele L, Chung JYL, Chilenski J: Unique tandem Heck-lactamization naphthyridinone ring formation between acrylanilides and halogenated pyridines. J Org Chem (2006) 71(22):8610-8613.
-
(2006)
J Org Chem
, vol.71
, Issue.22
, pp. 8610-8613
-
-
Cvetovich, R.J.1
Reamer, R.A.2
DiMichele, L.3
Chung, J.Y.L.4
Chilenski, J.5
-
49
-
-
33750138247
-
Formation of acrylanilides, acrylamides and amides directly from carboxylic acids using thionyl chloride in dimethylacetamide in the absence of bases
-
Cvetovich RJ, DiMichele L: Formation of acrylanilides, acrylamides and amides directly from carboxylic acids using thionyl chloride in dimethylacetamide In the absence of bases. Org Proc Res Dev (2006) 10(5):944-946.
-
(2006)
Org Proc Res Dev
, vol.10
, Issue.5
, pp. 944-946
-
-
Cvetovich, R.J.1
DiMichele, L.2
-
50
-
-
33750435218
-
Synthesis of a naphthyridone p38 MAP kinase inhibitor
-
Chung JYL, Cvetovich RJ, McLaughlin M, Amato J, Tsay F-R, Jensen M, Weissman S, Zewge O: Synthesis of a naphthyridone p38 MAP kinase inhibitor. J Org Chem (2006) 71(22):8602-8609.
-
(2006)
J Org Chem
, vol.71
, Issue.22
, pp. 8602-8609
-
-
Chung, J.Y.L.1
Cvetovich, R.J.2
McLaughlin, M.3
Amato, J.4
Tsay, F.-R.5
Jensen, M.6
Weissman, S.7
Zewge, O.8
-
51
-
-
33750480388
-
Deoxidation of pyridine and quinoline N-oxides with lower alcohols
-
Kurbatova AS, Kurbatov, Yu V, Avezov MR, Otroshchenko OS, Sadykov AS: Deoxidation of pyridine and quinoline N-oxides with lower alcohols. Nauch Tr Samarkand Univ (1963) 167:38-42.
-
(1963)
Nauch Tr Samarkand Univ
, vol.167
, pp. 38-42
-
-
Kurbatova, A.S.1
Kurbatov, Yu.V.2
Avezov, M.R.3
Otroshchenko, O.S.4
Sadykov, A.S.5
-
52
-
-
0008842361
-
The preparation of 4- and 6-chloro-2-chloromethylpyridine
-
Barnes JH, Hartley FR, Jones CEL: The preparation of 4- and 6-chloro-2-chloromethylpyridine. Tetrahedron (1982) 38(22):3277-3280.
-
(1982)
Tetrahedron
, vol.38
, Issue.22
, pp. 3277-3280
-
-
Barnes, J.H.1
Hartley, F.R.2
Jones, C.E.L.3
-
53
-
-
10044239459
-
Acrylate as an efficient dimethylamine trap for the practical synthesis of 1-tert-butyl-4-piperidone via transamination
-
Amato JS, Chung JYL, Cvetovich RJ, Reamer RA, Zhao D, Zhou G, Gong X: Acrylate as an efficient dimethylamine trap for the practical synthesis of 1-tert-butyl-4-piperidone via transamination. Org Process Res Dev (2004) 8(6):939-941.
-
(2004)
Org Process Res Dev
, vol.8
, Issue.6
, pp. 939-941
-
-
Amato, J.S.1
Chung, J.Y.L.2
Cvetovich, R.J.3
Reamer, R.A.4
Zhao, D.5
Zhou, G.6
Gong, X.7
-
54
-
-
14544282838
-
Synthesis of 1-tert-butyl-4-chloropiperidine: Generation of an N-tert-butyl group by the reaction of a dimethyliminium salt with methylmagnesium chloride
-
Amato JS, Chung JY, Cvetovich RJ, Gong X, McLaughlin M, Reamer RA: Synthesis of 1-tert-butyl-4-chloropiperidine: Generation of an N-tert-butyl group by the reaction of a dimethyliminium salt with methylmagnesium chloride. J Org Chem (2005) 70(5):1930-1933.
-
(2005)
J Org Chem
, vol.70
, Issue.5
, pp. 1930-1933
-
-
Amato, J.S.1
Chung, J.Y.2
Cvetovich, R.J.3
Gong, X.4
McLaughlin, M.5
Reamer, R.A.6
-
55
-
-
0141645562
-
Highly functionalized organomagnesium reagents prepared through halogen-metal exchange
-
Knochel P, Dohle W, Gommermann N, Kneisel FF, Kopp F, Korn T, Sapountzis I, Vu VA: Highly functionalized organomagnesium reagents prepared through halogen-metal exchange. Angew Chem Int Ed (2003) 42(36):4302-4320.
-
(2003)
Angew Chem Int Ed
, vol.42
, Issue.36
, pp. 4302-4320
-
-
Knochel, P.1
Dohle, W.2
Gommermann, N.3
Kneisel, F.F.4
Kopp, F.5
Korn, T.6
Sapountzis, I.7
Vu, V.A.8
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