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Results: 1-24 |
Results: 24
A novel radical cyclization of 2-bromoindoles. Synthesis of hexahydropyrrolo[3,4-b]indoles
Authors: Gribble, GW Fraser, HL Badenock, JC
Citation: Gw. Gribble et al., A novel radical cyclization of 2-bromoindoles. Synthesis of hexahydropyrrolo[3,4-b]indoles, CHEM COMMUN, (9), 2001, pp. 805-806
Diels-Alder reactions of 2-and 3-nitroindoles. A simple hydroxycarbazole synthesis
Authors: Kishbaugh, TLS Gribble, GW
Citation: Tls. Kishbaugh et Gw. Gribble, Diels-Alder reactions of 2-and 3-nitroindoles. A simple hydroxycarbazole synthesis, TETRAHEDR L, 42(29), 2001, pp. 4783-4785
Generation and reactions of 2,3-dilithio-N-methylindole. Synthesis of 2,3-disubstituted indoles
Authors: Liu, YB Gribble, GW
Citation: Yb. Liu et Gw. Gribble, Generation and reactions of 2,3-dilithio-N-methylindole. Synthesis of 2,3-disubstituted indoles, TETRAHEDR L, 42(16), 2001, pp. 2949-2951
Ruthenium catalyzed oxidation of haloindoles to isatins
Authors: Gribble, GW Liu, YB
Citation: Gw. Gribble et Yb. Liu, Ruthenium catalyzed oxidation of haloindoles to isatins, ORG PREP PR, 33(6), 2001, pp. 615-619
Kamchatka and Montreal
Authors: Gribble, GW
Citation: Gw. Gribble, Kamchatka and Montreal, AM SCIENT, 89(2), 2001, pp. 107-107
The novel triterpenoid 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid induces apoptosis of human myeloid leukemia cells by a caspase-8-dependent mechanism
Authors: Ito, Y Pandey, P Place, A Sporn, MB Gribble, GW Honda, T Kharbanda, S Kufe, D
Citation: Y. Ito et al., The novel triterpenoid 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid induces apoptosis of human myeloid leukemia cells by a caspase-8-dependent mechanism, CELL GROWTH, 11(5), 2000, pp. 261-267
A synthetic triterpenoid, 2-cyano-3,12-dioxooleana-1,9-dien-28-oic acid (CDDO), is a ligand for the peroxisome proliferator-activated receptor gamma
Authors: Wang, YP Porter, WW Suh, NJ Honda, T Gribble, GW Leesnitzer, LM Plunket, KD Mangelsdorf, DJ Blanchard, SG Willson, TM Sporn, MB
Citation: Yp. Wang et al., A synthetic triterpenoid, 2-cyano-3,12-dioxooleana-1,9-dien-28-oic acid (CDDO), is a ligand for the peroxisome proliferator-activated receptor gamma, MOL ENDOCR, 14(10), 2000, pp. 1550-1556
Recent developments in indole ring synthesis-methodology and applications
Authors: Gribble, GW
Citation: Gw. Gribble, Recent developments in indole ring synthesis-methodology and applications, J CHEM S P1, 7, 2000, pp. 1045-1075
The fused heterocycle 2-benzyl-3-methyl-1-phenyl-4-phenylsulfonyl-2H,4H-pyrrolo[3,4-b]indole
Authors: Simon, WM Trujillo, HA Pelkey, ET Gribble, GW Jasinski, JP
Citation: Wm. Simon et al., The fused heterocycle 2-benzyl-3-methyl-1-phenyl-4-phenylsulfonyl-2H,4H-pyrrolo[3,4-b]indole, ACT CRYST C, 56, 2000, pp. 461-462
A novel class of fused heterocycles, benzo[b]furo[2,3-c]pyrroles
Authors: Trujillo, HA Simon, WM Pelkey, ET Gribble, GW Jasinski, JP
Citation: Ha. Trujillo et al., A novel class of fused heterocycles, benzo[b]furo[2,3-c]pyrroles, ACT CRYST C, 56, 2000, pp. 386-388
Bis-Suzuki reactions of 2,3-dihaloindoles. A convenient synthesis of 2,3-diarylindoles
Authors: Liu, YB Gribble, GW
Citation: Yb. Liu et Gw. Gribble, Bis-Suzuki reactions of 2,3-dihaloindoles. A convenient synthesis of 2,3-diarylindoles, TETRAHEDR L, 41(45), 2000, pp. 8717-8721
Tandem 1,3-dipolar cycloaddition of mesoionic 2,4-diphenyl-1,3-oxathiolium-5-olate with cycloocta-1,5-diene. A new synthesis of the tetracyclo[6.2.0.0(4,)(10).0(5,9)]decane ring system
Authors: Sponholtz, WR Trujillo, HA Gribble, GW
Citation: Wr. Sponholtz et al., Tandem 1,3-dipolar cycloaddition of mesoionic 2,4-diphenyl-1,3-oxathiolium-5-olate with cycloocta-1,5-diene. A new synthesis of the tetracyclo[6.2.0.0(4,)(10).0(5,9)]decane ring system, TETRAHEDR L, 41(11), 2000, pp. 1687-1690
Regioselective 1,3-dipolar cycloaddition reactions of unsymmetrical munchnones (1,3-oxazolium-5-olates) with 2-and 3-nitroindoles. A new synthesis ofpyrrolo[3,4-b]indoles
Authors: Gribble, GW Pelkey, ET Simon, WM Trujillo, HA
Citation: Gw. Gribble et al., Regioselective 1,3-dipolar cycloaddition reactions of unsymmetrical munchnones (1,3-oxazolium-5-olates) with 2-and 3-nitroindoles. A new synthesis ofpyrrolo[3,4-b]indoles, TETRAHEDRON, 56(52), 2000, pp. 10133-10140
Synthesis of beta-boswellic acid analogues with a carboxyl group at C-17 isolated from the bark of Schefflera octophylla
Authors: Bore, L Honda, T Gribble, GW
Citation: L. Bore et al., Synthesis of beta-boswellic acid analogues with a carboxyl group at C-17 isolated from the bark of Schefflera octophylla, J ORG CHEM, 65(19), 2000, pp. 6278-6282
Novel synthetic oleanane and ursane triterpenoids with various enone functionalities in ring A as inhibitors of nitric oxide production in mouse macrophages
Authors: Honda, T Gribble, GW Suh, N Finlay, HJ Rounds, BV Bore, L Favaloro, FG Wang, YP Sporn, MB
Citation: T. Honda et al., Novel synthetic oleanane and ursane triterpenoids with various enone functionalities in ring A as inhibitors of nitric oxide production in mouse macrophages, J MED CHEM, 43(9), 2000, pp. 1866-1877
Synthetic oleanane and ursane triterpenoids with modified rings A and C: Aseries of highly active inhibitors of nitric oxide production in mouse macrophages
Authors: Honda, T Rounds, BV Bore, L Finlay, HJ Favaloro, FG Suh, N Wang, YP Sporn, MB Gribble, GW
Citation: T. Honda et al., Synthetic oleanane and ursane triterpenoids with modified rings A and C: Aseries of highly active inhibitors of nitric oxide production in mouse macrophages, J MED CHEM, 43(22), 2000, pp. 4233-4246
Synthesis and identification of two halogenated bipyrroles present in seabird eggs
Authors: Gribble, GW Blank, DH Jasinski, JP
Citation: Gw. Gribble et al., Synthesis and identification of two halogenated bipyrroles present in seabird eggs, CHEM COMMUN, (21), 1999, pp. 2195-2196
Novel synthetic oleanane triterpenoids: A series of highly active inhibitors of nitric oxide production in mouse macrophages
Authors: Honda, T Rounds, BV Bore, L Favaloro, FG Gribble, GW Suh, N Wang, YP Sporn, MB
Citation: T. Honda et al., Novel synthetic oleanane triterpenoids: A series of highly active inhibitors of nitric oxide production in mouse macrophages, BIOORG MED, 9(24), 1999, pp. 3429-3434
The diversity of naturally occurring organobromine compounds
Authors: Gribble, GW
Citation: Gw. Gribble, The diversity of naturally occurring organobromine compounds, CHEM SOC RE, 28(5), 1999, pp. 335-346
Nucleophilic addition reactions of 2-nitro-1-(phenylsulfonyl)indole. A newsynthesis of 3-substituted-2-nitroindoles
Authors: Pelkey, ET Barden, TC Gribble, GW
Citation: Et. Pelkey et al., Nucleophilic addition reactions of 2-nitro-1-(phenylsulfonyl)indole. A newsynthesis of 3-substituted-2-nitroindoles, TETRAHEDR L, 40(43), 1999, pp. 7615-7619
Intramolecular Diels-Alder reactions of 4H-furo[3,4-b]indoles. New syntheses of benzo[a]carbazoles and benzo[c]carbazoles
Authors: Gribble, GW Silva, RA Saulnier, MG
Citation: Gw. Gribble et al., Intramolecular Diels-Alder reactions of 4H-furo[3,4-b]indoles. New syntheses of benzo[a]carbazoles and benzo[c]carbazoles, SYN COMMUN, 29(4), 1999, pp. 729-747
Synthesis and reactions of N-protected 3-nitroindoles
Authors: Pelkey, ET Gribble, GW
Citation: Et. Pelkey et Gw. Gribble, Synthesis and reactions of N-protected 3-nitroindoles, SYNTHESIS-S, (7), 1999, pp. 1117-1122
A novel synthetic oleanane triterpenoid, 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid, with potent differentiating, antiproliferative, and anti-inflammatory activity
Authors: Suh, NJ Wang, YP Honda, T Gribble, GW Dmitrovsky, E Hickey, WF Maue, RA Place, AE Porter, DM Spinella, MJ Williams, CR Wu, GF Dannenberg, AJ Flanders, KC Letterio, JJ Mangelsdorf, DJ Nathan, CF Nguyen, L Porter, WW Ren, RF Roberts, AB Roche, NS Subbaramaiah, K Sporn, MB
Citation: Nj. Suh et al., A novel synthetic oleanane triterpenoid, 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid, with potent differentiating, antiproliferative, and anti-inflammatory activity, CANCER RES, 59(2), 1999, pp. 336-341
Sodium borohydride in carboxylic acid media: a phenomenal reduction system
Authors: Gribble, GW
Citation: Gw. Gribble, Sodium borohydride in carboxylic acid media: a phenomenal reduction system, CHEM SOC RE, 27(6), 1998, pp. 395-404
Risultati: 1-24 |