-
1
-
-
0036826933
-
Isolation and synthesis of biologically active carbazole alkaloids
-
doi:10.1021/cr020059j
-
Knölker HJ, Reddy KR (2002) Isolation and synthesis of biologically active carbazole alkaloids. Chem Rev 102: 4303-4428. doi:10.1021/cr020059j
-
(2002)
Chem Rev
, vol.102
, pp. 4303-4428
-
-
Knölker, H.J.1
Reddy, K.R.2
-
2
-
-
44949230366
-
Chemistry and biology of carbazole alkaloids
-
Knölker HJ, Reddy KR (2008) Chemistry and biology of carbazole alkaloids. Alkaloids Chem Biol 65:1-410
-
(2008)
Alkaloids Chem Biol
, vol.65
, pp. 1-410
-
-
Knölker, H.J.1
Reddy, K.R.2
-
4
-
-
67949083651
-
Antifungal carbazoles
-
Thevissen K, Marchand A, Chaltin P, Meert EMK, Cammue BPA (2009) Antifungal carbazoles. Curr Med Chem 16: 2205-2211
-
(2009)
Curr Med Chem
, vol.16
, pp. 2205-2211
-
-
Thevissen, K.1
Marchand, A.2
Chaltin, P.3
Meert, E.M.K.4
Cammue, B.P.A.5
-
5
-
-
0021816422
-
Isolation and structure of rebeccamycin - A new antitumor antibiotic from Nocardia aerocoligenes
-
DOI 10.1016/S0040-4039(00)89280-1
-
Nettleton DE, Doyle TW, Krishnan B, Matsumoto GK, Clardy J (1985) Isolation and structure of rebeccamycin-a new antitumor antibiotic from nocardia aerocoligenes. Tetrahedron Lett 26: 4011-4014 (Pubitemid 15024794)
-
(1985)
Tetrahedron Letters
, vol.26
, Issue.34
, pp. 4011-4014
-
-
Nettleton, D.E.1
Doyle, T.W.2
Krishnan, B.3
-
6
-
-
0023178261
-
Production and biological activity of rebeccamycin, a novel antitumor agent
-
Bush JA, Long BH, Catino JJ, Bradner WT, Tomita K (1987) Production and biological activity of rebeccamycin, a novel antitumor agent. J Antibiot 40:668-678 (Pubitemid 17072164)
-
(1987)
Journal of Antibiotics
, vol.40
, Issue.5
, pp. 668-678
-
-
Bush, J.A.1
Long, B.H.2
Catino, J.J.3
Bradner, W.T.4
-
7
-
-
0030944043
-
DNA cleavage by topoisomerase I in the presence of indolocarbazole derivatives of rebeccamycin
-
DOI 10.1021/bi9624898
-
Bailly C, Riou JF, Colson P, Houssier C, Rodrigues-Pereira E, Prudhomme M (1997) DNA cleavage by topoisomerase I in the presence of indolocarbazole derivatives of rebeccamycin. Biochemistry 36: 3917-3929. doi:10.1021/bi9624898 (Pubitemid 27154713)
-
(1997)
Biochemistry
, vol.36
, Issue.13
, pp. 3917-3929
-
-
Bailly, C.1
Riou, J.-F.2
Colson, P.3
Houssier, C.4
Rodrigues-Pereira, E.5
Prudhomme, M.6
-
8
-
-
0033587125
-
Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives
-
doi:10.1021/jm980702n
-
Moreau P, Anizon F, Sancelme M, Prudhomme M, Severe D, Riou JF, Goosens JF, Henichart JP, Bailly C, Labourier E, Tazzi J, Fabbro D, Meyer T, Aubertin AM (1999) Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives. J Med Chem 42: 1816-1822. doi:10.1021/jm980702n
-
(1999)
J Med Chem
, vol.42
, pp. 1816-1822
-
-
Moreau, P.1
Anizon, F.2
Sancelme, M.3
Prudhomme, M.4
Severe, D.5
Riou, J.F.6
Goosens, J.F.7
Henichart, J.P.8
Bailly, C.9
Labourier, E.10
Tazzi, J.11
Fabbro, D.12
Meyer, T.13
Aubertin, A.M.14
-
9
-
-
9844260513
-
Syntheses and biological activities (Topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group
-
doi:10.1021/jm9702084
-
Anizon F, Belin L, Moreau P, Sancelme M, Voldoire A, Prudhomme M, Ollier M, Severe D, Riou JF, Bailly C, FabbroD,Meyer T (1997) Syntheses and biological activities (Topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. J Med Chem 40: 3456-3465. doi:10.1021/jm9702084
-
(1997)
J Med Chem
, vol.40
, pp. 3456-3465
-
-
Anizon, F.1
Belin, L.2
Moreau, P.3
Sancelme, M.4
Voldoire, A.5
Prudhomme, M.6
Ollier, M.7
Severe, D.8
Riou, J.F.9
Bailly, C.10
Fabbro, D.11
Meyer, T.12
-
10
-
-
15144351325
-
Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle
-
DOI 10.1021/jm970843+
-
Moreau P, Anizon F, Sancelme M, Prudhomme M, Bailly C, Carrasco C, Ollier M, Severe D, Riou JF, Fabbro D,Meyer T, Aubertin AM (1998) Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin,modified at the imide heterocycle. J Med Chem 41: 1631-1640. doi:10.1021/jm970843+ (Pubitemid 28221956)
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, Issue.10
, pp. 1631-1640
-
-
Moreau, P.1
Anizon, F.2
Sancelme, M.3
Prudhomme, M.4
Bailly, C.5
Carrasco, C.6
Ollier, M.7
Severe, D.8
Riou, J.-F.9
Fabbro, D.10
Meyer, T.11
Aubertin, A.-M.12
-
11
-
-
0033597875
-
Conformational control in the rebeccamycin class of indolocarbazole glycosides
-
doi:10.1021/jo990296v
-
GilbertEJ, Chisholm JD,VanVranken DL. (1999) Conformational control in the rebeccamycin class of indolocarbazole glycosides. J Org Chem 64: 5670-5676. doi:10.1021/jo990296v
-
(1999)
J Org Chem
, vol.64
, pp. 5670-5676
-
-
Gilbert, E.J.1
Chisholm, J.D.2
VanVranken, D.L.3
-
12
-
-
0017395981
-
A new alkaloid AM 2282 of Streptomyces origin taxonomy, fermentation, isolation and preliminary characterization
-
Omura S, Iwai Y, Hirano A, Nakagawa A, Awaya J, Tsuchya H, Takahashi Y, Masuma R (1977) A new alkaloid AM-282 of streptomyces origin taxonomy, fermentation, isolation and preliminary characterization. J Antibiot 30:275-282 (Pubitemid 8119845)
-
(1977)
Journal of Antibiotics
, vol.30
, Issue.4
, pp. 275-282
-
-
Omura, S.1
Iwai, Y.2
Hirano, A.3
-
13
-
-
0024394417
-
Staurosporine, K-252 and UCN-01: Potent but nonspecific inhibitors of protein kinases
-
Ruegg UT, Burgess GM (1989) Staurosporine, K-252 and UCN-01: potent but nonspecific inhibitors of protein kinases. Trends Pharmacol Sci 10:218-220
-
(1989)
Trends Pharmacol Sci
, vol.10
, pp. 218-220
-
-
Ruegg, U.T.1
Burgess, G.M.2
-
14
-
-
6444232494
-
Biological targets of antitumor indolocarbazoles bearing a sugarmoiety
-
Prudhomme M (2004) Biological targets of antitumor indolocarbazoles bearing a sugarmoiety. Curr MedChemAnticancer Agents 4:509-521
-
(2004)
Curr MedChemAnticancer Agents
, vol.4
, pp. 509-521
-
-
Prudhomme, M.1
-
15
-
-
0034040974
-
UCN-01 (7-hydroxystaurosporine) and other indolocarbazole compounds: A new generation of anti-cancer agents for the new century?
-
Akinaga S, Sugiyama K, Akiyama T (2000) UCN-01 (7-hydroxystaurosporine) and other indolocarbazole compounds: a new generation of anti-cancer agents for the new century?. Anticancer Drug Des 15:43-52
-
(2000)
Anticancer Drug des
, vol.15
, pp. 43-52
-
-
Akinaga, S.1
Sugiyama, K.2
Akiyama, T.3
-
16
-
-
31544452150
-
Phase I trial of UCN-01 in combination with topotecan in patients with advanced solid cancers: A Princess Margaret Hospital Phase II Consortium study
-
DOI 10.1093/annonc/mdj076
-
Hotte SJ, Oza A, Winquist EW, Moore M, Chen EX, Brown S, Pond GR, Dancey JE, Hirte HW (2006) Phase I trial of UCN-01 in combination with topotecan in patients with advanced solid cancers: a PrincessMargaret Hospital Phase II Consortium study. Ann Oncol 17: 334-340. doi:10.1093/annonc/mdj076 (Pubitemid 43160126)
-
(2006)
Annals of Oncology
, vol.17
, Issue.2
, pp. 334-340
-
-
Hotte, S.J.1
Oza, A.2
Winquist, E.W.3
Moore, M.4
Chen, E.X.5
Brown, S.6
Pond, G.R.7
Dancey, J.E.8
Hirte, H.W.9
-
17
-
-
7444245571
-
2 DNA damage checkpoint inhibitor isogranulatimide
-
2 DNA damage checkpoint inhibitor isogranulatimide. Mol Cancer Ther 3:1221-1227
-
(2004)
Mol Cancer Ther
, vol.3
, pp. 1221-1227
-
-
Jiang, X.1
Zhao, B.2
Britton, R.3
Lim, L.Y.4
Leong, D.5
Sanghera, J.S.6
Zhou, B.B.S.7
Piers, E.8
Andersen, R.J.9
Roberge, M.10
-
18
-
-
34648816236
-
Synthesis and biological activities of new checkpoint kinase 1 inhibitors structurally related to granulatimide
-
DOI 10.1021/jm070664k
-
Conchon E, Anizon F, Aboab B, Prudhomme M (2007) Synthesis and biological activities of new checkpoint kinase 1 inhibitors structurally related to granulatimide. J Med Chem 50: 4669-4680. doi:10.1021/jm070664k (Pubitemid 47463241)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.19
, pp. 4669-4680
-
-
Conchon, E.1
Anizon, F.2
Aboab, B.3
Prudhomme, M.4
-
19
-
-
42149187861
-
Synthesis, checkpoint kinase 1 inhibitory properties and in vitro antiproliferative activities of new pyrrolocarbazoles
-
DOI 10.1016/j.bmc.2008.02.061, PII S0968089608001818
-
Conchon E, Anizon F, Aboab B, Golsteyn RM, Leonce S, Pfeiffer B, PrudhommeM (2008) Synthesis, checkpoint kinase 1 inhibitory properties and in vitro antiproliferative activities of new pyrrolocarbazoles. BioorgMedChem16:4419-4430. doi:10.1016/j.bmc.2008.02.061 (Pubitemid 351539037)
-
(2008)
Bioorganic and Medicinal Chemistry
, vol.16
, Issue.8
, pp. 4419-4430
-
-
Conchon, E.1
Anizon, F.2
Aboab, B.3
Golsteyn, R.M.4
Leonce, S.5
Pfeiffer, B.6
Prudhomme, M.7
-
20
-
-
33845336481
-
Bis-imide granulatimide analogues as potent Checkpoint 1 kinase inhibitors
-
DOI 10.1016/j.ejphar.2006.10.022, PII S0014299906011484
-
Henon H, Messaoudi S, Anizon F, Aboab B, Kucharczyk N, Leonce S, Golsteyn RM, Pfeiffer B, Prudhomme M (2007) Bis-imide granulatimide analogues as potent checkpoint 1 kinase inhibitors. Eur J Pharmcol 554: 106-112. doi:10.1016/j.ejphar.2006.10.022 (Pubitemid 44879419)
-
(2007)
European Journal of Pharmacology
, vol.554
, Issue.2-3
, pp. 106-112
-
-
Henon, H.1
Messaoudi, S.2
Anizon, F.3
Aboab, B.4
Kucharczyk, N.5
Leonce, S.6
Golsteyn, R.M.7
Pfeiffer, B.8
Prudhomme, M.9
-
21
-
-
33646023982
-
Synthesis and biological evaluation of new dipyrrolo[3,4-a:3,4-c] carbazole-1,3,4,6-tetraones, substituted with various saturated and unsaturated side chains via palladium catalyzed cross-coupling reactions
-
doi:10.1016/j.bmc.2006.01.030
-
Henon H, Anizon F, Golsteyn RM, Leonce S, Hofmann R, Pfeiffer B, Prudhomme M (2006) Synthesis and biological evaluation of new dipyrrolo[3,4-a:3,4-c]carbazole-1,3,4,6-tetraones, substituted with various saturated and unsaturated side chains via palladium catalyzed cross-coupling reactions. Bioorg Med Chem 14: 3825-3834. doi:10.1016/j.bmc.2006.01.030
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 3825-3834
-
-
Henon, H.1
Anizon, F.2
Golsteyn, R.M.3
Leonce, S.4
Hofmann, R.5
Pfeiffer, B.6
Prudhomme, M.7
-
22
-
-
12444304196
-
Aryl[a]pyrrolo[3,4-c]carbazoles as selective Cyclin D1-CDK4 inhibitors
-
DOI 10.1016/S0960-894X(03)00791-1
-
Sanchez-Martinez C, Shih C, Faul MM, Zhu G, Paal M, Somoza C, Li T, Kumrich CA, Winneroski LL, Xun Z (2003) Aryl[a]pyrrolo[3,4-c]carbazoles as selective cyclin D1-CDK4 inhibitors. Bioorg Med Chem Lett 13: 3835-3839. doi:10.1016/j.bmcl.2004.04.088 (Pubitemid 37206519)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.21
, pp. 3835-3839
-
-
Sanchez-Martinez, C.1
Shih, C.2
Faul, M.M.3
Zhu, G.4
Paal, M.5
Somoza, C.6
Li, T.7
Kumrich, C.A.8
Winneroski, L.L.9
Xun, Z.10
Brooks, H.B.11
Patel, B.K.R.12
Schultz, R.M.13
DeHahn, T.B.14
Spencer, C.D.15
Watkins, S.A.16
Considine, E.17
Dempsey, J.A.18
Ogg, C.A.19
Campbell, R.M.20
Anderson, B.A.21
Wagner, J.22
more..
-
23
-
-
0033585089
-
Calothrixins A and B, novel pentacyclic metabolites from Calothrix cyanobacteria with potent activity against malaria parasites and human cancer cells
-
DOI 10.1016/S0040-4020(99)00833-9, PII S0040402099008339
-
Richards RW, Rothschild JM, Willis AC, de Chazal NM, Kirk K, Saliba KJ, Smith GD (1999) Calothrixins A and B, novel pentacyclic metabolites from calothrix cyanobacteria with potent activity against malaria parasites and human cancer cells. Tetrahedron 55:13513-13520 (Pubitemid 29521193)
-
(1999)
Tetrahedron
, vol.55
, Issue.47
, pp. 13513-13520
-
-
Rickards, R.W.1
Rothschild, J.M.2
Willis, A.C.3
De Chazal, N.M.4
Kirk, J.5
Kirk, K.6
Saliba, K.J.7
Smith, G.D.8
-
24
-
-
33750466576
-
Concise and efficient synthesis of calothrixin B
-
DOI 10.1021/jo061270o
-
Sissouma D,Maingot L, Collet S, Guingant A (2006) Concise and efficient synthesis of calothrixin B. J Org Chem 71: 8384-8389. doi:10.1021/jo061270o (Pubitemid 44656026)
-
(2006)
Journal of Organic Chemistry
, vol.71
, Issue.22
, pp. 8384-8389
-
-
Sissouma, D.1
Maingot, L.2
Collet, S.3
Guingant, A.4
-
25
-
-
33751335837
-
Indolocarbazole natural products: Occurrence, biosynthesis, and biological activity
-
doi:10.1039/b601930g
-
Sanchez C, Mendez C, Salas JA (2006) Indolocarbazole natural products: occurrence, biosynthesis, and biological activity. Nat Prod Rep 23: 1007-1045. doi:10.1039/b601930g
-
(2006)
Nat Prod Rep
, vol.23
, pp. 1007-1045
-
-
Sanchez, C.1
Mendez, C.2
Salas, J.A.3
-
26
-
-
52749086350
-
Pyrrolocarbazoles as checkpoint 1 kinase inhibitors
-
Henon H, Conchon E, Hugon B, Messaoudi S, Golsteyn RM, Prudhomme M (2008) Pyrrolocarbazoles as checkpoint 1 kinase inhibitors. Anti Cancer Agents Med Chem 8:577-597
-
(2008)
Anti Cancer Agents Med Chem
, vol.8
, pp. 577-597
-
-
Henon, H.1
Conchon, E.2
Hugon, B.3
Messaoudi, S.4
Golsteyn, R.M.5
Prudhomme, M.6
-
27
-
-
33750003936
-
Synthesis, in vitro antiproliferative activities, and Chk1 inhibitory properties of dipyrrolo[3,4-a:3,4-c]carbazole-triones
-
DOI 10.1016/j.tet.2006.09.027, PII S0040402006014918
-
Conchon E, Anizon F, Golsteyn RM, Leonce S, Pfeiffer B, Prudhomme M (2006) Synthesis, in vitro antiproliferative activities, and Chk1 inhibitory properties of dipyrrolo[3,4-a:3,4-c]carbazoletriones. Tetrahedron 62: 11136-11144. doi:10.1016/j.tet.2006.09.027 (Pubitemid 44573336)
-
(2006)
Tetrahedron
, vol.62
, Issue.48
, pp. 11136-11144
-
-
Conchon, E.1
Anizon, F.2
Golsteyn, R.M.3
Leonce, S.4
Pfeiffer, B.5
Prudhomme, M.6
-
28
-
-
33644500795
-
Expedited synthesis of substituted dipyrrolo[3,4-a:3,4-c]carbazole-1,3,4, 6-tetraones structurally related to granulatimide
-
Henon H, Anizon F, Kucharczyk N, Loynel A, Casara P, Pfeiffer B, PrudhommeM (2006) Expedited synthesis of substituted dipyrrolo[3,4-a:3,4-c] carbazole-1,3,4,6-tetraones structurally related to granulatimide. Synthesis 4:711-715
-
(2006)
Synthesis
, vol.4
, pp. 711-715
-
-
Henon, H.1
Anizon, F.2
Kucharczyk, N.3
Loynel, A.4
Casara, P.5
Pfeiffer, B.6
Prudhomme, M.7
-
29
-
-
29744470612
-
Synthesis of dipyrrolo[3,4-a:3,4-c]carbazole-1,3,4,6-tetraones bearing a sugar moiety
-
doi:10.1016/j.tet.2005.10.077
-
Henon H, Anizon F, Pfeiffer B, Prudhomme M (2006) Synthesis of dipyrrolo[3,4-a:3,4-c]carbazole-1,3,4,6-tetraones bearing a sugar moiety. Tetrahedron 62: 1116-1123. doi:10.1016/j.tet.2005.10.077
-
(2006)
Tetrahedron
, vol.62
, pp. 1116-1123
-
-
Henon, H.1
Anizon, F.2
Pfeiffer, B.3
Prudhomme, M.4
-
30
-
-
19044362490
-
Synthesis of granulatimide bis-imide analogues
-
DOI 10.1016/j.tet.2005.03.101, PII S0040402005005867
-
Henon H, Messaoudi S, Hugon B, Anizon F, Pfeiffer B, Prudhomme M (2005) Synthesis of granulatimide bis-imide analogues. Tetrahedron 61: 5599-5614. doi:10.1016/j.tet.2005.03.101 (Pubitemid 40712283)
-
(2005)
Tetrahedron
, vol.61
, Issue.23
, pp. 5599-5614
-
-
Henon, H.1
Messaoudi, S.2
Hugon, B.3
Anizon, F.4
Pfeiffer, B.5
Prudhomme, M.6
-
31
-
-
0842348235
-
1-Phthalimido-4-(3-indolyl)-2-siloxy-1,3-butadienes: Synthesis and Diels-Alder reactivity
-
DOI 10.1016/j.tetlet.2003.12.118
-
Caballero E, Alonso D, Pelaez R, Alvarez C, Puebla P, Sanz F, MedardeM,TomeF (2004) 1-Phthalimido-4-(3-indolyl)-2-siloxy-1,3-butadienes: synthesis and Diels-Alder reactivity. Tetrahedron Lett 45:1631-1634. doi:10.1016/j.tetlet.2003.12.118 (Pubitemid 38169289)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.8
, pp. 1631-1634
-
-
Caballero, E.1
Alonso, D.2
Pelaez, R.3
Alvarez, C.4
Puebla, P.5
Sanz, F.6
Medarde, M.7
Tome, F.8
-
32
-
-
0041520600
-
Synthesis of granulatimide positional analogues
-
DOI 10.1248/cpb.51.209
-
Yoshida T, Nishiyachi M, Nakashima N, Murase M, Kotani E (2003) Synthesis of granulatimide positional analogues. Chem Pharm Bull 51: 209-214. doi:10.1248/cpb.51.209 (Pubitemid 41701997)
-
(2003)
Chemical and Pharmaceutical Bulletin
, vol.51
, Issue.2
, pp. 209-214
-
-
Yoshida, T.1
Nishiyachi, M.2
Nakashima, N.3
Murase, M.4
Kotani, E.5
-
33
-
-
0242669219
-
Synthesis of granulatimide analogues bearing a maleimide instead of an imidazole heterocycle
-
DOI 10.1016/S0040-4039(03)00823-2
-
Hugon B, Pfeiffer B, Renard P, PrudhommeM (2003) Synthesis of granulatimide analogues bearing a maleimide instead of an imidazole heterocycle. Tetrahedron Lett 44: 3935-3937. doi:10.1016/S0040-4039(03)00823-2 (Pubitemid 36513808)
-
(2003)
Tetrahedron Letters
, vol.44
, Issue.20
, pp. 3935-3937
-
-
Hugon, B.1
Pfeiffer, B.2
Renard, P.3
Prudhomme, M.4
-
34
-
-
0036596485
-
New synthetic route to granulatimide and its structural analogues
-
DOI 10.1248/cpb.50.872
-
Yoshida T, Nishiyachi M, Nakashima N, Murase M, Kotani E (2002) New synthetic route to granulatimide and its structural analogues. Chem Pharm Bull 50: 872-876. doi:10.1248/cpb.50.872 (Pubitemid 41694917)
-
(2002)
Chemical and Pharmaceutical Bulletin
, vol.50
, Issue.6
, pp. 872-876
-
-
Yoshida, T.1
Nishiyachi, M.2
Nakashima, N.3
Murase, M.4
Kotani, E.5
-
35
-
-
70349119077
-
Synthesis study on marmycin a: Preparation of the C3′-desmethyl analogues
-
doi:10.1021/jo9011078
-
Ding CY, Tu SH, Li FY, Wang YX, Yao QZ, Hu WX, Xie H, Meng LH, Zhang A (2009) Synthesis study on marmycin a: preparation of the C3′-desmethyl analogues. JOrg Chem 74: 6111-6119. doi:10.1021/jo9011078
-
(2009)
JOrg Chem
, vol.74
, pp. 6111-6119
-
-
Ding, C.Y.1
Tu, S.H.2
Li, F.Y.3
Wang, Y.X.4
Yao, Q.Z.5
Hu, W.X.6
Xie, H.7
Meng, L.H.8
Zhang, A.9
-
36
-
-
0002176149
-
Silver(I)-catalyzed oxidative decarboxylation of acids by peroxydisulfate. Role of silver (II)
-
doi:10.1021/ja00709a039
-
Anderson JM, Kochi JK (1970) Silver(I)-catalyzed oxidative decarboxylation of acids by peroxydisulfate. Role of silver (II). J Am Chem Soc 92: 1651-1659. doi:10.1021/ja00709a039
-
(1970)
J Am Chem Soc
, vol.92
, pp. 1651-1659
-
-
Anderson, J.M.1
Kochi, J.K.2
-
37
-
-
84959947882
-
Novel applications of free-radical reactions in preparative organic chemistry
-
Minisci F (1973) Novel applications of free-radical reactions in preparative organic chemistry. Synthesis 5:1-24
-
(1973)
Synthesis
, vol.5
, pp. 1-24
-
-
Minisci, F.1
-
38
-
-
0345359241
-
Use of N-protected amino acids in the minisci radical alkylation
-
doi:10.1021/ol801736h
-
Cowden CJ (2003) Use of N-protected amino acids in the minisci radical alkylation. Org Lett 5: 4497-4499. doi:10.1021/ol801736h
-
(2003)
Org Lett
, vol.5
, pp. 4497-4499
-
-
Cowden, C.J.1
-
39
-
-
77950364806
-
One-pot three-step synthesis of naphtho[2,3-a]carbazole-5,13-diones using tandem radical alkylation-cyclization-aromatization reaction sequence
-
adsc.200900789, doi:10.1002/adsc.200
-
Ding CY, Tu SH, Yao QZ, Li FL, Wang YX, Hu WX, Zhang A (2009) One-pot three-step synthesis of naphtho[2,3-a]carbazole-5,13-diones using tandem radical alkylation-cyclization-aromatization reaction sequence. Adv Synth Catal (adsc.200900789, doi:10.1002/adsc.200)
-
(2009)
Adv Synth Catal
-
-
Ding, C.Y.1
Tu, S.H.2
Yao, Q.Z.3
Li, F.L.4
Wang, Y.X.5
Hu, W.X.6
Zhang, A.7
-
40
-
-
0001952635
-
[α]-anellated carbazoles with antitumor activity: Synthesis and cytotoxicity
-
Rogge M, Fischer G, Pindur U, Schollmeyer D (1996) [α]-anellated carbazoles with antitumor activity: synthesis and cytotoxicity. Monatsh Chem 127:97-102
-
(1996)
Monatsh Chem
, vol.127
, pp. 97-102
-
-
Rogge, M.1
Fischer, G.2
Pindur, U.3
Schollmeyer, D.4
-
41
-
-
0033784332
-
Functionalized and [a]-anellated carbazoles as potential B-DNA ligands: Experimental studies of DNA binding and molecular modelling of intercalation complexes
-
Pindur U, Marotto A, Schulze E, Fischer G (2000) Functionalized and [a]-anellated carbazoles as potential B-DNA ligands: experimental studies of DNA binding and molecular modelling of intercalation complexes. Pharmazie 55:717-732
-
(2000)
Pharmazie
, vol.55
, pp. 717-732
-
-
Pindur, U.1
Marotto, A.2
Schulze, E.3
Fischer, G.4
-
42
-
-
84985720970
-
Anewmethod for the conversion of halophenols and halonaphthols to quinnones
-
Perumal PT, BhattMV (1979) Anewmethod for the conversion of halophenols and halonaphthols to quinnones. Synthesis 3:205-206
-
(1979)
Synthesis
, vol.3
, pp. 205-206
-
-
Perumal, P.T.1
Bhatt, M.V.2
-
43
-
-
43849106837
-
Intramolecular direct arylation in the synthesis of fluorinated carbazoles
-
doi:10.1016/j.tet.2008.01.143
-
Bedford RB, Betham M, Charmant JPH, Weeks AL (2008) Intramolecular direct arylation in the synthesis of fluorinated carbazoles. Tetrahedron 64: 6038-6050. doi:10.1016/j.tet.2008.01.143
-
(2008)
Tetrahedron
, vol.64
, pp. 6038-6050
-
-
Bedford, R.B.1
Betham, M.2
Charmant, J.P.H.3
Weeks, A.L.4
-
44
-
-
41149150442
-
Synthesis of a small library of 2-phenoxy-1,4-naphthoquinone and 2-phenoxy-1,4-anthraquinone derivatives bearing anti-trypanosomal and anti-leishmanial activity
-
doi:10.1016/j.bmcl.2008.03.009
-
Bolognesi ML, Lizzi F, Perozzo R, Brunc R, Cavallia A (2008) Synthesis of a small library of 2-phenoxy-1,4-naphthoquinone and 2-phenoxy-1,4-anthraquinone derivatives bearing anti-trypanosomal and anti-leishmanial activity.BioorgMed Chem Lett 18: 2272-2276. doi:10.1016/j.bmcl.2008.03.009
-
(2008)
BioorgMed Chem Lett
, vol.18
, pp. 2272-2276
-
-
Bolognesi, M.L.1
Lizzi, F.2
Perozzo, R.3
Brunc, R.4
Cavallia, A.5
-
45
-
-
7044222425
-
Studies toward the total synthesis of angelmicin B (hibarimicin B): Synthesis of a model CD-D′ arylnaphthoquinone
-
doi:10.1021/ol0613822
-
Narayan S, RoushWR (2004) Studies toward the total synthesis of angelmicin B (hibarimicin B): synthesis of a model CD-D′ arylnaphthoquinone. Org Lett 6: 3789-3792. doi:10.1021/ol0613822
-
(2004)
Org Lett
, vol.6
, pp. 3789-3792
-
-
Narayan, S.1
Roush, W.R.2
-
46
-
-
0032818056
-
Oxygen as oxidant in palladium-catalyzed inter- And intramolecular coupling reactions
-
Hagelin H, D Oslob J, Akermark B (1999) Oxygen as oxidant in palladium-catalyzed inter- and intramolecular coupling reactions. Chem Eur J 5: 2413-2416. doi:10.1002/(SICI)1521-3765(19990802)5:8〈2413 (Pubitemid 129502678)
-
(1999)
Chemistry - A European Journal
, vol.5
, Issue.8
, pp. 2413-2416
-
-
Hagelin, H.1
Oslob, J.D.2
Akermark, B.3
-
47
-
-
35048815950
-
Elements of regiocontrol in palladium-catalyzed oxidative arene cross-coupling
-
DOI 10.1021/ja0745862
-
Stuart DR, Villemure E, Fagnou K (2007) Elements of regiocontrol in palladium-catalyzed oxidative arene cross-coupling. J Am Chem Soc 129: 12072-12073. doi:10.1021/ja0745862 (Pubitemid 47556825)
-
(2007)
Journal of the American Chemical Society
, vol.129
, Issue.40
, pp. 12072-12073
-
-
Stuart, D.R.1
Villemure, E.2
Fagnou, K.3
-
48
-
-
37249011908
-
Total synthesis of the proposed structure of the anthrapyran metabolite δ-indomycinone
-
DOI 10.1002/chem.200700823
-
Tietze LF, Singidi RR, Gericke KM (2007) Total synthesis of the proposed structure of the anthrapyran metabolite δ-indomycinone. Chem Eur J 13: 9939-9947. doi:10.1002/chem.200700823 (Pubitemid 350279701)
-
(2007)
Chemistry - A European Journal
, vol.13
, Issue.35
, pp. 9939-9947
-
-
Tietze, L.F.1
Singidi, R.R.2
Gericke, K.M.3
|