-
1
-
-
0030002598
-
Dispacamides, anti-histamine alkaloids from Caribbean Agelas sponges
-
DOI 10.1016/0040-4039(96)00629-6
-
Cafieri F, Fattorusso E, Mangoni A, Taglialatela Scafati O (1996) Dispacamides anti-histamine alkaloids from Caribbean agelas sponges. Tetrahedron Lett 3:3587-3590. doi:10.1016/0040-4039 (96) 00629-6 (Pubitemid 26164734)
-
(1996)
Tetrahedron Letters
, vol.37
, Issue.20
, pp. 3587-3590
-
-
Cafieri, F.1
Fattorusso, E.2
Mangoni, A.3
Taglialatela-Scafati, O.4
-
2
-
-
0022478418
-
A novel antagonist of serotonergic receptors, hymenidin, isolated from the Okinawan marine sponge Hymeniacidon sp
-
Kobayashi J, Ohizumi Y, Nakamura H, Hirata Y (1986) A novel antagonist of serotonergic receptors, hymenidin, isolated from the Okinawan marine Sponge Hymeniacidon sp. Experientia 42:1176-1177. doi:10.1007/BF01941300 (Pubitemid 16004276)
-
(1986)
Experientia
, vol.42
, Issue.10
, pp. 1176-1177
-
-
Kobayashi, J.1
Ohizumi, Y.2
Nakamura, H.3
Hirata, Y.4
-
3
-
-
0000439301
-
2-Amino imidazole alkaloids from the marine sponge leucetta chagosensis
-
doi:10.1016/S0040-4020 01 80079-X
-
Carmely S, Ilan M, Kashman Y (1989) 2-Amino imidazole alkaloids from the marine sponge leucetta chagosensis. Tetrahedron 45:2193-2200. doi:10.1016/S0040-4020 (01) 80079-X
-
(1989)
Tetrahedron
, vol.45
, pp. 2193-2200
-
-
Carmely, S.1
Ilan, M.2
Kashman, Y.3
-
4
-
-
0024442047
-
Première synthèse totale de la girolline
-
doi:10. 1016/S0040-4020 01 89141-9
-
Bedoya Zurita M, Ahond A, Poupat C, Potier P (1989) Première synthèse totale de la girolline. Tetrahedron 45:6713-6720. doi:10. 1016/S0040-4020 (01) 89141-9
-
(1989)
Tetrahedron
, vol.45
, pp. 6713-6720
-
-
Zurita, M.B.1
Ahond, A.2
Poupat, C.3
Potier, P.4
-
5
-
-
0036691567
-
New and biologically active imidazole alkaloids from two sponges of the genus Leucetta
-
DOI 10.1021/np020050c
-
Gross H, Kehraus S, Koenig GM, Woerheide G, Wright AD (2002) New and biologically active imidazole alkaloids from two sponges of the genus leucetta. J Nat Prod 65:1190-1193. doi:10. 1021/np020050c (Pubitemid 34976504)
-
(2002)
Journal of Natural Products
, vol.65
, Issue.8
, pp. 1190-1193
-
-
Gross, H.1
Kehraus, S.2
Konig, G.M.3
Woerheide, G.4
Wright, A.D.5
-
6
-
-
2542583160
-
New imidazole alkaloids from the Indonesian sponge Leucetta chagosensis
-
DOI 10.1021/np0305223
-
Hassan W, Edrada R, Ebel R, Wray V, Berg A, Van Soest R, Wiryowidagdo S, Proksch P (2004) New imidazole alkaloids from the indonesian sponge leucetta chagosensis. J Nat Prod 67:817-822. doi:10.1021/np0305223 (Pubitemid 38702738)
-
(2004)
Journal of Natural Products
, vol.67
, Issue.5
, pp. 817-822
-
-
Hassan, W.1
Edrada, R.2
Ebel, R.3
Wray, V.4
Berg, A.5
Van Soest, R.6
Wiryowidagdo, S.7
Proksch, P.8
-
7
-
-
0032563853
-
Naamidine A is an antagonist of the epidermal growth factor receptor and an in vivo active antitumor agent
-
DOI 10.1021/jm980294n
-
Copp BR, Fairchild CR, Cornell L, Casazza AM, Robinson S, Ireland CM (1998) Naamidine A is an antagonist of the epidermal growth factor receptor and an in vivo active antitumor agent. J Med Chem 41:3909-3911. doi:10.1021/ jm980294n (Pubitemid 28447318)
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, Issue.20
, pp. 3909-3911
-
-
Copp, B.R.1
Fairchild, C.R.2
Cornell, L.3
Casazza, A.M.4
Robinson, S.5
Ireland, C.M.6
-
8
-
-
0026589407
-
Mode of action of the antitumor compound girodazole
-
doi:10.1016/0006-2952 92 90701-J
-
Colson G, Raboult L, Lavelle F, Zeaial A (1992) Mode of action of the antitumor compound girodazole. Biochem Pharmacol 43:1717-1723. doi:10.1016/0006-2952 (92) 90701-J
-
(1992)
Biochem Pharmacol
, vol.43
, pp. 1717-1723
-
-
Colson, G.1
Raboult, L.2
Lavelle, F.3
Zeaial, A.4
-
9
-
-
0034642555
-
3
-
DOI 10.1021/jm9900321
-
Pitts WJ, Wityak J, Smallheer JM, Tobin AE, Jetter JW, Buynitsky JS, Harlow PP, Solomon KA, Corjay MH, Mousa SA, Wexler R, Jadhav PK (2000) Isoxazolines as potent antagonists of the integrin αvβ3. J Med Chem 43:27-40. doi:10.1021/jm9900321 (Pubitemid 30055761)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.1
, pp. 27-40
-
-
Pitts, W.J.1
Wityak, J.2
Smallheer, J.M.3
Tobin, A.E.4
Jetter, J.W.5
Buynitsky, J.S.6
Harlow, P.P.7
Solomon, K.A.8
Corjay, M.H.9
Mousa, S.A.10
Wexler, R.R.11
Jadhav, P.K.12
-
10
-
-
0034642520
-
3
-
DOI 10.1021/jm990049j
-
Batt DG, Petraitis JJ, Houghton GC, Modi DP, Cain GA, Corjay MH, Mousa SA, Bouchard PJ, Forsythe MS, Harlow PP, Barbera FA, Spitz SM, Wexler RR, Jadhav PK (2000) Disubstituted indazoles as potent antagonists of the integrin αvβ3. J Med Chem 43:41-58. doi:10.1021/jm990049j (Pubitemid 30055762)
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, Issue.1
, pp. 41-58
-
-
Batt, D.G.1
Petraitis, J.J.2
Houghton, G.C.3
Modi, D.P.4
Cain, G.A.5
Corjay, M.H.6
Mousa, S.A.7
Bouchard, P.J.8
Forsythe, M.S.9
Harlow, P.P.10
Barbera, F.A.11
Spitz, S.M.12
Wexler, R.R.13
Jadhav, P.K.14
-
11
-
-
0028600543
-
A simple and practical synthesis of 2-aminoimidazoles
-
doi:10.1021/jo00103a021
-
Little TL, Webber SE (1994) A simple and practical synthesis of 2-aminoimidazoles. J Org Chem 59:7299-7305. doi:10.1021/jo00103a021
-
(1994)
J Org Chem
, vol.59
, pp. 7299-7305
-
-
Little, T.L.1
Webber, S.E.2
-
12
-
-
8744318421
-
4 2-aminoimidazole alkaloids: Ab initio calculations, tautomerism, and reactivity
-
DOI 10.1021/ol048529e
-
Abou JR, Ghoulami S, Martin MT, Dau ETH, Travert N, Al-Mourabit A (2004) Biogenetically inspired synthesis of marine C6N4 2-aminoimidazole alkaloids: ab initio calculations, tautomerism, and reactivity. Org Lett 6:3933-3936. doi:10.1021/ol048529e (Pubitemid 39523256)
-
(2004)
Organic Letters
, vol.6
, Issue.22
, pp. 3933-3936
-
-
Abou-Jneid, R.1
Ghoulami, S.2
Martin, M.-T.3
Dau, E.T.H.4
Travert, N.5
Al-Mourabit, A.6
-
13
-
-
0142192558
-
The reaction of 5-acetyl-2-aminooxazole with amines: An approach to 1H-5-acetyl-2-aminoimidazoles
-
doi:10.1016/S0040-4039 01 81336-8
-
Lamattina JL, Mularski CJ (1984) The reaction of 5-acetyl-2-aminooxazole with amines: an approach to 1H-5-acetyl-2-aminoimidazoles. Tetrahedron Lett 25:2957-2960. doi:10.1016/S0040-4039 (01) 81336-8
-
(1984)
Tetrahedron Lett
, vol.25
, pp. 2957-2960
-
-
Lamattina, J.L.1
Mularski, C.J.2
-
14
-
-
15444365617
-
Recent developments in guanylating agents
-
Commemorative Issue in Honor of Prof. Nikolai Zefirov
-
Katritzky AR, Rogovoy B (2005) Recent developments in guanylating agents. Arkivoc Part iv: 49-87 and references herein. doi:10. 1002/chin. 200530277 (Pubitemid 40397747)
-
(2005)
Arkivoc
, vol.2005
, Issue.4
, pp. 49-87
-
-
Katritzky, A.R.1
Rogovoy, B.V.2
-
15
-
-
33750057704
-
Efficient Pd(0)-mediated microwave-assisted arylation of 2-substituted imidazo[1,2-a]pyrimidines
-
DOI 10.1021/cc060031b
-
Ermolat'ev DS, Giménez VN, Babaev EV, Van der Eycken E (2006) Efficient Pd (0)-mediated microwave-assisted arylation of 2-substituted imidazo[1, 2-a]pyrimidines. J Comb Chem 8:659-663. doi:10.1021/cc060031b (Pubitemid 44578621)
-
(2006)
Journal of Combinatorial Chemistry
, vol.8
, Issue.5
, pp. 659-663
-
-
Ermolat'ev, D.S.1
Gimenez, V.N.2
Babaev, E.V.3
Van Der Eycken, E.4
-
16
-
-
67650925523
-
Microwave-assisted synthesis of substituted 2-amino-1H-imidazoles from imidazo[1, 2-a]pyrimidines
-
doi:10.1016/j.tetlet.2009.06.128
-
Ermolat'ev DS, Svidritsky EP, Babaev EV, Van der Eycken E (2009) Microwave-assisted synthesis of substituted 2-amino-1H-imidazoles from imidazo[1, 2-a]pyrimidines. Tetrahedron Lett 50:5218-5220. doi:10.1016/j.tetlet. 2009.06.128
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 5218-5220
-
-
Ermolat'ev, D.S.1
Svidritsky, E.P.2
Babaev, E.V.3
Van Der Eycken, E.4
-
17
-
-
51549091184
-
A divergent synthesis of substituted 2-aminoimidazoles from 2-aminopyrimidines
-
doi:10.1021/jo8008758
-
Ermolat'ev DS, Van der Eycken E (2008) A divergent synthesis of substituted 2-aminoimidazoles from 2-aminopyrimidines. J Org Chem 73:6691-6697. doi:10.1021/jo8008758
-
(2008)
J Org Chem
, vol.73
, pp. 6691-6697
-
-
Ermolat'ev, D.S.1
Van Der Eycken, E.2
-
18
-
-
33846327230
-
Efficient one-pot two-step, microwave-assisted procedure for the synthesis of polysubstituted 2-aminoimidazoles
-
doi:10.1021/ol062421c
-
Ermolat'ev DS, Babaev EV, Van der Eycken E (2006) Efficient one-pot two-step, microwave-assisted procedure for the synthesis of polysubstituted 2-aminoimidazoles. Org Lett 8:5781-5784. doi:10.1021/ol062421c
-
(2006)
Org Lett
, vol.8
, pp. 5781-5784
-
-
Ermolat'ev, D.S.1
Babaev, E.V.2
Van Der Eycken, E.3
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