dc.creator | Augusti R. | |
dc.creator | Kascheres C. | |
dc.date | 1994 | |
dc.date | 2015-06-26T17:27:53Z | |
dc.date | 2015-11-26T14:22:44Z | |
dc.date | 2015-06-26T17:27:53Z | |
dc.date | 2015-11-26T14:22:44Z | |
dc.date.accessioned | 2018-03-28T21:24:39Z | |
dc.date.available | 2018-03-28T21:24:39Z | |
dc.identifier | | |
dc.identifier | Tetrahedron. , v. 50, n. 23, p. 6723 - 6726, 1994. | |
dc.identifier | 404020 | |
dc.identifier | 10.1016/S0040-4020(01)81328-4 | |
dc.identifier | http://www.scopus.com/inward/record.url?eid=2-s2.0-0028128611&partnerID=40&md5=0876af38524126ec17fe285c12496d96 | |
dc.identifier | http://www.repositorio.unicamp.br/handle/REPOSIP/96419 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/96419 | |
dc.identifier | 2-s2.0-0028128611 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1244914 | |
dc.description | The synthetic usefulness of a new method of 1,2,3-triazole synthesis has been demonstrated. By employing cyclic enamino esters 3 and enamino ketones 4 in reactions with 5,7-dinitro-3-diazo-1,3-dihydro-2H-indol-2-one (1), bicyclic triazoles 5 and 6 have been prepared in good to excellent yields. © 1994. | |
dc.description | 50 | |
dc.description | 23 | |
dc.description | 6723 | |
dc.description | 6726 | |
dc.description | Augusti, Kascheres, (1993) J. Org. Chem., 58, p. 7079 | |
dc.description | Greenhill, Enaminones (1990) Chemical Society Reviews, 6, p. 277 | |
dc.description | Sainsbury, (1984) Rodd's Chemistry of Carbon Compounds, 4 (500). , M.F. Ansell, Elsevier, New York (NY), Chapter 18 | |
dc.description | Wamhoff, (1984) Comprehensive Heterocyclic Chemistry, 5, p. 669. , K.T. Potts, Pergamon Press, Oxford | |
dc.description | Grundmann, Haldenwanger, Über die Gefahren beim Umgang mit Methylazid (1950) Angewandte Chemie, 62, p. 410 | |
dc.description | Katritzky, Lagowski, (1984) Comprehensive Heterocyclic Chemistry, 5, p. 39. , For example, 1,2,3-triazoles are much less reactive than pyrroles in electrophilic aromatic substitution, see:, K.T. Potts, Pergamon Press, Oxford | |
dc.description | Anderson, McPherson, New, Rick, (1984) J. Med. Chem., 27, p. 1321 | |
dc.description | Anderson, Bhattacharjee, Houston, (1989) J. Med. Chem., 32, p. 119 | |
dc.description | Anderson, Corey, (1977) J. Med. Chem., 20, p. 812 | |
dc.description | Mattocks, Pyrrolizidine alkaloid analogues. Part 2. Further hydroxymethyl-1-methyl-3-pyrrolines (synthanecines), and the preparation and esterification of some hydroxymethylpyrroles (1978) Journal of the Chemical Society, Perkin Transactions 1, p. 896 | |
dc.description | Ladurée, Lancelot, Robba, Chenu, Mathé, Synthesis and evaluation of antileukemic activity of 5-thienyl- or 5-(2-furyl)-2,3-dihydro-6,7-bis(hydroxymethyl)-1H-pyrrolizine bis(alkylcarbamates) and derivatives (1989) Journal of Medicinal Chemistry, 32, p. 456 | |
dc.description | Anderson, Chang, McPherson, (1983) J. Med. Chem., 26, p. 1333 | |
dc.description | Barbour, Robins, Pyrrolizidine alkaloid analogues. Synthesis of 11-membered macrocyclic diesters of (�)-synthanecine A (1985) Journal of the Chemical Society, Perkin Transactions 1, p. 2475 | |
dc.description | Zalkow, Glinski, Gelbaum, Moore, Melder, Powis, Semisynthetic pyrrolizidine alkaloid N-oxide antitumor agents. Esters of heliotridine (1985) Journal of Medicinal Chemistry, 31, p. 1520 | |
dc.description | Anderson, Halat, (1979) J. Med. Chem., 22, p. 977 | |
dc.description | Anderson, McPherson, (1982) J. Med. Chem., 25, p. 84 | |
dc.description | Zalkow, Glinski, Gelbaum, Fleischmann, McGrowan, Gordon, (1985) J. Med. Chem., 28, p. 687 | |
dc.description | Anderson, Corey, (1977) J. Med. Chem., 20, p. 1691 | |
dc.description | Anderson, Halat, Rick, (1980) J. Med. Chem., 23, p. 87 | |
dc.description | Lalezari, Schwartz, (1988) J. Med. Chem., 31, p. 1427 | |
dc.description | Pearson, Bergmeier, Chytra, The Synthesis of Triazole Analogues of Antitumor Dehydropyrrolizidine Alkaloids (1990) Synthesis, p. 156 | |
dc.description | Jones, Sliskovic, (1983) Advances in Heterocyclic Chemistry, 34, p. 79. , A.R. Katritzky, Academic Press, New York (NY) | |
dc.description | Seebach, Enders, Rolf, Reimund, Reaktion metallierter Nitrosamine mit Nitrilen Eine neue Methode zur Darstellung von υ-Triazolen (1977) Chemische Berichte, 110, p. 1879 | |
dc.description | Regitz, Schwall, Reaktionen CH-aktiver Verbindungen mit Aziden, XXVI Synthese von α-Diazo-iminen und isomeren 1.2.3-Triazolen sowie deren Umwandlung in α-Diazo-immoniumsalze2 (1969) Justus Liebigs Annalen der Chemie, 728, p. 99 | |
dc.description | Baum, Shork, Davies, Smith, Diazotransfer Reactions withp-Acetamidobenzenesulfonyl Azide (1987) Synthetic Communications, 17 (14), p. 1709 | |
dc.description | Celérier, Deloisy, Lhommet, Maitte, Lactim ether chemistry. Cyclic .beta.-enamino ester synthesis (1979) The Journal of Organic Chemistry, 44, p. 3089 | |
dc.description | Chen, Mariano, Little, O'Brien, Huesmann, Electron-transfer-initiated photospirocyclization reactions of .beta.-enaminone-derived allyliminium salts (1984) The Journal of Organic Chemistry, 49 (2), p. 220 | |
dc.description | Coretts, Hindmarsh, Mah, Preparation and properties of 5-nitro-, 7-nitro-, and 5,7-dinitrooxindole (1970) Canadian Journal of Chemistry, 48, p. 3747 | |
dc.language | en | |
dc.publisher | | |
dc.relation | Tetrahedron | |
dc.rights | fechado | |
dc.source | Scopus | |
dc.title | Bicyclic Triazoles From A Diazo Transfer Reaction Between Cyclic Enaminones And 5,7-dinitro-3-diazo-1,3-dihydro-2h-indol-2-one | |
dc.type | Artículos de revistas | |