Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Zev Lidert"'
Publikováno v:
Journal of Heterocyclic Chemistry. 38:645-648
The reaction of an N-monosubstituted amidine with a β-ketoester to afford a pyrimidinone is sluggish at best under normal conditions. We now report that this reaction can be effected in moderate yield under high pressure. Thus, 2,6-dichloro-4-pyridy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6caa98352650559ad02b5676084b2212
https://doi.org/10.1002/jhet.5570380316
https://doi.org/10.1002/jhet.5570380316
Autor:
Richard K Jansson, Glenn Richard Carlson, Tarlochan S. Dhadialla, Ricky Hunter, Zev Lidert, Richard A. Slawecki, Christine S. Jany
Publikováno v:
Pest Management Science. 57:115-119
Methoxyfenozide [N-tert-butyl-N'-(3-methoxy-o-toluoyl)-3,5-xylohydrazide; RH-2485] is the newest diacylhydrazine insecticide to reach the marketplace. It binds with very high affinity to the ecdysone receptor complex (EcR:USP) in lepidopteran insects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bce569d6e4ebae8b7c7e9df65509bdf8
https://doi.org/10.1002/1526-4998(200102)57:2<115::aid-ps245>3.0.co
https://doi.org/10.1002/1526-4998(200102)57:2<115::aid-ps245>3.0.co
Autor:
Mary G. Johnson, David Hamilton Young, Zev Lidert, Barry Clifford Lange, Raj J. Mehta, Colin Swithenbank, Samuel Eugene Sherba, Margaret M. Bowers-Daines, Susan L. Morris-Natschke, Hiroshi Kiyokawa, Kuo Hsiung Lee
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:3153-3158
1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione (1) and related derivatives were assayed for antifungal, antimicrobial, and plant growth regulatory activity. Compound 1 was extremely potent against several strains of fungi, bacteria, and algae (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c09d28f425a5c5d9b49317c2765e674
https://doi.org/10.1016/s0960-894x(97)10176-7
https://doi.org/10.1016/s0960-894x(97)10176-7
Publikováno v:
Tetrahedron Letters. 38:4339-4342
A novel synthesis of the promising new herbicide 2-(2,6-dichloro-4-pyridyl)-3-propargyl-5-ethyl-6-methyl-4(3 H )-pyrimidinone (12) is reported which features (1) regioselective carbon, followed by nitrogen, dialkylation of an intermediate dianion, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f39f458e861b63c7b62ca424e05c6c1
https://doi.org/10.1016/s0040-4039(97)00946-5
https://doi.org/10.1016/s0040-4039(97)00946-5
Autor:
Zev Lidert, Adrian L. Smith, Andrew B. Holmes, Leslie R. Hughes, Simon F. Williams, Colin Swithenbank
Publikováno v:
ChemInform. 22
The racemates of indolizidine 167B (X), 205A (XVI) and 207A (XVII) as well as (-)-indolizidine 209B (XXVI) are prepared as shown using a general strategy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e6aa2372e930d24ec54c93ce4132b4c
https://doi.org/10.1002/chin.199128227
https://doi.org/10.1002/chin.199128227
Publikováno v:
ChemInform. 28
A novel synthesis of the promising new herbicide 2-(2,6-dichloro-4-pyridyl)-3-propargyl-5-ethyl-6-methyl-4(3 H )-pyrimidinone (12) is reported which features (1) regioselective carbon, followed by nitrogen, dialkylation of an intermediate dianion, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef875e8c4cd6ba5cc57ece909457331b
https://doi.org/10.1002/chin.199738194
https://doi.org/10.1002/chin.199738194
Publikováno v:
ChemInform. 32
The reaction of an N-monosubstituted amidine with a β-ketoester to afford a pyrimidinone is sluggish at best under normal conditions. We now report that this reaction can be effected in moderate yield under high pressure. Thus, 2,6-dichloro-4-pyridy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12a6af05f31fa959def198cb7592cbd3
https://doi.org/10.1002/chin.200141177
https://doi.org/10.1002/chin.200141177
Autor:
Vallapa Chittawong, C. Swithenbank, Zev Lidert, D. H. Miles, J. M. R. Del Medeiros, P. A. Hedin, James A. Weeks, Jerry L. Atwood
Publikováno v:
Journal of Natural Products. 53:1548-1551
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1d2513d5acc35a82c7ef8f6cab2b6c1
https://doi.org/10.1021/np50072a023
https://doi.org/10.1021/np50072a023
Autor:
David Randazzo, Colin Swithenbank, Zev Lidert, Bradford C. Vanwagenen, Raymond D. Larsen, John H. Cardellina
Publikováno v:
The Journal of Organic Chemistry. 58:335-337
Ulosantoin (2), a phosphorylated hydantoin, has been isolated from organic soluble extracts of the sponge Ulosa ruetzleri and found to exhibit marked insecticidal activity against tobacco hornworm larvae and cockroaches. The structure was determined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81cdece0bffceb1d993b421575c09e05
https://doi.org/10.1021/jo00054a013
https://doi.org/10.1021/jo00054a013