Zobrazeno 1 - 10
of 22
pro vyhledávání: '"1-phenylpropene"'
Publikováno v:
Chemical and Pharmaceutical Bulletin. 43:1267-1271
The BF3-, TsOH- or HCOOH-catalyzed dimerization of 3, 4-dioxygenated cinnamate or 1-arylpropene offers a route to arylindane lignans. The structures of the products were elucidated and a mechanism is proposed for the reactions. The structures of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::baa018dfdae3c22ccf8455062902dbc3
https://doi.org/10.1248/cpb.43.1267
https://doi.org/10.1248/cpb.43.1267
Autor:
James A. Walker, Wing. Tsang
Publikováno v:
Symposium (International) on Combustion. 25:867-874
The reactions of hydrogen atom with 1-phenylpropene (IPP) have been studied in single-pulse shocktubeexperiments. Contribution from a large number of the possible reactive channels has been observed. The prime channels are the displacement of the met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84c47d5ed2adfaa81b9317e706e48c0a
https://doi.org/10.1016/s0082-0784(06)80721-6
https://doi.org/10.1016/s0082-0784(06)80721-6
Publikováno v:
ChemInform. 21
The title enamine may exist in two double bond isomers. Both forms react with the nitroolefins under different conditions to afford, after hydrolysis, regioisomeric ℘-nitroketones. ℘-Dicarbonyl compounds are isolated from the hydrolysis at pH 2 o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cc63087da9c3e89caafc216b2428258
https://doi.org/10.1002/chin.199001062
https://doi.org/10.1002/chin.199001062
Autor:
Dario M. Bassani, Frederick D. Lewis
Publikováno v:
Journal of the American Chemical Society. 115:7523-7524
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fabacd978f975a4662e5d488d4bf4c74
https://doi.org/10.1021/ja00069a070
https://doi.org/10.1021/ja00069a070
Autor:
Dennis G. Garratt, George H. Schmid
Publikováno v:
Canadian Journal of Chemistry. 52:3599-3606
2,4-Dinitrophenylselenium trichloride has been found to add to cis- and trans-1-phenylpropene in an anti stereospecific manner to yield threo-dl-and erythro-dl-β-chloroalkyl 2,4-dinitrophenyl selenide dichlorides, respectively. Comparison is made wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a253b5b3582dcf3998fd513a1fcc819
https://doi.org/10.1139/v74-538
https://doi.org/10.1139/v74-538
Autor:
Dennis G. Garratt
Publikováno v:
Canadian Journal of Chemistry. 57:2180-2184
The reaction of benzeneselenenyl thiocyanate with E- and Z-1-phenylpropene has been shown to give products under conditions of kinetic control of net stereospecific syn addition in the Markownikoff orientation. Furthermore, the reactions were highly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b2b18cf5585fa4c86be1599de6dbf74
https://doi.org/10.1139/v79-349
https://doi.org/10.1139/v79-349
Publikováno v:
The Journal of Organic Chemistry. 43:1656-1660
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4af096627db6fb21bab60e564ffe63ca
https://doi.org/10.1021/jo00403a007
https://doi.org/10.1021/jo00403a007
Publikováno v:
Tetrahedron. 43:3279-3287
The reactions between the nitroolefin with enamines from cycloalkanones have been studied. No ring-chain tautomerism between the title heterocycles and the nitroalkylated enamines has been found, in contrast with the case of the isomeric 2-nitro 1-ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::025240c55121af4989d1276a76134dc8
https://doi.org/10.1016/s0040-4020(01)90296-0
https://doi.org/10.1016/s0040-4020(01)90296-0
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1518-1523
Reactions of cyclic and acyclic nitrones and nitrile oxides with 1,2-dihydronaphthalene, indene, and trans-1-phenylpropene give rise to mixtures of regioisomers. The results are analysed on the basis of frontier orbital interactions and the steric re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d477eed57f392a3d850318d8482346a3
https://doi.org/10.1039/p19760001518
https://doi.org/10.1039/p19760001518
Publikováno v:
Canadian Journal of Chemistry. 50:2457-2464
The thero-anti-Markownikoff and threo-Markownikoff adducts are the products of addition of 4-chloro-and 2,4-dinitrobenzenesulfenyl chloride to cis-1-phenylpropene while only the erythro Markownikoff adduct is the product of addition to trans-1-phenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::939efe25162d66df0c57362e02ff2e8a
https://doi.org/10.1139/v72-396
https://doi.org/10.1139/v72-396