Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Rainer, Rieger"'
Publikováno v:
Ideen- und Innovationsmanagement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::857f3e75d32c2911b3364968cb1d5936
https://doi.org/10.37307/j.2198-3151.2016.02.04
https://doi.org/10.37307/j.2198-3151.2016.02.04
Publikováno v:
Journal of Polymer Science Part A: Polymer Chemistry. 37:677-682
With the development of methods to support metallocenes and methylaluminoxane cocatalysts on suitable carriers, it became possible to combine the specific advantages of homogeneous metallocene catalysis with those of heterogeneous Ziegler catalysts i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6537183dd6767fe62c9026f3898a705b
https://doi.org/10.1002/(sici)1099-0518(19990301)37:5<677::aid-pola18>3.0.co
https://doi.org/10.1002/(sici)1099-0518(19990301)37:5<677::aid-pola18>3.0.co
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2904de48ce4603a585f15d548ce2b03b
https://doi.org/10.1002/chin.199212243
https://doi.org/10.1002/chin.199212243
Publikováno v:
Liebigs Annalen der Chemie. 1991:1343-1346
Enantioselective Terpene Syntheses by Diels-Alder Reaction of 1-(1-Arylalkoxy)-2-methyl-1,3-butadiene with Isoprene The (R)- and (S)-1-(1-arylalkoxy)-2-methyl-1,3-butadienes 6 undergo [4 + 2] cycloadditions with excess isoprene (7) under pressure to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e2333c364d9f9788158aa3ed0b40a5a
https://doi.org/10.1002/jlac.1991199101229
https://doi.org/10.1002/jlac.1991199101229
Autor:
Eberhard Breitmaier, Rainer Rieger
Publikováno v:
Synthesis. 1990:697-701
Chiral 1-arylethanols , prepared by enantioselective reduction of phenones with lithium aluminium hydride and (2S,3R)-(+)-4-dimethylamino-1,2-diphenyl-3-methylbutanol, are converted to the chiral 2-methyl-1-(1-arylethoxy)1,3-butadienes (I) by vinylog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0dc221a1bbe93394f468d2ba747a827f
https://doi.org/10.1055/s-1990-26986
https://doi.org/10.1055/s-1990-26986
By means of temperature-dependent multinuclear NMR studies, electrical conductivity measurements and polymerization activity assessments, the nature of the resulting complexes formed between metallocene alkyls or metallocene dihalides and Group 13 Le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af2b089eea7f7b41fdabb4c799bad233
https://doi.org/10.1016/s0167-2991(08)63037-2
https://doi.org/10.1016/s0167-2991(08)63037-2
