Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Michael Casutt"'
Autor:
Werner Bonrath, Kun Peng, Le Dai, Bo Gao, Angelika Friedel, Ines Warnke, Gilberto Litta, Michael Casutt, Thomas Koppe, Michael Schwarz, Thomas Netscher
Publikováno v:
Ullmann's Encyclopedia of Industrial Chemistry. :1-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01e51c6b03f5d6864dab51413ebcf0e9
https://doi.org/10.1002/14356007.o27_o12.pub2
https://doi.org/10.1002/14356007.o27_o12.pub2
Publikováno v:
Ullmann's Encyclopedia of Industrial Chemistry
The article contains sections titled: 1. Introduction 2. History 3. Physical and Chemical Properties 4. Occurrence 5. Biosynthesis 6. Function as Prosthetic Group 7. Isolation and Production 8. Metabolism and Importance for the Organism 9. Deficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db8c15c1e02803a09a2e0efb8a352b87
https://doi.org/10.1002/14356007.o27_o12
https://doi.org/10.1002/14356007.o27_o12
Publikováno v:
ChemInform. 25
A new synthesis of 1-alkylimidazole-5-carbaldehydes starting from [3-(dimethylamino)-2-azaprop-2-enylidene]dimethylammonium chloride and alkyl N-alkylglycinate is described
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::157a24406af35809bb4bfb29ff63c6d2
https://doi.org/10.1002/chin.199436155
https://doi.org/10.1002/chin.199436155
Publikováno v:
Liebigs Annalen der Chemie. 1990:233-238
Allo-, Epiallo-, and Pseudoyohimbanes as well as Heteroyohimbanes by Reaction of a Tetracyclic Aldehyde with Acetoacetate in Different Solvents The reaction of methyl acetoacetate with 4 in CH3OH/ CH3ONa leads to 11 and 12 with yohimbane skeleton but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb4f78a3db218de513138ef189e76555
https://doi.org/10.1002/jlac.199019900142
https://doi.org/10.1002/jlac.199019900142
Publikováno v:
Angewandte Chemie International Edition in English. 34:2391-2393
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76bd88b8f255d6e87d1c8162aecc1baf
https://doi.org/10.1002/anie.199523911
https://doi.org/10.1002/anie.199523911
Publikováno v:
Angewandte Chemie. 107:2582-2584
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29bb8c24ea3e8e47861dca16667843b0
https://doi.org/10.1002/ange.19951072116
https://doi.org/10.1002/ange.19951072116
Autor:
Manfred Eggersdorfer, Geo Adam, Michael John, Wolfgang Hähnlein, Ludvik Labler, Kai-U. Baldenius, Linda von dem Bussche-Hünnefeld, Eckhard Hilgemann, Peter Hoppe, Rainer Stürmer, Fritz Weber, August Rüttimann, Gérard Moine, Hans-Peter Hohmann, Roland Kurth, Joachim Paust, Horst Pauling, Bernd-Jürgen Weimann, Bruno Kaesler, Bernd Oster, Ulrich Fechtel, Klaus Kaiser, Bernd de Potzolli, Michael Casutt, Thomas Koppe, Michael Schwarz, Urs Hengartner, Antoine de Saizieu, Christof Wehrli, René Blum
Publikováno v:
Ullmann's Encyclopedia of Industrial Chemistry ISBN: 3527306730
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e37ee72ccac1e5b88ba73dd62e44c9dd
https://doi.org/10.1002/14356007.a27_443
https://doi.org/10.1002/14356007.a27_443
Publikováno v:
Synthesis. 1994:247-248
A new synthesis of 1-alkylimidazole-5-carbaldehydes starting from [3-(dimethylamino)-2-azaprop-2-enylidene]dimethylammonium chloride and alkyl N-alkylglycinate is described
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9495c6abe5b38d8deb632c2102b5d12
https://doi.org/10.1055/s-1994-25449
https://doi.org/10.1055/s-1994-25449
Autor:
Michael Casutt, Peter Rosenmund
Publikováno v:
Tetrahedron Letters. 24:1771-1774
The key step in this synthesis, basing on the toluene-tricarbonylchrome promoted 1.4-H2 addition on the diene 7, proceeds with nearly 100 per cent yield and full stereoselectivity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bba3ec6a15afd7bec4e9fe55a24b3d1e
https://doi.org/10.1016/s0040-4039(00)81766-9
https://doi.org/10.1016/s0040-4039(00)81766-9