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Carreño, M. Carmen, Urbano, Antonio, Fischer, Jean (1997) Angucyclinone über enantioselektive Diels-Alder-Reaktionen zwischen (S)-2-(p-Tolylsulfinyl)-1,4-naphthochinon und substituierten, racemischen Vinylcyclohexenen. Angewandte Chemie, 109 (15). 1695-1697 doi:10.1002/ange.19971091514

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Reference TypeJournal (article/letter/editorial)
TitleAngucyclinone über enantioselektive Diels-Alder-Reaktionen zwischen (S)-2-(p-Tolylsulfinyl)-1,4-naphthochinon und substituierten, racemischen Vinylcyclohexenen
JournalAngewandte Chemie
AuthorsCarreño, M. CarmenAuthor
Urbano, AntonioAuthor
Fischer, JeanAuthor
Year1997 (August 4)Volume109
Issue15
PublisherWiley
DOIdoi:10.1002/ange.19971091514Search in ResearchGate
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Mindat Ref. ID7293595Long-form Identifiermindat:1:5:7293595:6
GUID0
Full ReferenceCarreño, M. Carmen, Urbano, Antonio, Fischer, Jean (1997) Angucyclinone über enantioselektive Diels-Alder-Reaktionen zwischen (S)-2-(p-Tolylsulfinyl)-1,4-naphthochinon und substituierten, racemischen Vinylcyclohexenen. Angewandte Chemie, 109 (15). 1695-1697 doi:10.1002/ange.19971091514
Plain TextCarreño, M. Carmen, Urbano, Antonio, Fischer, Jean (1997) Angucyclinone über enantioselektive Diels-Alder-Reaktionen zwischen (S)-2-(p-Tolylsulfinyl)-1,4-naphthochinon und substituierten, racemischen Vinylcyclohexenen. Angewandte Chemie, 109 (15). 1695-1697 doi:10.1002/ange.19971091514
In(1997, August) Angewandte Chemie Vol. 109 (15) Wiley

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Carreño, M. Carmen, Urbano, Antonio, Di Vitta, Claudio (2000) Enantioselective Diels-Alder Approach to C-3-Oxygenated Angucyclinones from (SS)-2-(p-Tolylsulfinyl)-1,4-naphthoquinone. Chemistry - A European Journal, 6 (5). 906-913 doi:10.1002/(sici)1521-3765(20000303)6:5<906::aid-chem906>3.0.co;2-g
Carreño, M. Carmen, García-Cerrada, Susana, Urbano, Antonio (2001) Enantiopure Dihydro-[5]-helicenequinones via Diels−Alder Reactions of Vinyl Dihydrophenanthrenes and (SS)-2-(p-Tolylsulfinyl)-1,4-benzoquinone. Journal Of The American Chemical Society, 123 (32) 7929-7930 doi:10.1021/ja010831k
Carreño, M. Carmen, Ribagorda, María, Somoza, Álvaro, Urbano, Antonio (2002) Enantioselective Total Synthesis of Angucyclinone-Type Antibiotics Rubiginones A2 and C2. Angewandte Chemie, 114 (15). 2879-2881 doi:10.1002/1521-3757(20020802)114:15<2879::aid-ange2879>3.0.co;2-h
Jana, Chandan Kumar, Studer, Armido (2007) Divergente Reaktionen an Racematen: katalytische, enantioselektive und regiodivergente Nitroso-Diels-Alder-Reaktionen. Angewandte Chemie, 119 (34). 6662-6664 doi:10.1002/ange.200701631
Carreño, M. Carmen, Ribagorda, María, Somoza, Álvaro, Urbano, Antonio (2002) Enantioselective Total Synthesis of Angucyclinone-Type Antibiotics Rubiginones A2 and C2. Angewandte Chemie International Edition, 41 (15). 2755-2757 doi:10.1002/1521-3773(20020802)41:15<2755::aid-anie2755>3.0.co;2-a
Evans, David A., Ripin, David H. Brown, Johnson, Jeffrey S., Shaughnessy, Eileen A. (1997) Neue Anwendung vonN-Acylimiden als chirale Auxiliare für Aldol- und Diels-Alder-Reaktionen - enantioselektive Synthese von α-Himachalen. Angewandte Chemie, 109 (19). 2208-2210 doi:10.1002/ange.19971091925
Bienaymé, Hugues (1997) Enantioselektive Diels-Alder-Cycloadditionen via Präorganisation an einem chiralen Lewis-Säure-Templat. Angewandte Chemie, 109 (23). 2785-2788 doi:10.1002/ange.19971092338
Carreño, M. Carmen, García-Cerrada, Susana, Urbano, Antonio (2003) From Central to Helical Chirality: Synthesis ofP andM Enantiomers of[5]Helicenequinones and Bisquinones from (SS)-2-(p-Tolylsulfinyl)- 1,4-benzoquinone. Chemistry - A European Journal, 9 (17). 4118-4131 doi:10.1002/chem.200304835
Charette, André B., Lemay, Jacinthe (1997) Diastereo- und enantioselektive Synthese von 1,2,3-substituierten Cyclopropanen mit Zinkcarbenoiden. Angewandte Chemie, 109 (10). 1163-1165 doi:10.1002/ange.19971091029
Stocking, Emily M., Williams, Robert M. (2003) Chemie und Biologie natürlicher Diels-Alder-Reaktionen. Angewandte Chemie, 115 (27). 3186-3223 doi:10.1002/ange.200200534
Tobey, S. W., Law, D. C. F. (1968) Diels-Alder-Reaktionen von Tetrahalogencyclopropenen. Angewandte Chemie, 80 (15). 636 doi:10.1002/ange.19680801542
 
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