Biomimetic approach toward the stereoselective synthesis of acetogenins

Verfasser / Beitragende:
[R. V. A. Orru, Bas Groenendaal, J. van Heyst, Mark Hunting, C. Wesseling, R. F. Schmitz, S. F. Mayer, K. Faber]
Ort, Verlag, Jahr:
2003
Enthalten in:
Pure and Applied Chemistry, 75/2-3(2003-01-01), 259-264
Format:
Artikel (online)
ID: 378866206
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024 7 0 |a 10.1351/pac200375020259  |2 doi 
035 |a (NATIONALLICENCE)gruyter-10.1351/pac200375020259 
245 0 0 |a Biomimetic approach toward the stereoselective synthesis of acetogenins  |h [Elektronische Daten]  |c [R. V. A. Orru, Bas Groenendaal, J. van Heyst, Mark Hunting, C. Wesseling, R. F. Schmitz, S. F. Mayer, K. Faber] 
520 3 |a Acetogenins isolated from the Annonaceae family of tropical trees have drawn considerable attention owing to their broad spectrum of biological activities. They are structurally characterized by the presence of one to three tetrahydrofuran rings in the center of a long (partly hydroxylated) hydrocarbon chain that ends in a (functionalized) butenolide moiety. Here we describe some of our results toward the first asymmetric total synthesis of cis-gigantrionenin, a principal acetogenin. In this approach, an enzyme-catalyzed epoxide hydrolysis and an enzyme-triggered double cyclization are crucial and give stereoselective access to essential chiral building blocks. 
540 |a © 2013 Walter de Gruyter GmbH, Berlin/Boston 
700 1 |a Orru  |D R. V. A.  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
700 1 |a Groenendaal  |D Bas  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
700 1 |a van Heyst  |D J.  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
700 1 |a Hunting  |D Mark  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
700 1 |a Wesseling  |D C.  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
700 1 |a Schmitz  |D R. F.  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
700 1 |a Mayer  |D S. F.  |u Department of Chemistry, University of Graz, Heinrichstrasse 28, A-8010, Graz, Austria  |4 aut 
700 1 |a Faber  |D K.  |u Department of Chemistry, University of Graz, Heinrichstrasse 28, A-8010, Graz, Austria  |4 aut 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Groenendaal  |D Bas  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a van Heyst  |D J.  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hunting  |D Mark  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Wesseling  |D C.  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Schmitz  |D R. F.  |u Department of Chemistry, Vrije University Amsterdam, De Boelelaan 1083, NL-1081 HV, Amsterdam, The Netherlands  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Mayer  |D S. F.  |u Department of Chemistry, University of Graz, Heinrichstrasse 28, A-8010, Graz, Austria  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Faber  |D K.  |u Department of Chemistry, University of Graz, Heinrichstrasse 28, A-8010, Graz, Austria  |4 aut 
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