Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kurt Kiewel"'
Autor:
Fabrice Lefevre, Beat Wirz, Marvin M. Hansen, Manuela Avi, Van Martin, David Mangan, Antonio Osorio-Lozada, Steven P. Hanlon, Stephan Luetz, John W. Wong, Hans-Peter Meyer, Matthias Kittelmann, Radka Snajdrova, Hans Iding, Thomas Michael Eckrich, Cecilia Branneby, Joseph P. Adams, Kurt Laumen, Thomas S. Moody, Ian Fotheringham, Karen Robins, Karen E. Holt-Tiffin, Andrew J. Collis, Roger M. Howard, Rob ter Halle, Andrew S. Wells, Peter W. Sutton, Daniel Auriol, Gjalt W. Huisman, Ian Archer, Bruno Dumas, Ernst Kupfer, Kurt Kiewel, Matthew D. Truppo
Publikováno v:
Practical Methods for Biocatalysis and Biotransformations 2
Peter W. Sutton, Joseph P. Adams, Ian Archer, Daniel Auriol, Manuela Avi, Cecilia Branneby, Andrew J. Collis, Bruno Dumas, Thomas Eckrich, Ian Fotheringham, Rob ter Halle, Steven Hanlon, Marvin Hansen, K. E. Holt-Tiffin, Roger M. Howard, Gjalt W. Hui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77fafea9a76d66d13099ed7279022ae8
https://doi.org/10.1002/9781119943426.ch1
https://doi.org/10.1002/9781119943426.ch1
Publikováno v:
Organic Letters. 7:5163-5165
[reaction: see text] A stereocontrolled synthesis of the DE fragment (2) of the marine alkaloid upenamide (1) is described. The synthesis proceeds in 12 steps from caprolactone (10) and 20-25% overall yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e8ebbe9d360e341acfd0a6fa93d6fe
https://doi.org/10.1021/ol051993e
https://doi.org/10.1021/ol051993e
Publikováno v:
Tetrahedron Letters. 42:6621-6623
Asymmetric intramolecular Heck cyclization of endocyclic enamides occurs at room temperature to give indoloizidine and azaazulene ring systems in up to 86% enantiomeric excess. A synthesis of (+)-epiindolizidine 167B and formal synthesis of 5 E ,9 Z
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85ce34561bb041b93d983045e3e5feea
https://doi.org/10.1016/s0040-4039(01)01361-2
https://doi.org/10.1016/s0040-4039(01)01361-2
Publikováno v:
ChemInform. 31
A PCP-type catalyst was prepared and examined within the context of intramolecular Heck reactions. A substrate possessing a 1,4-diene system effectively poisoned the PCP catalyst leading to no reaction. This behavior contrasts with the typical pallad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::802d28696669507eeed9ff1b459ae992
https://doi.org/10.1002/chin.200010025
https://doi.org/10.1002/chin.200010025
Publikováno v:
ChemInform. 32
Asymmetric intramolecular Heck cyclization of endocyclic enamides occurs at room temperature to give indoloizidine and azaazulene ring systems in up to 86% enantiomeric excess. A synthesis of (+)-epiindolizidine 167B and formal synthesis of 5 E ,9 Z
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e7d6a2fd48496a6d241461202473cb2
https://doi.org/10.1002/chin.200150200
https://doi.org/10.1002/chin.200150200
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::698b693cb9d4a77fcbd91425645a944a
https://doi.org/10.1002/chin.200613199
https://doi.org/10.1002/chin.200613199