Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sebastian Bretzke"'
Autor:
Sebastian Bretzke, Stephan Scheeff, Felicitas Vollmeyer, Friederike Eberhagen, Frank Rominger, Dirk Menche
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1111-1121 (2016)
The design, development and application of an efficient procedure for the concise synthesis of the 1,3-syn- and anti-tetrahydropyrimidine cores of manzacidins are reported. The intramolecular allylic substitution reaction of a readily available joint
Externí odkaz:
https://doaj.org/article/b8364cffa4dd4e7faa24c3dc56cf341b
Autor:
Friederike Eberhagen, Frank Rominger, Stephan Scheeff, Felicitas Vollmeyer, Sebastian Bretzke, Dirk Menche
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1111-1121 (2016)
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1111-1121 (2016)
The design, development and application of an efficient procedure for the concise synthesis of the 1,3-syn- and anti-tetrahydropyrimidine cores of manzacidins are reported. The intramolecular allylic substitution reaction of a readily available joint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fe621aa0492f76304021d152ba4e391
http://europepmc.org/articles/PMC4902044
http://europepmc.org/articles/PMC4902044
Autor:
Felicitas Vollmeyer, Frank Rominger, Sebastian Bretzke, Friederike Eberhagen, Stephan Scheeff, Dirk Menche
Publikováno v:
ChemInform. 47
The design, development and application of an efficient procedure for the concise synthesis of the 1,3-syn- and anti-tetrahydropyrimidine cores of manzacidins are reported. The intramolecular allylic substitution reaction of a readily available joint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f3b50e5973f32bd422bd7d8262418dd
https://doi.org/10.1002/chin.201640212
https://doi.org/10.1002/chin.201640212
Autor:
Olga Scherer, Sebastian Essig, Dirk Menche, Björn Schmalzbauer, Oliver Werz, Andreas Koeberle, Rolf Müller, Sebastian Bretzke
Publikováno v:
The Journal of organic chemistry. 81(4)
Full details on the evaluation and application of an easily feasible and generally useful method for configurational assignments of isolated methyl-bearing stereocenters are reported. The analytical tool relies on a bioinformatic gene cluster analysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e02ba3c7b145953a4aa163d9f8aef4f
https://pubmed.ncbi.nlm.nih.gov/26796481
https://pubmed.ncbi.nlm.nih.gov/26796481
Publikováno v:
Journal of the American Chemical Society. 134(47)
The stereochemical determination of the potent respiratory chain inhibitors ajudazols A and B and the total synthesis of ajudazol B are reported. Configurational assignment was exclusively based on biosynthetic gene cluster analysis of both ketoreduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ceb45132db96c17c9a77197b67dfa8d
https://pubmed.ncbi.nlm.nih.gov/23127125
https://pubmed.ncbi.nlm.nih.gov/23127125
Publikováno v:
ChemInform. 42
Depending on the choice of solvent either syn- or anti-diastereomers can be obtained as protected 1,3-diamine structures.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ae1754f75af4a825c533eb65cc440c3
https://doi.org/10.1002/chin.201107187
https://doi.org/10.1002/chin.201107187
Publikováno v:
Organic letters. 12(20)
An efficient protocol for the stereoselective synthesis of 1,3-syn and -anti-tetrahydropyrimidinones (syn- and anti-11a) is reported. The modular procedure is based on a stereodivergent cyclization of readily available urea-type substrates (10a) by i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf47d7d78447d8a94c918396a3aba2f2
https://pubmed.ncbi.nlm.nih.gov/20831256
https://pubmed.ncbi.nlm.nih.gov/20831256
Publikováno v:
Organic Letters; Oct2010, Vol. 12 Issue 20, p4494-4497, 4p