Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jessica Goller"'
Publikováno v:
European Journal of Organic Chemistry. 2019:895-899
Die enantioselektive Totalsynthese von Bischinolizidin-Alkaloiden: Ein modularer 'Inside-Out'-Zugang
Publikováno v:
Angewandte Chemie. 130:2456-2460
Publikováno v:
Angewandte Chemie (International ed. in English). 57(9)
Bisquinolizidine alkaloids are characterized by a chiral bispidine core (3,7-diazabicyclo[3.3.1]nonane) to which combinations of an α,N-fused 2-pyridone, an endo- or exo-α,N-annulated piperidin(on)e, and an exo-allyl substituent are attached. We de
Publikováno v:
European Journal of Organic Chemistry. 2019:862-862
Autor:
Dagmar Scharnagel, Jessica Goller, Matthias Breuning, Martin Eck, Felix Prause, Andreas Mueller, Wolfgang Milius
Publikováno v:
ChemInform. 47
A novel tricyclic bispidine ligand is prepared and successfully applied as a chiral ligand in Cu-catalyzed asymmetric Henry reactions.
Publikováno v:
Angewandte Chemie International Edition. 57:2261-2261
Publikováno v:
Angewandte Chemie. 130:2283-2283
Autor:
Wolfgang Milius, Matthias Breuning, Felix Prause, Martin Eck, Andreas Müller, Dagmar Scharnagel, Jessica Goller
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 21(35)
The first modular and flexible synthesis of core-chiral bispidines was achieved by using an "inside-out" strategy. The key intermediate, a NBoc-activated bispidine lactam, was constructed in enantiomerically pure form from a chirally modified β-amin