Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Björn Schmalzbauer"'
Publikováno v:
Organic letters. 21(6)
The enantioselective total synthesis of (+)-salimabromide was accomplished by a concise two-step conversion of the fully functionalized dibromo-tetraline core, involving a one-pot Baeyer-Villiger/allylic oxidation by an innovative radical reagent com
Autor:
Dirk Menche, Björn Schmalzbauer
Publikováno v:
Organic Letters. 17:2956-2959
A concise synthesis of the tricyclic core 2 of the structurally unique marine myxobacterial natural product salimabromide has been developed. Compound 2 contains the tetraline subunit including the two quaternary centers and the eight-membered ring o
Publikováno v:
Organic Letters. 15:964-967
A concise total synthesis of dysidavarone A possessing the new "dysidavarane" carbon skeleton has been accomplished by a convergent strategy, involving a stereoselective reductive alkylation of a Wieland-Miescher type ketone under Birch conditions an
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