%0 Journal Article
%A Eichenauer, Nils C.
%A Nordschild, Anja C. M.
%A Bischop, Martina
%A Schumacher, Dominik
%A Mackwitz, Marcel K. W.
%A Tschersich, Roxanne
%A Wilhelm, Thorsten
%A Pietruszka, Jörg
%T Total Synthesis of Solandelactones A and B
%J European journal of organic chemistry
%V 2015
%N 25
%@ 1434-193X
%C Weinheim
%I Wiley-VCH Verl.
%M FZJ-2016-00745
%P 5620 - 5632
%D 2015
%X The total synthesis of solandelactones A and B is presented. The eastern cyclopropyl moiety was prepared following an exceptionally short chemoenzymatic approach whereas enantioselective synthesis of the western side-chain relied on the application of diastereomerically pure allyl boronates. The natural products solandelactones A and B were isolated in good overall yields following convergence of each eastern and western element by application of the Nozaki–Hiyama–Kishi reaction.
%F PUB:(DE-HGF)16
%9 Journal Article
%U <Go to ISI:>//WOS:000360064500016
%R 10.1002/ejoc.201500700
%U https://juser.fz-juelich.de/record/281034