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000281034 1001_ $$0P:(DE-HGF)0$$aEichenauer, Nils C.$$b0
000281034 245__ $$aTotal Synthesis of Solandelactones A and B
000281034 260__ $$aWeinheim$$bWiley-VCH Verl.$$c2015
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000281034 520__ $$aThe 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.
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000281034 7001_ $$0P:(DE-HGF)0$$aNordschild, Anja C. M.$$b1
000281034 7001_ $$0P:(DE-HGF)0$$aBischop, Martina$$b2
000281034 7001_ $$0P:(DE-HGF)0$$aSchumacher, Dominik$$b3
000281034 7001_ $$0P:(DE-HGF)0$$aMackwitz, Marcel K. W.$$b4
000281034 7001_ $$0P:(DE-HGF)0$$aTschersich, Roxanne$$b5
000281034 7001_ $$0P:(DE-HGF)0$$aWilhelm, Thorsten$$b6
000281034 7001_ $$0P:(DE-Juel1)128906$$aPietruszka, Jörg$$b7$$eCorresponding author$$ufzj
000281034 773__ $$0PERI:(DE-600)1475010-7$$a10.1002/ejoc.201500700$$gVol. 2015, no. 25, p. 5620 - 5632$$n25$$p5620 - 5632$$tEuropean journal of organic chemistry$$v2015$$x1434-193X$$y2015
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