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@ARTICLE{Eichenauer:281034,
author = {Eichenauer, Nils C. and Nordschild, Anja C. M. and Bischop,
Martina and Schumacher, Dominik and Mackwitz, Marcel K. W.
and Tschersich, Roxanne and Wilhelm, Thorsten and
Pietruszka, Jörg},
title = {{T}otal {S}ynthesis of {S}olandelactones {A} and {B}},
journal = {European journal of organic chemistry},
volume = {2015},
number = {25},
issn = {1434-193X},
address = {Weinheim},
publisher = {Wiley-VCH Verl.},
reportid = {FZJ-2016-00745},
pages = {5620 - 5632},
year = {2015},
abstract = {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.},
cin = {IBOC / IBG-1-TA},
ddc = {540},
cid = {I:(DE-Juel1)IBOC-20090406 / I:(DE-Juel1)IBG-1-TA-20110204},
pnm = {89581 - Biotechnology (POF2-89581)},
pid = {G:(DE-HGF)POF2-89581},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000360064500016},
doi = {10.1002/ejoc.201500700},
url = {https://juser.fz-juelich.de/record/281034},
}