Journal Article

FZJ-2016-00745

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Total Synthesis of Solandelactones A and B

Eichenauer, N. C. ; Nordschild, A. C. M. ; Bischop, M. ; Schumacher, D. ; Mackwitz, M. K. W. ; Tschersich, R. ; Wilhelm, T. ; Pietruszka, J. (Corresponding author)FZJ*

2015
Wiley-VCH Verl. Weinheim

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Please use a persistent id in citations: doi:10.1002/ejoc.201500700

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.

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Contributing Institute(s):

1. Institut für Bioorganische Chemie (HHUD) (IBOC)
2. Biotechnologie Technische und administrative Infrastruktur IBG-1 (IBG-1-TA)

Research Program(s):

1. 89581 - Biotechnology (POF2-89581) (POF2-89581)

Appears in the scientific report 2015

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Database coverage:
; Current Contents - Physical, Chemical and Earth Sciences ; IF < 5 ; JCR ; NCBI Molecular Biology Database ; No Authors Fulltext ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection

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