One-pot enantioselective synthesis of (S)-spirobrassinin and non-natural (S)-methylspirobrassinin from amino acids using a turnip enzyme
Author:
Funder
JSPS KAKENHI grant
Publisher
Springer Science and Business Media LLC
Subject
Molecular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11418-020-01468-9.pdf
Reference21 articles.
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2. Monde K, Osawa S, Harada N, Takasugi M, Suchy M, Kutschy P, Dzurilla M, Balentova E (2000) Synthesis and absolute stereochemistry of cruciferous phytoalexine, (–)-spirobrassinin. Chem Lett:886–887
3. Suchy M, Kutschy P, Monde K, Goto H, Harada N, Takasugi M, Dzurilla M, Balentová E (2001) Synthesis, absolute configuration, and enantiomeric enrichment of a cruciferous oxindole phytoalexin, (S)-(–)-spirobrassinin, and its oxazoline analog. J Org Chem 66:3940–3947
4. Ye N, Chen H, Wold EA, Shi PY, Zhou J (2016) Therapeutic potential of spirooxindoles as antiviral agents. ACS Infect Dis 2:382–392
5. Pilátová M, Šarišský M, Kutschy P, Miroššay A, Mezencev R, Čurillová Z, Suchý M, Monde K, Mirossay L, Mojžiš J (2005) Cruciferous phytoalexins: antiproliferative effects in T-Jurkat leukemic cells. Leuk Res 29:415–421
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