Journalartikel

Enantiomerically enriched trans-diols from alkenes in one pot: a multicatalyst approach


AutorenlisteHrdina, R; Müller, CE; Wende, RC; Wanka, L; Schreiner, PR

Jahr der Veröffentlichung2012

Seiten2498-2500

ZeitschriftChemical Communications

Bandnummer48

Heftnummer19

DOI Linkhttps://doi.org/10.1039/C2CC17435A

VerlagRoyal Society of Chemistry


Abstract

Multicatalysts consisting of non-natural oligopeptides with distinctly different catalytic moieties create molecular complexity in a multistep one-pot sequence starting from simple alkenes yielding highly enantiomerically enriched trans-diols.




Zitierstile

Harvard-ZitierstilHrdina, R., Müller, C., Wende, R., Wanka, L. and Schreiner, P. (2012) Enantiomerically enriched trans-diols from alkenes in one pot: a multicatalyst approach, Chemical Communications, 48(19), pp. 2498-2500. https://doi.org/10.1039/C2CC17435A

APA-ZitierstilHrdina, R., Müller, C., Wende, R., Wanka, L., & Schreiner, P. (2012). Enantiomerically enriched trans-diols from alkenes in one pot: a multicatalyst approach. Chemical Communications. 48(19), 2498-2500. https://doi.org/10.1039/C2CC17435A



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