Bioinspired catalytic generation of main-group electrophiles by cooperative bond activation

9Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Catalytic processes involving cooperativity have seen tremendous progress in recent years and impressive new synthetic methodologies have been developed. Inspired by the cooperative heterolytic H2 splitting in [NiFe] hydrogenases, Ohki and Tatsumi designed cationic ruthenium thiolate complexes with a tethered sulfur ligand. Over the last decade, we have demonstrated the facile activation of main-group hydrides such as hydrosilanes, hydroboranes, DIBAL–H, and hydrostannanes by the Ru–S bond in Ohki–Tatsumi complexes. This account illustrates these E–H bond activations and highlights selected catalytic applications, particularly dehydrocouplings, of the generated main-group electrophiles.

Cite

CITATION STYLE

APA

Forster, F., & Oestreich, M. (2018). Bioinspired catalytic generation of main-group electrophiles by cooperative bond activation. Chimia, 72(9), 584–588. https://doi.org/10.2533/chimia.2018.584

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free