Abstract:
Since the discovery of ylides more than 100 years ago, this class of compounds has developed to versatile reagents in organic synthesis.[1] While early days were particularly coined by the advent of Wittig and Wittig-type olefination reactions,[2] they are nowadays applied in many stoichiometric and catalytic transformations.[3] Also their α-metalated congener - the so-called yldiides - have early attracted research interest due to their strong nucleophilicity and potential use as versatile building blocks. However, selective applications long remained challenging because of their high reactivity, often observed unselective and difficult preparation on ain larger scale.
In the past years, our group has reported on the synthesis and reactivity of α-metalated ylides (1). Owing to their highly nucleophilic character these compounds turned out to be excellent precursors to access electron-rich phosphines with beneficial properties for homogeneous catalysis[4] and to stabilize electron-deficient main group species.[5] Most recently, we uncovered that metalated ylides can also react as coordination complexes of carbon to readily exchange the phosphine substituent withby carbon monoxide.[6] This remarkable reactivity provided access to reactive species such as ketenyl anions 2 which have long been regarded as fleeting intermediates, but proven sufficiently stable to serve as starting materials to a variety of carbonyl compounds. Here, we will summarize this unique reactivity of metalated ylides.
References
[1] A. Michaelis, H. V. Gimborn, Ber. 1894, 27, 272.
[2] G. Wittig, G. Geissler, Liebigs Ann. 1953, 580, 44.
[3] O. I. Kolodiazhnyi in Phosphorus Ylides: Chemistry and Application in Organic Synthesis, Wiley-VCH, Weinheim, 1999.
[4] a) T. Scherpf, R. Wirth, S. Molitor, K.-S. Feichtner, V. H. Gessner, Angew. Chem. Int. Ed. 2015, 54, 8542. b) S. Lapointe, A. Sarbajna, V.H. Gessner, Acc. Chem. Res. 2022, 55, 770.
[5] A. Sarbajna, V.S.V.S.N. Swamy, V.H. Gessner, Chem. Sci. 2021, 12, 2016
[6] M. Jörges+, F. Krischer+, V. H. Gessner, Science, 2022, 378, 1331.