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An article Controlling the selectivity and efficiency of the hydrogen borrowing reaction by switching between rhodium and iridium catalysts WOS:000487514400010 published article about ALPHA-ALKYLATION; C-ALKYLATION; KETONES; ALCOHOLS; AMIDES; DEHYDROGENATION; NANOPALLADIUM; COMPLEXES; ESTERS in [Wang, Danfeng; McBurney, Roy T.; Pernik, Indrek; Messerle, Barbara A.] Macquarie Univ, Dept Mol Sci, N Ryde, NSW 2109, Australia in 2019.0, Cited 47.0. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7. Name: Chalcone

The catalytic alkylation of ketones with alcohols via the hydrogen borrowing methodology (HB) has the potential to be a highly efficient approach for forming new carbon-carbon bonds. However, this transformation can result in more than one product being formed. The work reported here utilises bidentate triazole-carbene ligated iridium and rhodium complexes as catalysts for the selective formation of alkylated ketone or alcohol products. Switching from an iridium centre to a rhodium centre in the complex resulted in significant changes in product selectivity. Other factors – base, base loading, solvent and reaction temperature – were also investigated to tune the selectivity further. The optimised conditions were used to demonstrate the scope of the reaction across 17 ketones and 14 alcohols containing a variety of functional groups. A series of mechanistic investigations were performed to probe the reasons behind the product selectivity, including kinetic and deuterium studies.

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Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com