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. Author manuscript; available in PMC: 2020 Mar 26.
Published in final edited form as: Angew Chem Int Ed Engl. 2019 Feb 27;58(14):4705–4709. doi: 10.1002/anie.201900545

Table 3.

Hydroacylation Scope with Styrenyl Olefins[a]

graphic file with name nihms-1018968-t0010.jpg
[a]

With 0.10 mmol of 3.

With 0.10 mmol of 3. Isolated yields are given. Diastereoselectivities were determined by 1H NMR analysis of the unpurified reaction mixture. Enantioselectivities (ee’s) were determined by chiral SFC analysis. (RP)-1-[(S)-tert-Butylphosphinoyl]-2-[(S)-1-(diphenylphosphino)ethyl]ferrocene (L4) is abbreviated as JoSPOphos.