Yanphos-Catalyzed Asymmetric Interrupted

Mar 10, 2017 - Huo, Sun, Yan, Song, Zhang, Xie, Liu, Ji, Jiang, Zhou, and Zeng. 2017 139 (9), pp 3568–3568. Abstract | Full Text HTML | PDF w/ Links...
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Addition/Correction pubs.acs.org/JACS

Correction to “Rhodium/Yanphos-Catalyzed Asymmetric Interrupted Intramolecular Hydroaminomethylation of trans-1,2-Disubstituted Alkenes” Caiyou Chen, Shicheng Jin, Zhefan Zhang, Biao Wei, Heng Wang, Kai Zhang, Hui Lv,* Xiu-Qin Dong,* and Xumu Zhang* J. Am. Chem. Soc. 2016, 138, 9017−9020. DOI: 10.1021/jacs.6b03596 S Supporting Information *

Scheme 4. Synthetic Transformations

Page 9019. In Table 3, the stereochemistry of 4o was assigned incorrectly. The corrected Table 3 is given here. Page 9020. In Scheme 4, the structure of compound 7 was drawn incorrectly. The corrected Scheme 4 is given here. Table 3. Substrate Scope of the Preparation of Chiral Pyrrolidines through the Interrupted Asymmetric HAMa

The stereochemistry of 4o and the structure of 7 were also misassigned in the Supporting Information, and the calculated HRMS data were misread as the obtained data in the HRMS report. The Supporting Information has been updated and is given here.



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S Supporting Information *

The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/jacs.6b13274. Procedures and characterization data (corrected) (PDF) a

The reaction was conducted on a 0.1 mmol scale in 0.5 mL of toluene, Rh(acac)(CO)2 as the metal precursor, (S,R)-(N-Bn)Yanphos as the ligand, CO:H2 = 10:10 bar, S/C = 20, HSiEt3 (0.3 mmol), and BF3.Et2O (0.3 mmol) The configuration of all of the products was determined to be S, except for 4m; only the desired regioisomer was obtained as determined by NMR analysis. © XXXX American Chemical Society

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DOI: 10.1021/jacs.6b13274 J. Am. Chem. Soc. XXXX, XXX, XXX−XXX