Addition/Correction pubs.acs.org/OrgLett
Correction to Palladium-Catalyzed Carbonylative Sonogashira Coupling of Aryl Bromides Using Near Stoichiometric Carbon Monoxide Karoline T. Neumann, Simon R. Laursen, Anders T. Lindhardt,* Benny Bang-Andersen, and Troels Skrydstrup* Org. Lett. 2014, 16 (8), 2216−2219. DOI: 10.1021/ol5007289 S Supporting Information *
S
olvent peaks and in some cases minor impurities had been removed from the 1H and 13C NMR spectra reported for compounds 3, 5, 7, 9, 10, 12, 15, 18b, 23, 26b, 27, 29, 30b, and 31b. Original FIDs were located for compounds 3, 7, 9, 12, 15, 29, 30b, and 31b, and the spectra were reprocessed and have been replaced in the revised Supporting Information. For compounds 10, 18b, 23, and 26b, the reactions were rerun and the new spectra have been provided in the corrected Supporting Information. For compound 5, the wrong spectra were submitted in the original Supporting Information. The correct spectra are now included in the revised Supporting Information. For compound 27, the original FID was not located, and new spectra were obtained and are provided in the revised Supporting Information. The spectra editing did not affect any of the conclusions of the published paper. The corrected yields based on the revised spectra are as follows: 10 (87% yield), 18b (98% yield), 23 (90% yield), and 26b (95% yield).
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ASSOCIATED CONTENT
S Supporting Information *
File containing revised spectra. The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.orglett.5b01250.
Received: April 28, 2015
© XXXX American Chemical Society
A
DOI: 10.1021/acs.orglett.5b01250 Org. Lett. XXXX, XXX, XXX−XXX
Correction to Palladium-Catalyzed Carbonylative Sonogashira Coupling of Aryl Bromides Using Near Stoichiometric Carbon Monoxide Karoline T. Neumann, Simon R. Laursen, Anders T. Lindhardt,* Benny Bang-Andersen, and Troels Skrydstrup* Org. Lett. 2014, 16 (8), 2216−2219. DOI: 10.1021/ol5007289 S Supporting Information *
S
olvent peaks and in some cases minor impurities had been removed from the 1H and 13C NMR spectra reported for compounds 3, 5, 7, 9, 10, 12, 15, 18b, 23, 26b, 27, 29, 30b, and 31b. Original FIDs were located for compounds 3, 7, 9, 12, 15, 29, 30b, and 31b, and the spectra were reprocessed and have been replaced in the revised Supporting Information. For compounds 10, 18b, 23, and 26b, the reactions were rerun and the new spectra have been provided in the corrected Supporting Information. For compound 5, the wrong spectra were submitted in the original Supporting Information. The correct spectra are now included in the revised Supporting Information. For compound 27, the original FID was not located, and new spectra were obtained and are provided in the revised Supporting Information. The spectra editing did not affect any of the conclusions of the published paper. The corrected yields based on the revised spectra are as follows: 10 (87% yield), 18b (98% yield), 23 (90% yield), and 26b (95% yield).
■
ASSOCIATED CONTENT
S Supporting Information *
File containing revised spectra. The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.orglett.5b01250.
Received: April 28, 2015
© XXXX American Chemical Society
A
DOI: 10.1021/acs.orglett.5b01250 Org. Lett. XXXX, XXX, XXX−XXX
