Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/138714
Title: Rhodium-catalyzed arylzincation of alkynes : ligand control of 1,4-migration selectivity
Authors: Ming, Jialin
Hayashi, Tamio
Keywords: Science::Chemistry
Issue Date: 2018
Source: Ming, J., & Hayashi, T. (2018). Rhodium-catalyzed arylzincation of alkynes : ligand control of 1,4-migration selectivity. Organic Letters, 20(19), 6188-6192. doi:10.1021/acs.orglett.8b02668
Journal: Organic Letters
Abstract: The addition of arylzinc reagents ArZnCl 1 to alkynes 2 was found to be catalyzed by rhodium complexes in the presence of a catalytic amount of zinc chloride. The selectivity in giving 2-arylalkenylzinc species 3 or ortho-alkenylarylzinc species 4, the latter of which is generated through 1,4-Rh migration from alkenyl to aryl in the catalytic cycle, is controlled by the ligands on rhodium. Ligands cod and binap gave 3 and 4, respectively, with high selectivity.
URI: https://hdl.handle.net/10356/138714
ISSN: 1523-7060
DOI: 10.1021/acs.orglett.8b02668
Schools: School of Physical and Mathematical Sciences 
Rights: © 2018 American Chemical Society. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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