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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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