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Highly Z-Selective Metathesis Homocoupling of Terminal Olefins

Author(s)
Jiang, Annie J.; Zhao, Yu; Hoveyda, Amir H.; Schrock, Richard Royce
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Abstract
Mo and W MonoAryloxide-Pyrrolide (MAP) olefin metathesis catalysts can couple terminal olefins to give as high as >98% Z-products in moderate to high yields with as little as 0.2% catalyst. Results are reported for 1-hexene, 1-octene, allylbenzene, allyltrimethylsilane, methyl-10-undecenoate, methyl-9-decenoate, allylB(pinacolate), allylOBenzyl, allylNHTosyl, and allylNHPh. It is proposed that high Z-selectivity is achieved because a large aryloxide only allows metallacyclobutanes to form that contain adjacent cis substituents and because isomerization of Z-product to E-product can be slow in that same steric environment.
Date issued
2009-10
URI
http://hdl.handle.net/1721.1/82550
Department
Massachusetts Institute of Technology. Department of Chemistry
Journal
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Citation
Jiang, Annie J., Yu Zhao, Richard R. Schrock, and Amir H. Hoveyda. “Highly Z-Selective Metathesis Homocoupling of Terminal Olefins.” Journal of the American Chemical Society 131, no. 46 (November 25, 2009): 16630-16631.
Version: Author's final manuscript
ISSN
0002-7863
1520-5126

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