Water/MAO acceleration of the zirconocene-catalyzed asymmetric methylalumination of alpha-olefins

Authors
Citation
P. Wipf et S. Ribe, Water/MAO acceleration of the zirconocene-catalyzed asymmetric methylalumination of alpha-olefins, ORG LETT, 2(12), 2000, pp. 1713-1716
Citations number
20
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
2
Issue
12
Year of publication
2000
Pages
1713 - 1716
Database
ISI
SICI code
1523-7060(20000615)2:12<1713:WAOTZA>2.0.ZU;2-B
Abstract
[GRAPHICS] The zirconocene-catalyzed enantioselective methylalumination of terminal al kenes is greatly accelerated in the presence of water. Terminal olefins tha t are inert under the standard conditions can be readily methylated in good yields and with good to high enantioselectivities. Furthermore, methylalum inoxane is also shown to accelerate the reaction, albeit at a lesser rate.