The π-allyi lanthanoid ate complex (1), which was prepared in situ from tetra-allyltin, the lanthanoid trichloride, and n-butyl-lithium in tetrahydrofuran (THF), reacts smoothly with α,β-unsaturated carbonyl compounds (3)–(11) with a high degree of 1,2-regioselectivity to give 3-hydroxy-1, 5-dienes (12)–(20) in good to excellent yields.
S. Fukuzawa, K. Sato, T. Fujinami and S. Sakai, J. Chem. Soc., Chem. Commun., 1990, 939 DOI: 10.1039/C39900000939
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...