The aryltetralins 7a and 7b and the keto-lactone 8 are synthesised by cyclisation and deprotection of the conjugate addition products 4a and 4b; the structure of 7b was unambiguously confirmed by an X-ray structural analysis.
R. S. Ward, A. Pelter, A. Brizzi, A. Sega and P. Paoli, J. Chem. Res. (S), 1998, 226 DOI: 10.1039/A704399F
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...