The acid-catalysed dimerisation of the indenes (1)–(5), has been studied and a number of products isolated. The structure and stereochemistry of these compounds has been established by the use of crossed dimers, 13C-labelling, and 1H and 13C n.m.r. spectroscopy.
B. R. Davis, S. J. Johnson and P. D. Woodgate, J. Chem. Soc., Perkin Trans. 1, 1985, 2545 DOI: 10.1039/P19850002545
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...