Issue 11, 1989

Studies on bifunctional annulating reagents: a combined annulation–ring cleavage approach to the synthesis of eight- and nine-membered rings

Abstract

Eight- and nine-membered rings are available by using a combined annulation–ring cleavage strategy which utilises the reaction of the stannane (1) or the allylsilane (7) with silylated enediois and ring opening of the thus formed bicyclic diols.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 2139-2140

Studies on bifunctional annulating reagents: a combined annulation–ring cleavage approach to the synthesis of eight- and nine-membered rings

T. V. Lee, F. S. Roden and J. R. Porter, J. Chem. Soc., Perkin Trans. 1, 1989, 2139 DOI: 10.1039/P19890002139

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.

Spotlight

Advertisements