Issue 3, 1975
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Cyclisation reactions. Part III. Cyclisation of trans-2,3-epoxy-9-m-methoxyphenyl-2,6-dimethylnon-6-ene

Dhanonjoy Nasipuri  and  Swadesh R. Ray Chaudhuri  

Abstract

9-m-Methoxyphenyl-2,6-dimethylnona-2,6-diene (VI) has been converted into the 2,3-epoxide (VIII) and the latter cyclised to give (±)-13-methoxypodocarpa-8,11,13-trien-3β-ol (IX)(25%) as the major product. An alcohol and a ketone isolated in 12 and 17% yield respectively have been tentatively assigned as the 11-methoxy-isomer (X) and trans-3-(2-m-methoxyphenylethyl)-2,2,4-trimethylcyclohexanone (XII).

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/P19750000262
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 262-265

Permissions

Request permissions

Cyclisation reactions. Part III. Cyclisation of trans-2,3-epoxy-9-m-methoxyphenyl-2,6-dimethylnon-6-ene

D. Nasipuri and S. R. R. Chaudhuri, J. Chem. Soc., Perkin Trans. 1, 1975, 262 DOI: 10.1039/P19750000262

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