Issue 17, 1999
From the journal:

Chemical Communications

Stereoselective total synthesis of (±)-fragranol by TiCl4 promoted [2+2] cycloaddition of allyl-tert-butyldiphenylsilane and methyl methacrylate†

Hans-Joachim Knölker,   Oliver Schmitt,   Günter Wanzl  and  Gerhard Baum  

Abstract

A stereoselective total synthesis of the monoterpenoid alcohol (±)-fragranol has been accomplished utilizing a TiCl4 promoted [2 + 2] cycloaddition of allyl-tert-butyldiphenylsilane and methyl methacrylate as the key step.

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/A905019A
Article type
Paper

Chem. Commun., 1999, 1737-1738

Permissions

Request permissions

Stereoselective total synthesis of (±)-fragranol by TiCl4 promoted [2+2] cycloaddition of allyl-tert-butyldiphenylsilane and methyl methacrylate†

H. Knölker, O. Schmitt, G. Wanzl and G. Baum, Chem. Commun., 1999, 1737 DOI: 10.1039/A905019A

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.

Social activity

Spotlight

Advertisements