Issue 3, 2001
From the journal:

Chemical Communications

Modified guanidines as chiral superbases: the first example of asymmetric silylation of secondary alcohols

Toshio Isobe,a   Keiko Fukuda,a   Yukari Arakib  and  Tsutomu Ishikawa*b  

* Corresponding authors

a Central Research Laboratory, Shiratori Pharmaceutical Co. Ltd., 6-11-24 Tsudanuma, Narashino, Japan

b Faculty of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi, Inage, Japan

Abstract

Modified guanidines could effectively mediate asymmetric silylation of secondary alcohols as recyclable bases under simple and mild conditions.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B009173L
Article type
Communication
Submitted
15 Nov 2000
Accepted
13 Dec 2000
First published
18 Jan 2001

Chem. Commun., 2001, 243-244

Permissions

Request permissions

Modified guanidines as chiral superbases: the first example of asymmetric silylation of secondary alcohols

T. Isobe, K. Fukuda, Y. Araki and T. Ishikawa, Chem. Commun., 2001, 243 DOI: 10.1039/B009173L

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