Issue 1, 2003
From the journal:

Green Chemistry

Preparation of optically active cis-4-methylcyclohex-4-ene-1,2-dicarboximides by a combination of Diels–Alder reaction and complexation with optically active hosts and enantioselective Diels–Alder reaction in inclusion crystals in a water suspension medium

Hisakazu Miyamoto,*a   Taku Kimura,a   Naoki Daikawaa  and  Koichi Tanakaa  

* Corresponding authors

a Department of Applied Chemistry, Faculty of Engineering, Ehime University, Matsuyama, Ehime, Japan
E-mail: miyamoto@eng.ehime-u.ac.jp

Abstract

Optically active Diels–Alder adducts were prepared using a one-pot preparative method and enantioselective Diels–Alder reaction with optically active hosts in a water suspension medium.

Graphical abstract: Preparation of optically active cis-4-methylcyclohex-4-ene-1,2-dicarboximides by a combination of Diels–Alder reaction and complexation with optically active hosts and enantioselective Diels–Alder reaction in inclusion crystals in a water suspension medium

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B208921C
Article type
Paper
Submitted
12 Sep 2002
First published
28 Nov 2002

Green Chem., 2003,5, 57-59

Permissions

Request permissions

Preparation of optically active cis-4-methylcyclohex-4-ene-1,2-dicarboximides by a combination of Diels–Alder reaction and complexation with optically active hosts and enantioselective Diels–Alder reaction in inclusion crystals in a water suspension medium

H. Miyamoto, T. Kimura, N. Daikawa and K. Tanaka, Green Chem., 2003, 5, 57 DOI: 10.1039/B208921C

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