Volume 116, Issue 45 pp. 6303-6306
Zuschrift

Catalytic Asymmetric Mercuriocyclization of γ-Hydroxy-cis-Alkenes

Sung Ho Kang Prof. Dr.

Sung Ho Kang Prof. Dr.

Center for Molecular Design and Synthesis, Department of Chemistry, School of Molecular Science (BK21), Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea, Fax: (+82) 42-869-2810

Search for more papers by this author
Mihyong Kim Dr.

Mihyong Kim Dr.

Center for Molecular Design and Synthesis, Department of Chemistry, School of Molecular Science (BK21), Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea, Fax: (+82) 42-869-2810

Search for more papers by this author
Suk Youn Kang Dr.

Suk Youn Kang Dr.

Center for Molecular Design and Synthesis, Department of Chemistry, School of Molecular Science (BK21), Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea, Fax: (+82) 42-869-2810

Search for more papers by this author
First published: 17 November 2004
Citations: 3

This work was supported by CMDS and the Brain Korea 21 Project.

Graphical Abstract

2-Monosubstituierte Tetrahydrofurane 2 entstehen mit 73–95 % ee bei der katalytischen enantioselektiven Mercuriocyclisierung von γ-Hydroxy-(Z)-alkenen 1 mit Hg(OAc)2 in Gegenwart von HgII, das mit dem Bisoxazolin 3 komplexiert ist. Der chirale Komplex wurde aus Hg(tfa)2 (0.2 Äquiv.) und 3 (0.3 Äquiv.) hergestellt. Die MeOH-Menge hat einen großen Einfluss auf die Enantioselektivität.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.