Asymmetric Organocatalytic Diels-Alder Reactions on Solid Support

Selkälä, S.A.; Tois, J.; Pihko, P.M.; Koskinen, A.M.P.

Aaltodoc
→
6b Artikkelit / Articles from Research information portal
→
[article-cris] Kemian tekniikan korkeakoulu / CHEM
→
View Item

Asymmetric Organocatalytic Diels-Alder Reactions on Solid Support

Altmetrics



Title:	Asymmetric Organocatalytic Diels-Alder Reactions on Solid Support
Author(s):	Selkälä, S.A. ; Tois, J. ; Pihko, P.M. ; Koskinen, A.M.P.
Date:	2002
Language:	en
Pages:	941-945
Department:	Department of Chemistry
Series:	ADVANCED SYNTHESIS AND CATALYSIS, Volume 344
ISSN:	1615-4150
DOI-number:	10.1002/1615-4169(200210)344:9<941::AID-ADSC941>3.0.CO;2-M
Keywords:	asymmetric synthesis, catalysis, organic chemistry, cycloaddition, organocatalysis, solid-phase catalysis
» Show full item record
This publication is imported from Aalto University Research information portal: https://research.aalto.fi > View this publication in Research information portal > View/Open full text file from Research information portal
Citation: Selkälä , S A , Tois , J , Pihko , P M & Koskinen , A M P 2002 , ' Asymmetric Organocatalytic Diels-Alder Reactions on Solid Support ' ADVANCED SYNTHESIS AND CATALYSIS , vol 344 , pp. 941-945 . DOI: 10.1002/1615-4169(200210)344:9<941::AID-ADSC941>3.0.CO;2-M
Abstract: Asymmetric organocatalysis on solid support combines the environmental advantages of metal-free catalysts and the ease of operation of solid-supported reagents. Enantioselective organocatalytic DielsAlder reactions have been demonstrated by two different solid-supported chiral organocatalysts. The catalysts are easy to recover and they can be reused. The reactivity of the catalyst can be tuned by changing the solid support.

Permanent link to this item: http://urn.fi/URN:NBN:fi:aalto-201609234431 Email this Export to RefWorks QR Code Print BibTex Tweet