Aluminium triflate: a remarkable Lewis acid catalyst for the ring opening of epoxides by alcohols
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2005/OB/B508924G
Reference5 articles.
1. Bismuth triflate-catalyzed mild and efficient epoxide opening by aromatic amines under aqueous conditions
2. Mechanisms Of Epoxide Reactions
3. A facile and efficient method for the rearrangement of aryl-substituted epoxides to aldehydes and ketones using bismuth triflate
4. Yttrium triflate-catalyzed addition of lithium enolates to 1,2-epoxides. Efficient synthesis of γ-hydroxy ketones
5. Yb(OTf)3 catalyzed highly regioselective allylation of aromatic epoxides: an efficient route to bishomoallyl alcohols
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