A Novel Propargylation/Cycloisomerization Tandem Process Catalyzed by a Ruthenium(II)/Trifluoroacetic Acid System: One-Pot Entry to Fully Substituted Furans from Readily Available Secondary Propargylic Alcohols and 1,3-Dicarbonyl Compounds-Reference-Cited by-同舟云学术

A Novel Propargylation/Cycloisomerization Tandem Process Catalyzed by a Ruthenium(II)/Trifluoroacetic Acid System: One-Pot Entry to Fully Substituted Furans from Readily Available Secondary Propargylic Alcohols and 1,3-Dicarbonyl Compounds

Published:2007-02-05 Issue:3 Volume:349 Page:382-394
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Cadierno Victorio,Gimeno José,Nebra Noel

Publisher

Wiley

Subject

General Chemistry

Reference83 articles.

1. Dichloro(dodeca-2,6,10-triene-1,12-diyl)ruthenium(iv): a highly efficient catalyst for the isomerization of allylic alcohols into carbonyl compounds in organic and aqueous media

2. Water-soluble ruthenium(ii) catalysts [RuCl2(η6-arene){P(CH2OH)3}] for isomerization of allylic alcohols and alkyne hydration

3. Catalytic Isomerization of Allylic Alcohols by (η6-p-Cymene)- Ruthenium(II) Complexes in Organic and Aqueous Media: New Recyclable and Highly Efficient Catalysts in Water Containing Ammonium-Functionalized Ligands

4. Bis(allyl)−Ruthenium(IV) Complexes as Highly Efficient Catalysts for the Redox Isomerization of Allylic Alcohols into Carbonyl Compounds in Organic and Aqueous Media: Scope, Limitations, and Theoretical Analysis of the Mechanism

5. Ru(iv)-catalyzed isomerization of allylamines in water: A highly efficient procedure for the deprotection of N-allylic amines

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