Facile Ruthenium(IV)-Catalyzed Single and Double Allylation of Indole Compounds using Alcohols as Substrates: Aspects of Ruthenium(IV) Allyl Chemistry-Reference-Cited by-同舟云学术

Facile Ruthenium(IV)-Catalyzed Single and Double Allylation of Indole Compounds using Alcohols as Substrates: Aspects of Ruthenium(IV) Allyl Chemistry

Published:2008-07-17 Issue:15 Volume:27 Page:3796-3805
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Gruber Stefan¹,Zaitsev Alexey B.¹,Wörle Michael¹,Pregosin Paul S.¹,Veiros Luis F.²

Affiliation:

1. Laboratory of Inorganic Chemistry, ETHZ, Hönggerberg, CH-8093 Zürich, Switzerland

2. Centro de Química Estrutural, Complexo I, Instituto Superior Técnico, Av. Rovisco Pais 1, 1049-001 Lisbon, Portugal

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om800295z

Reference131 articles.

1. Ruthenium-Catalyzed Cycloisomerizations of Diynols

2. Ruthenium-Catalyzed Alkyne−Propargyl Alcohol Addition. An Asymmetric Total Synthesis of (+)-α-Kainic Acid

3. An Unusual Ruthenium-Catalyzed Dimerization of Propargyl Alcohols

4. Metal Vinylidenes and Allenylidenes in Catalysis: Applications in Anti-Markovnikov Additions to Terminal Alkynes and Alkene Metathesis

5. Homologation of Monoterpenoids into New Sesquiterpenoidsvia Tandem Isomerisation/Claisen Rearrangement Reactions with Three-Component Ruthenium Catalysts, and Ru(methallyl)2(COD) Revealed by High Throughput Screening Techniques

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