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Journal ArticleDOI

Organoaluminium assisted rearrangements of five-membered ring enol ethers with vinyl substituents

Ichiro Mori, +3 more
- 01 Jan 1984 - 
- Vol. 40, Iss: 20, pp 4013-4018
TLDR
In this article, organoaluminium reagents such as i Bu 3 A1, PhC=CA1Et 2, and Et 2 A1SPh mediate the title reactions in three different directions.
About
This article is published in Tetrahedron.The article was published on 1984-01-01. It has received 22 citations till now. The article focuses on the topics: Sigmatropic reaction & Enol ether.

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Citations
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Journal ArticleDOI

Rare-earth metal triflates in organic synthesis

TL;DR: The main findings are: Lanthanide(II) Triflates in Organic Synthesis inorganic Synthesis 2295 10.2.1.
Journal ArticleDOI

The (4+3)-cycloaddition reaction: simple allylic cations as dienophiles

TL;DR: The (4+3)-cycloaddition of allylic cations to dienes is a powerful method for the direct synthesis of seven-membered rings and applications to the total synthesis of natural products and their analogues.
Book ChapterDOI

7.2 – Claisen Rearrangements

TL;DR: In this paper, a survey of variants of the Claisen rearrangement that are of general use in stereoselective organic synthesis is presented, highlighting the influence of steric and electronic parameters on transition state geometries.
Journal ArticleDOI

Development of a New Lewis Acid-Catalyzed Claisen Rearrangement

TL;DR: In this paper, the authors describe a broadly useful Lewis acid-catalyzed [3, 3]-sigmatropic rearrangement that they expect will provide a new avenue for the development of an enantioselective catalytic Claisen process.
References
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Journal ArticleDOI

Transition-metal catalyzed silylmetalation of allenes

TL;DR: In the presence of various transition-metal catalysts, a 3-dimethylphenylsilyl-1-cyclononene with high degrees of regioselectivity can be obtained as discussed by the authors.
Journal ArticleDOI

Aliphatic claisen rearrangement promoted by organoaluminium compounds

TL;DR: In this article, allyl vinyl ether derivatives with organoaluminiumamphoteric reagent, R 3 Al or R 2 AlSPn, results in the title reaction at room temperature under uptake of R, H or SPh as a nucleophile on the aldehydic carbon.
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