Ireland-Claisen rearrangement of secondary allyl acetate revisited: inevitable C-silylation circumvented by one-pot application of excessive LDA/TMSCl and TBAF-Reference-Cited by-同舟云学术

Ireland-Claisen rearrangement of secondary allyl acetate revisited: inevitable C-silylation circumvented by one-pot application of excessive LDA/TMSCl and TBAF

Published:2012-04 Issue:17 Volume:53 Page:2177-2180
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Liu Di,Yu Xiaoming

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

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5. Improved Synthesis of the Pheromone of the Longtailed Mealybug

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1. Copper-Catalyzed Reductive Ireland–Claisen Rearrangements of Propargylic Acrylates and Allylic Allenoates;The Journal of Organic Chemistry;2021-12-17

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3. Why do thioureas and squaramides slow down the Ireland–Claisen rearrangement?;Beilstein Journal of Organic Chemistry;2019-12-10

4. Tandem Copper-Catalyzed Conjugate Addition-Diastereoselective Protonation of (E)-α-Trialkylsilyl-β-Alkyl(Aryl)-α,β-Unsaturated Esters;Organic Letters;2018-09-14

5. Synthesis of substituted allyl acetates from heterocyclic dienes by Pd-promoted arylation-acetoxylation cascade;Journal of the Serbian Chemical Society;2017