The Claisen-Johnson Rearrangement Route to 1,4-Dicarbonyl Compounds: Synthesis of Ethyl 4-Ethoxy-4-alkenoates as Masked 4-Oxo Esters-Reference-Cited by-同舟云学术

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The Claisen-Johnson Rearrangement Route to 1,4-Dicarbonyl Compounds: Synthesis of Ethyl 4-Ethoxy-4-alkenoates as Masked 4-Oxo Esters

Published:1992 Issue:03 Volume:1992 Page:217-219
ISSN:0936-5214
Container-title:Synlett
language:en
Short-container-title:Synlett

Author:

Bao Rong,Valverde Serafín,Herradón Bernardo

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthetic approaches to 1,4-dicarbonyl compounds;Nature Synthesis;2022-11-07

2. Secondary Products from Intramolecular Cycloadditions of Azidoalkyl Enol Ethers and Azidoalkyl Vinyl Bromides: 1-Azadienes, Their Reactions with Diphenylketene, and Radical Cyclizations To Form Bi- and Tricyclic Lactams;The Journal of Organic Chemistry;2019-09-23

3. Synthesis and structures of α-lithiated vinyl ethers;Tetrahedron;2018-08

4. Rearrangements in Carbohydrate Templates to the Way to Peptide-Scaffold Hybrids and Functionalized Heterocycles;Domino and Intramolecular Rearrangement Reactions as Advanced Synthetic Methods in Glycoscience;2016-01-22

5. 1-Ethoxyvinyllithium;Encyclopedia of Reagents for Organic Synthesis;2011-03-15

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