Aromatic ring synthesis by 1,3-Michael-Claisen annulation: Formation of dihydrobenzofurans and tetrahydrochromans from α-methylene γ-butyrolactone and δ-valerolactone-Reference-Cited by-同舟云学术

Aromatic ring synthesis by 1,3-Michael-Claisen annulation: Formation of dihydrobenzofurans and tetrahydrochromans from α-methylene γ-butyrolactone and δ-valerolactone

Published:1995-08 Issue:35 Volume:51 Page:9559-9568
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Solladié Guy,Boeffel Dominique,Maignan Jean

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. A general highly efficient access to prenylated phenolic natural products. Synthesis of colletochlorins B and D

2. Aromatic annelation with .ALPHA.-phenylsulfinyl-.GAMMA.-butyrolactones. A novel route to 4-(2-hydroxyalkyl)-1,3-benzenediols.

3. Annulation reactions leading to naphthalene derivatives. New syntheses of natural 1,2- and 1,4-naphthoquinones

4. Regiospecific total synthesis of juncusol

5. Construction of Highly Substituted Nitroaromatic Systems by Cyclocondensation. Part II. Conversion of 4-nitro-3-oxobutyrate to 3-nitrosalicylates

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3. A Streamlined Synthesis of 2,3-Dihydrobenzofuransviatheortho-Quinone Methides Generated from 2-Alkyl-Substituted Phenols;Advanced Synthesis & Catalysis;2014-01-22

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5. Multicomponent Cascade Reactions for the Synthesis of 2,3-Dihydrobenzofuran Derivatives;Chemistry Letters;2012-12-05