The Stobbe Condensation with Substituted Succinic Esters. Part III. A Synthesis of Benzofuran and Indole Derivatives
Author:
Publisher
Wiley
Subject
Environmental Engineering
Reference12 articles.
1. The STOBBE condensation. X. The cyclisation of (E)-3-methoxycarbonyl-4-(5?-methyl-2?-furyl)-but-3-enoic acid, and (E)?3-methoxycarbonyl-4-(2?-furyl)-pent-3-enoic acid, to Benzofuran Derivatives
2. The STOBBE Condensation with Pyrrolyl Aldehydes - a synthesis of indole derivatives
3. The Stobbe Condensation with Sodium Hydride1
4. The Stobbe Condensation with 2-Acetylnaphthalene. A Synthesis of 2,4-Dimethylphenanthrene
5. The STOBBE condensation with substituted succinic esters, part I. A Synthesis of Benzothiophene Derivatives
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3. Recent Advances in the Benzannulation of Substituted 3-Alkoxycarbonyl-3,5-hexadienoic Acids and 3-Alkoxycarbonylhex-3-en-5-ynoic Acids to Polysubstituted Aromatics;Chemistry - A European Journal;2007-08-17
4. A Reinvestigation of 4-Hydroxyindole-6-carboxylate Synthesis from Pyrrole-2-carboxaldehyde: A Facile Synthesis of Indoles and Indolizines;The Journal of Organic Chemistry;2004-09-09
5. The Stobbe condensation. Part 5. Reactions of aryl aldehydes with .alpha.,.alpha.-disubstituted succinic esters;Journal of Chemical & Engineering Data;1986-07
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