Aqueous intermolecular diels-alder chemistry: novel products derived from substituted benzoquinone-diene carboxylate adducts via tandem Michael reactions-Reference-Cited by-同舟云学术

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Aqueous intermolecular diels-alder chemistry: novel products derived from substituted benzoquinone-diene carboxylate adducts via tandem Michael reactions

Published:1983-01 Issue:36 Volume:24 Page:3807-3810
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Grieco Paul A.,Garner Philip,Yoshida Kiyoshi,Huffman John C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference3 articles.

1. “Micellar” catalysis in the aqueous intermolecular diels-alder reaction: rate acceleration and enhanced selectivity

2. Selective diels-alder reactions in aqueous solutions and suspensions

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3. 2-Pyridyldimethylsilyl Group as a Removable Hydrophilic Group in Aqueous Organic Reactions: Formation of Molecular Aggregates and Dramatic Rate Enhancement in Diels-Alder Reactions;Advanced Synthesis & Catalyis;2002-06

4. Salt Effects on Diels−Alder Reaction Kinetics;Chemical Reviews;2000-11-29

5. Catalytic oxidation of 2,6-dialkylphenols to the corresponding 2,6-dialkyl-1,4-benzoquinones by molecular oxygen in the presence of P–Mo–V heteropoly acids;Journal of Molecular Catalysis A: Chemical;2000-03

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