Synthesis of benzofuranones related to diazonamide via an intramolecular Pummerer reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Isolation and structure determination of diazonamides A and B, unusual cytotoxic metabolites from the marine ascidian Diazona chinensis
2. Synthesis of heterocyclic natural products: Model studies towards diazonamide A
3. Studies towards the synthesis of diazonamide A. Unexpected formation of a 3,4-bridged indole
4. Synthetic Studies on Diazonamide A. Benzofuranone-Tyrosine and Indole-Oxazole Fragment Support Studies
5. Iminophosphorane-Mediated Synthesis of 3-(Oxazol-5-yl)indoles: Application to the Preparation of Pimprinine Type Alkaloids
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1. A metal-free approach to highly functionalized 3-substituted-3-arylbenzofuran-2(3H)-ones;New Journal of Chemistry;2022
2. Repurposing the Pummerer Rearrangement: Determination of Methionine Sulfoxides in Peptides;ChemBioChem;2019-10-25
3. Formal Total Synthesis of Diazonamide A by Indole Oxidative Rearrangement;Chemistry - A European Journal;2016-06-27
4. 6.17 Polonovski- and Pummerer-type Reactions and the Nef Reaction;Comprehensive Organic Synthesis II;2014
5. An Approach to the Bis-oxazole Macrocycle of Diazonamides;Organic Letters;2010-12-21
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