Formal synthesis of (−)-anisomycin based on stereoselective nucleophilic substitution along with 1,2-aryl migration
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Formal total synthesis of (−)-anisomycin based on the stereoselective nucleophilic substitution along with aryl migration
2. Novel lactonization induced by the phenonium ion
3. Intramolecular Reaction of a Phenonium Ion. Novel Lactonization of 4-Aryl-5-tosyloxypentanoates and 4-Aryl-5-tosyloxyhexanoates Concomitant with a Phenyl Rearrangement1
4. Formal Total Synthesis of Enantiopure (−)-Anisomycin, Antibiotic from Streptomyces
5. A Facile Synthesis of 4-Aryl-5-hydroxy-(2E)-pentenoate Derivatives and Its Applications to the First Synthesis of (±)-Curucudiol, (±)-Curcuhydroquinone and (±)-Curcuquinone
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1. Oxidative Rearrangement via 1,2-Aryl Migration using Hydroxy(tosyloxy)iodobenzene in a Polar Aprotic Solvent;Synlett;2020-03-27
2. Studies Towards the Synthesis of (+)- and (–)-Anisomycin and Their Analogues;Synthesis;2017-10-04
3. Osmium Tetroxide;Encyclopedia of Reagents for Organic Synthesis;2013-04-22
4. Enantioselective Copper-Catalysed Propargylic Substitution: Synthetic Scope Study and Application in Formal Total Syntheses of (+)-Anisomycin and (−)-Cytoxazone;Chemistry - A European Journal;2011-04-15
5. Application of the PIFA–mediated alkyne amidation reaction to the formal synthesis of (±)-clausenamide;Arkivoc;2009-04-03
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