Ireland-Claisen rearrangement of substrates bearing chiral enol ether units
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference33 articles.
1. A New Antibiotic. Furanomycin, an Isoleucine Antagonist
2. Nonprotein amino acid furanomycin, unlike isoleucine in chemical structure, is charged to isoleucine tRNA by isoleucyl-tRNA synthetase and incorporated into protein.
3. A short route to N-protected furanomycin, 5′-epi-furanomycin and isofuranomycin derivatives
4. Synthesis ofL-Furanomycin and Its Analogues via Furoisoxazolines
5. A General Approach toL-(+)-Furanomycin and Some Stereoisomers and Analogues Using Furoisoxazoline Intermediates
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1. [3,3]-Sigmatropic rearrangements: a variety of methods and recent advances;Russian Chemical Reviews;2022
2. 32.5.3.2 Enol Ethers (Update 2017);Knowledge Updates: 2017/3;2017
3. Recent applications in natural product synthesis of dihydrofuran and -pyran formation by ring-closing alkene metathesis;Organic & Biomolecular Chemistry;2016
4. Stereoselective Pd-catalyzed etherification and asymmetric synthesis of furanomycin and its analogues from a chiral aziridine;Organic & Biomolecular Chemistry;2015
5. A Versatile Approach to Noncoded β-Hydroxy-α-amino Esters and α-Amino Acids/Esters from Morita–Baylis–Hillman Adducts;Synthesis;2014-10-02
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