Iodocyclization/base-induced hydrodeiodination reaction of 5-substituted 4-alkenols. The influence of substituent on the stereoselective pathway
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference33 articles.
1. A highly efficient synthesis of 1,2,3,4-tetrahydroquinolines by molecular iodine-catalyzed domino reaction of anilines with cyclic enol ethers
2. InCl3-Catalyzed Domino Reaction of Aromatic Amines with Cyclic Enol Ethers in Water: A Highly Efficient Synthesis of New 1,2,3,4-Tetrahydroquinoline Derivatives
3. A General Synthesis of Substituted Indoles from Cyclic Enol Ethers and Enol Lactones
4. Heck arylation of cyclic enol ethers with aryldiazonium salts: regio- and stereoselective synthesis of arylated oxacycles
5. Catalytic Enantioselective Hetero Diels−Alder Reactions of α,β-Unsaturated Acyl Phosphonates with Enol Ethers
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1. iodocyclization;Catalysis from A to Z;2020-04-20
2. Facile iodination of the vinyl groups in protoporphyrin IX dimethyl ester and subsequent transformation of the iodinated moieties;Tetrahedron;2018-07
3. Eugenol as renewable comonomer compared to 4-penten-1-ol in ethylene copolymerization using a palladium aryl sulfonate catalyst;Polymer;2017-04
4. Tandem vinylcyclopropane ring opening/Prins cyclization for the synthesis of 2,3-disubstituted tetrahydropyrans;Tetrahedron Letters;2016-04
5. A convenient method for lactonization of α-allyl esters using iodine in dimethyl- sulphoxide;Bulletin of the Chemical Society of Ethiopia;2014-09-22
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