Deprotection of carbonyl croups by anodic oxidation of dithioacetals : A key step in the synthesis of α-diones, α-ketols and chiral synthons.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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4. Oxidative Hydrolysis of 1,3-Dithiane Derivatives to Carbonyl Compounds Using Lead Dioxide/Boron Trifluoride Etherate Reagents
5. Synthesis of the principal components of the sex attractant from male Ips confusus frass: 2-methyl-6-methylene-7-octen-4-ol, 2-methyl-6-methylene-2,7-octadien-4-ol, and (+)-cis-verbenol
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1. Facile electrochemical synthesis of silyl acetals: An air-stable precursor to formylsilane;Tetrahedron Letters;2022-08
2. Enzyme-catalysed regio- and enantioselective preparative scale synthesis of (S)-2-hydroxy alkanones;RSC Advances;2015
3. Protection for the Carbonyl Group;Greene's Protective Groups in Organic Synthesis;2014-08-11
4. Aldehyde-Functionalized Benzenediazonium Cation for Multiprobe Immobilization on Microelectrode Array Surfaces;Langmuir;2011-01-06
5. ChemInform Abstract: Deprotection of Carbonyl Groups by Anodic Oxidation of Dithioacetals: A Key Step in the Synthesis of α-Diones, α-Ketols, and Chiral Synthones.;ChemInform;2010-08-23
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