O-Alkylation of cyclic thiohydroxamic acids 1 and 3-5 has large countercations, such as M = NBu 4 , are treated with hard alkylating reagents in polar aprotic media. (iv) As been studied with a view to developing an efficient method for the synthesis of N-(alkoxy)pyridine-2(1H)-thiones and N-tetrabu
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ChemInform Abstract: Selective O-Alkylation of Ambident Nucleophiles — The Synthesis of Thiohydroxamic Acid O-Esters by Phase-Transfer Reactions.
✍ Scribed by Jens Hartung; Rainer Kneuer; Michaela Schwarz; Ingrid Svoboda; Hartmut Fuess
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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