1987
DOI: 10.1021/jo00233a034
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Lactone formation in the oxidation of diols with N-iodosuccinimide and silver acetate

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Cited by 14 publications
(4 citation statements)
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“…Lactones can be synthesized by dehydrogenation or oxidation of the corresponding α,ω-diols and cyclic ketones (Scheme ). Current methods for the synthesis of lactones involve the use of strong reaction conditions and oxidants , or the sacrifice of a series of cooxidants such as aldehydes and N-oxides.…”
Section: Multistep Sequential Processesmentioning
confidence: 99%
“…Lactones can be synthesized by dehydrogenation or oxidation of the corresponding α,ω-diols and cyclic ketones (Scheme ). Current methods for the synthesis of lactones involve the use of strong reaction conditions and oxidants , or the sacrifice of a series of cooxidants such as aldehydes and N-oxides.…”
Section: Multistep Sequential Processesmentioning
confidence: 99%
“…They can be synthesized by dehydrogenation or oxidation of the corresponding α,ω-diols and cycloketones. Current synthesis procedures involve with fierce reaction conditions and oxidants, , or the sacrifice of a series of cooxidants such as aldehydes, , N -oxide, and so forth. Abundant wastes are generated, and the process is not in accordance with the requirements of green chemistry and sustainable development.…”
Section: Introductionmentioning
confidence: 99%
“…Subsequent addition of 0.5 equivalents of 1,2‐bis(4‐pyridyl)ethane to the reaction mixture at ambient temperature resulted in slow deposition of colorless crystals of the novel carboxylate alumoxane 2 (path a, Scheme ). Interestingly, analysis of the reaction mixture confirmed the conversion of approximately half of an equivalent of phthalic acid into 3,3‐dimethyl‐2‐benzofuran‐1(3 H )‐one ( A ) 14. Thus, the additional equivalent of AlMe 3 leads to C‐alkylation of the carboxylate group with the concomitant formation of the cyclic ester A and tetramethylalumoxane, and the latter alumoxane species is subsequently trapped by unreacted 1 .…”
Section: Methodsmentioning
confidence: 98%