2015
DOI: 10.1016/j.tetlet.2015.08.046
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Practical synthesis of 2,5-disubstituted 1,3-dioxolane-4-ones and highly diastereoselective cis-2,5-disubstituted 1,3-dioxolane-4-ones from α-hydroxy acids catalyzed by N-triflylphosphoramide

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Cited by 5 publications
(1 citation statement)
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“…A study on this subject includes the preparation of 1,3dioxolane-4-ones starting from a-hydroxy acids and aldehydes with the use of 3g. 25 Another example reports a transformation, which has merged the Ugi reaction and Houben-Hoesch cyclisation in the presence of 3g. 26 In that report, aer several Brønsted and Lewis acids were examined, they found that the acid-promoted reaction is effective in the synthesis of many 3aminoindole molecules using 3g with high yields and under mild conditions.…”
Section: Introductionmentioning
confidence: 99%
“…A study on this subject includes the preparation of 1,3dioxolane-4-ones starting from a-hydroxy acids and aldehydes with the use of 3g. 25 Another example reports a transformation, which has merged the Ugi reaction and Houben-Hoesch cyclisation in the presence of 3g. 26 In that report, aer several Brønsted and Lewis acids were examined, they found that the acid-promoted reaction is effective in the synthesis of many 3aminoindole molecules using 3g with high yields and under mild conditions.…”
Section: Introductionmentioning
confidence: 99%