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
“…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, aer 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.…”
An efficient organocatalytic method for the synthesis of new substituted 9-arylxanthenes (2a–2u) starting from diarylcarbinol compounds with an arenoxy group (1a–1u) has been developed using the intramolecular Friedel–Crafts reaction.
“…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, aer 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.…”
An efficient organocatalytic method for the synthesis of new substituted 9-arylxanthenes (2a–2u) starting from diarylcarbinol compounds with an arenoxy group (1a–1u) has been developed using the intramolecular Friedel–Crafts reaction.
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