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- W2801519263 abstract "An important and surprising finding that the acetalization and ketalization of aldehydes and ketones with alcohols, respectively, proceed smoothly in the presence of 0.1 mol % acid, without removing water, has been presented. This process has many merits, such as commercial available catalysts with low cost and low loadings (as low as 0.03 mol %), quite a broad substrate scope (including various aldehydes, ketones, acid-sensitive substrates, and diols), a wide range of reaction temperature (-60 to 50 °C), high yields, large-scale preparation, environmental friendliness, and simple work-up procedure. This new protocol has also been successfully applied to protect the important organic compounds, such as 1,3-diols, 1,2-diols, acid-sensitive substrates, glucose, and 1,3-dicarbonyl compounds." @default.
- W2801519263 created "2018-05-17" @default.
- W2801519263 creator A5041465085 @default.
- W2801519263 creator A5081876255 @default.
- W2801519263 creator A5082550852 @default.
- W2801519263 date "2018-05-07" @default.
- W2801519263 modified "2023-10-14" @default.
- W2801519263 title "A Simple and Versatile Method for the Formation of Acetals/Ketals Using Trace Conventional Acids" @default.
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- W2801519263 doi "https://doi.org/10.1021/acsomega.8b00159" @default.
- W2801519263 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6641695" @default.
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