Matches in DBpedia 2016-04 for { ?s ?p "Acylals in organic chemistry are a group of chemical compounds sharing a functional group with the general structure R-C(OOCR)2. Acylals can be obtained by reaction of aldehydes with acetic anhydride and a suitable catalyst for instance with sulfated zirconia at low temperatures when used as protective groups for aldehydes. High temperature exposure converts the acylal back to the aldehyde."@en }
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- Acylal abstract "Acylals in organic chemistry are a group of chemical compounds sharing a functional group with the general structure R-C(OOCR)2. Acylals can be obtained by reaction of aldehydes with acetic anhydride and a suitable catalyst for instance with sulfated zirconia at low temperatures when used as protective groups for aldehydes. High temperature exposure converts the acylal back to the aldehyde.".
- Q2506457 abstract "Acylals in organic chemistry are a group of chemical compounds sharing a functional group with the general structure R-C(OOCR)2. Acylals can be obtained by reaction of aldehydes with acetic anhydride and a suitable catalyst for instance with sulfated zirconia at low temperatures when used as protective groups for aldehydes. High temperature exposure converts the acylal back to the aldehyde.".
- Acylal comment "Acylals in organic chemistry are a group of chemical compounds sharing a functional group with the general structure R-C(OOCR)2. Acylals can be obtained by reaction of aldehydes with acetic anhydride and a suitable catalyst for instance with sulfated zirconia at low temperatures when used as protective groups for aldehydes. High temperature exposure converts the acylal back to the aldehyde.".
- Q2506457 comment "Acylals in organic chemistry are a group of chemical compounds sharing a functional group with the general structure R-C(OOCR)2. Acylals can be obtained by reaction of aldehydes with acetic anhydride and a suitable catalyst for instance with sulfated zirconia at low temperatures when used as protective groups for aldehydes. High temperature exposure converts the acylal back to the aldehyde.".