1990
DOI: 10.1002/prac.19903320513
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Rndikalnaja telomerizacija. Hrsg. Frejdlina, R. Ch.; Velicko, F. K.; Zlotskij, S. S.; Rachmankulov, D. L; Terenter, A.B.; 287 S., 4 Abb., 69 Tab., 21,5 × 14,2 cm. Moskva: Chimija 1988. Pappe

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“…5-Acyl-1,3-dioxanes 1 can serve as initial products to synthesize compounds having such a structural moiety. Recently, we described the conversion of ketones 1 into 5-alkenyl-l,3dioxanes [3], and, with the help of photo-induced processes, into cyclopropanole derivatives, which are difficult to prepare by other synthetical routes [4]. The heterocyclic ketones 1 can easily be prepared in high yields by an acid catalyzed condensation between dialkyl or aryl alkyl ketones with formaldehyde [5].…”
mentioning
confidence: 99%
“…5-Acyl-1,3-dioxanes 1 can serve as initial products to synthesize compounds having such a structural moiety. Recently, we described the conversion of ketones 1 into 5-alkenyl-l,3dioxanes [3], and, with the help of photo-induced processes, into cyclopropanole derivatives, which are difficult to prepare by other synthetical routes [4]. The heterocyclic ketones 1 can easily be prepared in high yields by an acid catalyzed condensation between dialkyl or aryl alkyl ketones with formaldehyde [5].…”
mentioning
confidence: 99%