Literature DB >> 4414972

Ozonolysis of long-chain cyclic acetals: formation of monoesters.

W J Baumann, T H Madson.   

Abstract

A procedure is described for the quantitative conversion of saturated long-chain cyclic acetals of diols to the corresponding O-acyl diols. Acetal ozonolysis proceeds in ethyl acetate-methylene chloride solution at -16 to -18 degrees C without overoxidation.

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Year:  1974        PMID: 4414972

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  1 in total

1.  1-Docosanol and other long chain primary alcohols in developing rat brain.

Authors:  V Natarajan; H H Schmid
Journal:  Lipids       Date:  1977-01       Impact factor: 1.880

  1 in total

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