Literature DB >> 186202

Homologous synthesis: a method for the preparation of mixed substrates and individual compounds.

H K Mangold, H Becker, U Cramer, F Spener.   

Abstract

Equimolar mixtures of several homologous or vinylogous alkyl methanesulfonates (mesylates) are converted, by a series of reactions, into equimolar mixtures of compounds having one methylene group more, per molecule, than the starting material. Such mixtures can be used for studying the specificity of an enzymatic reaction in a single experiment in vivo or in vitro. The simultaneous synthesis of a mixture of compounds is also of great advantage in the preparation of a series of radioactively labelled substances. It is more convenient and much more efficient to prepare several labelled compounds of a homologous or vinylogous series in a single reaction, and to isolate each of them by chromatographic methods, than to synthesize the individual substances separately.

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Year:  1976        PMID: 186202     DOI: 10.1016/0009-3084(76)90061-x

Source DB:  PubMed          Journal:  Chem Phys Lipids        ISSN: 0009-3084            Impact factor:   3.329


  3 in total

1.  Formation of complex ether lipids from 1-O-alkylglycerols in cell suspension cultures of rape.

Authors:  N Weber; H K Mangold
Journal:  Planta       Date:  1983-06       Impact factor: 4.116

2.  Biosynthesis of wax esters in tissues of Sinapis alba L. seeds.

Authors:  I Richter; K D Mukherjee; N Weber
Journal:  Planta       Date:  1981-04       Impact factor: 4.116

3.  Metabolism of long-chain alcohols in cell suspension cultures of soya and rape.

Authors:  N Weber; H K Mangold
Journal:  Planta       Date:  1982-08       Impact factor: 4.116

  3 in total

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