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Preparation of dithioesters by ester interchange and the PMR spectral properties of these compounds by N.H. Leon; R.S. Asquith is a Chemistry article available to read on EtoBox.

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## ~bdrsct-Aromatic and alipbatic dithiccstera, many of them new, have been easily synthesized m exallent yields by the ester interchange reaction between carboxymethyl dithioeaters and mcrcaptans. PMR spectra of these dithioeaters and the corresponding oxygen analogues show that a strong anisotropic dcshielding effect is associated with the highly polarized thiocarbonyl group. Compounds with R = aromatic are red and those with R = aliphatic are yellow. Yields are of 85-91%. ' Measured in CDCl, at 100 MHz with TMS as internal standard. ' From m/e of parent peak in mass spectrum. ' R. Mayer, S. Scheithauer and D. Kunx, Chem Ber. 99.1393 (1966). ' Ref. 22. ' J. H. Wood and R. W. Best, 1. Am Chem. Sot. 59,1011(1937). ' Red needles, recrystallized from light petroleum (b.p. w). ' Ref. 24. ' Ref. 7. ' Ref. 13. ' Yellow oil, dec. on distillation.

Who reads Preparation of dithioesters by ester interchange and the PMR spectral properties of these compounds?

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Author
N.H. Leon; R.S. Asquith
Publisher
Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0040-4020)
Published
1970
Language
EN
Field
Chemistry (Physical Sciences)

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