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13C and1H NMR spectra of biologically active compounds. VII. Diastereomers of 2,2-dialkylspiro[cyclopropane-3,3′-indene]-1-carboxylic acids of the pyrethroid series

✍ Scribed by L. M. Khalilov; V. S. Sultanova; E. V. Vasil'eva; L. V. Spirikhin; I. P. Baikova; S. N. Lakeev; F. Z. Galin; G. A. Tolstikov; A. A. Panasenko


Publisher
Springer
Year
1988
Tongue
English
Weight
477 KB
Volume
24
Category
Article
ISSN
0009-3130

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## Abstract The ^1^H and ^13^C NMR spectroscopic data for alkyl and polyamine‐linked bis(2‐thioxo‐[1,3,5]thiadiazinan‐3‐yl) carboxylic acids, prepared from alkyl diamines and __N__^4^‐(benzyl) spermidine have been fully assigned by combination of one‐ and two‐dimensional experiments (DEPT, HMBC, HM