15N NMR spectroscopy of 3-substituted 5-trichloromethyl-1,2-dimethyl-1H-pyrazolium chlorides
β Scribed by Marcos A. P. Martins; Claudio M. P. Pereira; Adilson P. Sinhorin; Adriano Rosa; Nilo E. K. Zimmermann; Helio G. Bonacorso; Nilo Zanatta
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 103 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.987
No coin nor oath required. For personal study only.
β¦ Synopsis
15 N NMR data of a series of 3-alkyl[aryl] substituted 5-trichloromethyl-1,2-dimethyl-1H-pyrazolium chlorides (where the 3-substituents are H, Me, Et, n-Pr, n-Bu, n-Pe, n-Hex, (CH 2 ) 5 CO 2 Et, CH 2 Br, Ph and 4-Br-C 6 H 4 ), are reported. The 15 N substituent chemical shifts (SCS) parameters are determined and these data are compared with the 13 C SCS values and data obtained by MO calculations.
π SIMILAR VOLUMES
1-Aryl-4-carboxy-5-methyl-1,2,3-triazoles were prepared by the condensation of aryl azides with ethyl acetoacetate. The structures of these compounds were characterized by MS, IR and 1H and 13C NMR spectroscopy. The measured and calculated 13C chemical shifts of the aromatic carbons were compared.
## Abstract Substituted 2β(phenylamino)β5βphenylβ1,3,4βoxadiazoles were studied by ^15^N NMR spectroscopy. All signals were assigned on the basis of HMQC and HMBC experiments. Chemical shifts values were correlated with empirical Hammett parameters as well as with calculated electron densities and
## Abstract ^1^H, ^13^C and ^15^N NMR chemical shifts of 10 substituted pyrazolo[1,5β__a__]pyrimidines were assigned based on DQF ^1^H, ^1^H COSY, PFG ^1^H, ^13^C HMQC and PFG ^1^H,X (X = ^13^C and ^15^N) HMBC experiments and on literature data. Copyright Β© 2002 John Wiley & Sons, Ltd.