## Abstract The^1^H and ^13^C NMR resonances for acridine derivatives 9‐substituted with chloro, allylamino and propargylamino groups were completely assigned using a concerted application of gs‐COSY, gs‐HMQC and gs‐HMBC experiments. 9‐(__N__‐Allyl)‐ and 9‐(__N__‐propargyl)acridinamine derivatives
1H and 13C chemical shifts for acridines: part XIX. N,N′-diacylproflavine derivatives
✍ Scribed by K. Shimi; G. Boyer; R. Faure; J.-P. Galy
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 80 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1701
No coin nor oath required. For personal study only.
✦ Synopsis
The 1 H and 13 C NMR resonances of 15 N,N -diacylproflavines were assigned completely and unequivocally using a concerted application of one-and two-dimensional experiments (DEPT, gs-COSY, gs-HMQC and gs-HMBC).
📜 SIMILAR VOLUMES
The 1 H and 13 C NMR chemical shifts of 16 4,5disubstituted acridine derivatives and nine 4-substituted-5,5 0 (˛0 0 ,ω 00diaminoacyl)bisacridine derivatives are reported. Chemical shift assignments were established from 1D and gradient-enhanced 2D measurements.
## Abstract The ^1^H and ^13^C NMR resonances for 16 acridin‐9(10__H__)‐ones substituted with amino or (1,3‐benzothiazol‐2‐yl)amino groups were completely and unequivocally assigned by the concerted application of gs‐COSY, gs‐HMQC and gs‐HMBC experiments. Evidence for hydrogen bond and amino–imino
## Abstract The ^1^H and ^13^C NMR resonances for forty‐three 2‐aryl and 2‐__N__‐arylamino benzothiazole derivatives were completely assigned using a concerted application of one‐ and two‐dimensional experiments (DEPT, gs‐COSY, gs‐HMQC and gs‐HMBC). Copyright © 2005 John Wiley & Sons, Ltd.
## Abstract The ^1^H and ^13^C NMR resonances for 18 tetracyclic acridines 9‐substituted on the acridine ring with Cl, NH~2~ and AMS [__N__‐(4‐amino‐3‐methoxyphenyl)1methanesulfonamide] groups were completely and unequivocally assigned by the concerted application of gs‐HMQC and gs‐HMBC experiments
## Abstract The ^13^C chemical shifts and some ^1^H^13^C coupling constants of twelve __N__‐arylpyrazoles are reported. The assignments were made by using the effects of a fluorine substituent and two‐dimensional techniques.