## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Synthesis of New Benzo-substituted Macrocyclic Ligands Containing Pyridine or Triazole as Subcyclic Units
β Scribed by Ahmed H.M Elwahy; Ashraf A Abbas
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 283 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The macrocyclic diamides 11-21, 42 and 43 were prepared by nucleophilic reaction of the bis phenols 22-29 with the appropriate dihalo compounds 2, 3, 40 and 41, respectively. The macrocyclic dithiodiamides 30-33 were obtained in good yields upon treatment of 11, 13, 15 and 17 with Lawesson's reagent. The macrocycles 61-63 were prepared by condensation of the bis(aldehyde) 37 with the appropriate bis(aminotriazoles) 50-54 to give the corresponding Schiff bases 56-60 followed by NaBH 4 reduction.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract Five novel pyridonoβ18βcrownβ6 (**10β14**) and two new benzyloxyβsubstituted pyridinoβ18βcrownβ6 (**15** and **16**) ligands have been prepared. By the catalytic hydrogenative removal of the benzyl group from the benzyloxy moiety at position 4 of the pyridine ring of **15** and **16**,