Synthesis of a new class of azathia crown macrocycles containing two 1,2,4-triazole or two 1,3,4-thiadiazole rings as subunits
β Scribed by Naser Foroughifar; Akbar Mobinikhaledi; Sattar Ebrahimi; Hassan Moghanian; Mohammad Ali Bodaghi Fard; Mehdi Kalhor
- Book ID
- 104096098
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 291 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
4-Thiadiazole a b s t r a c t A series of new 1,2/1,3-bis[o-(N-methylidenamino-5-aryl-3-thiol-4H-1,2,4-triazole-4-yl)phenoxy]alkane derivatives 3a-d and bis[o-(N-methylidenamino-2-thiol-1,3,4-thiadiazole-5-yl)phenoxy]alkanes 6a-c were prepared by condensation of 4-amino-5-(aroyl)-4H-1,2,4-triazole-3-thiols 2a-b or 2-amino-5-mercapto-1,3,4-thiadiazole with bis-aldehydes 1a-c. Further reaction of compounds 3a-d and 6a-c with dibromoalkanes afforded the new macrocycles 5a-f and 8a-d. The cyclization does not
π SIMILAR VOLUMES
## Abstract Syntheses of 1,3β2,4βcalix[4]bisβcrown ethers (**1** and **2**) fixed in the 1,3βalternate conformation by 1,3β and 2,4βbridges made of two modified polyether chains each containing two 1,2βphenylene residues and one pyridine or anisyl unit are reported. The structures of compounds **1*