Synthesis and x-ray study of novel azofurazan-annulated macrocyclic lactams
โ Scribed by Aleksei B. Sheremetev; Nataliya S. Aleksandrova; Dmitrii E. Dmitriev; Boris B. Averkiev; Mikhail Yu. Antipin
- Book ID
- 102343926
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 93 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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โฆ Synopsis
Reaction of 1,4-di-(3-aminofurazan-4-oyl)piperazine 4 with dibromoisocyanurate (DBI) affords azofurazan-annulated macrocyclic lactam 7; the X-ray structure of the macrocycle 7 is reported. The synthesis was started with 3-aminofurazan-4-carboxylic acid 1. A one-pot method for preparation of the amino acid was elaborated from commercially available cyanoacetic ester. Amides of the acid have been prepared via the esterification and subsequent amination.
๐ SIMILAR VOLUMES
tetrathiacyclooctadecane (3) have been obtained by intermolecular cyclization of 1,3-bis(2-bromoethyl)adamantane (4) with thioacetamide using a high-dilution technique. The reaction is concentration-dependent. The crystal structures of 1, 2, and 3 have been determined by single-crystal X-ray diffra