The synthesis of azahomotryptophane derivatives. The transformation of N-trifluoroacetyl-5-bromo-4-oxonorvaline methyl ester into 4-(imidazo[1,2-a]azinyl-3)-4-oxohomoalanine derivatives
✍ Scribed by Marko Škof; Jurij Svete; Branko Stanovnik
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 274 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
Azatryptophane homologues, 4‐(imidazo[1,2‐a]pyridinyl‐3)‐ 9a‐9f and 4‐(imidazo[1,2‐a]pyrimidinyl‐3)‐4‐oxohomoalanine derivatives 9g‐91, were prepared from N,N‐dimethyl‐N′‐(pyridinyl‐2)‐ 6a‐6f and N,N‐dimethyl‐N‐(pyriniidinyl‐2)formamidines 6g‐6i, and (S)‐N‐trifluoroacetyl‐5‐bromo‐4‐oxonorvaline methyl ester (2) and its (R,S)‐isomer.
📜 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 “Full Text” option. The original article is trackable v
## Abstract 4‐(2‐Bromo‐1‐dimethylaminoethylidene)‐2‐phenyl‐5(4__H__)‐oxazolone (5) reacts with __N,N__‐dimethyl‐__N'‐__heteroarylformamidines 7 to form imidazoazine derivatives 9 with the oxazolone ring connected through a conjugated double bond to the fused imidazole system at position 3. Compound