Synthesis of Ring-Halogenated Histidines and Histamines. -Histamines (or the corresponding histidine methyl esters) are halogenated predominantly in 5 position leading to monohalo compounds (III), which may be used for the preparation of mixed dihalo derivatives, such as (IV). 2-Halo derivatives ar
Synthesis of ring-halogenated histidines and histamines
β Scribed by Rahul Jain; Bianca Avramovitch; Louis A. Cohen
- Book ID
- 104208459
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 733 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
Series of ring-halogenated histidines and histamines have been synthesized horn the suitably protected parent bioimidazoles. The 5-X and 2,5-X*-derivatives are obtained by dii electrophilic halogenation while 2-X derivatives (X= Br and I) are prepared by rcgiospecific electrophilic dehalogenation at C-5.
π SIMILAR VOLUMES
Synthesis of novel 2-cycloall,~vI-L-histidines and 2-cycloall, ylhistamines via radical alkylation with cycloall~ylcarbo~lic acids and sih,er nitrate in the presence of 10% H:SOΒ’ by ammonium persulfate is described. The method is also extended to the synthesis of 1,2-diall~TI-L-histidines and 1,2-di