l-Benzyl-2-(ethoxycarbonylmethylene)-2,3,4,5-tetrahydroimidazole undergoes preferred Calkylation with halogenoalkanes, dihalogenoalkanes and epoxides; subsequent removal of of the ethoxycarbonyl group provides a new route to 2-alkyl-4,5-dihydroimidazoles. 1.3-Dihalogenoalkanes afford imidazo[l,2-a]p
✦ LIBER ✦
ChemInform Abstract: Alkylation of an Imidazolidine Enaminoester: A New Sequence for the Cα-Alkylation of 4,5-Dihydroimidazoles.
✍ Scribed by R. C. F. JONES; P. PATEL; S. C. HIRST; I. TURNER
- Book ID
- 101860278
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 40 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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## 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
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