Issue 2, 1990

2-Methyl-4,5-dihydroimidazole as a doubly nucleophilic unit: preparation of dihydroimidazole azaprostanoids

Abstract

2-Methyl-4,5-dihydroimidazole is incorporated as a doubly nucleophilic synthon, by successive alkylations at N-1 and C-2(Me), into monocyclic 9,12- and 8,11-diazaprostanoids containing the dihydroimidazole moiety. 2-Methyl-3a,4,7,7a-tetrahydrobenzimidazole is prepared (from 1,2,3,6-tetrahydrophthalic anhydride) and elaborated in the same way into a diazaprostacyclin precursor.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 375-383

2-Methyl-4,5-dihydroimidazole as a doubly nucleophilic unit: preparation of dihydroimidazole azaprostanoids

R. C. F. Jones and J. Schofield, J. Chem. Soc., Perkin Trans. 1, 1990, 375 DOI: 10.1039/P19900000375

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