期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2018, 期 25, 页码 3326-3335出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201800737
关键词
Polycycles; Fused-ring systems; Photochemistry; Cyclization; Oxygen heterocycles; Nitrogen heterocycles
Promising test results on the biological activity of our previously described naphtho[1,2-d]oxazoles and heterobenz[1,2-d]oxazoles, obtained by the photochemical cyclization of 5-phenylethenyl- and 5-heteroarylethenyloxazoles, prompted us to continue with the photochemical synthesis of substituted naphtho[1,2-d]oxazoles, and to extend the photochemical cyclization to the synthesis of naphtho/heterobenz[2,1-d]oxazoles from 4-(aryl/heteroarylethenyl)oxazoles. The required p- and o-phenyl-substituted 5-arylethenyloxazoles were prepared from the corresponding ,-unsaturated aldehydes and the TosMIC reagent (tosylmethyl isocyanide) by the Van Leusen reaction. The substituted 4-(aryl/heteroarylethenyl)oxazoles were prepared by the Wittig reaction starting from various phosphonium salts and 2-H/methyl-4-oxazolecarbaldehydes.
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