Intramolecular cyclization of N, N-di (oligooxyethylene) amines: A new synthesis of monoaza crown ethers
H Maeda, S Furuyoshi, Y Nakatsuji, M Okahara
Index: Maeda, Hirokazu; Furuyoshi, Shigeo; Nakatsuji, Yohji; Okahara, Mitsuo Tetrahedron, 1982 , vol. 38, # 22 p. 3359 - 3362
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Citation Number: 13
Abstract
The reaction of N, N-di (oligooxyethylene) amines with arenesulfonyl chloride in the presence of alkali metal hydroxide was investigate. It was found that the monoarenesulfonates of N, N-di (oligooxyethylene) amines were first formed as intermediates, and their subsequent intramolecular cyclization gave N-unsubstituted monoaza crown ethers rather selectively.
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