INTRAMOLECULAR CYCLIZATION OF N,N-Di(OLIGOOXYETHYLENE)AMINES: A NEW SYNTHESIS OF MONOAZA CROWN ETHERS

DOI: 10.1016/0040-4020(82)80119-1

Source and publish data:

Tetrahedron p. 3359 - 3362 (1982)

Update date:2022-08-03

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Authors:

Maeda, Hirokazu

Furuyoshi, Shigeo

Nakatsuji, Yohji

Okahara, Mitsuo

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Article abstract of DOI:10.1016/0040-4020(82)80119-1

The reaction of N,N-di(oligooxyethylene)amines with arenesulfonyl chloride in the presence of alkali metal hydroxide was investigated.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.

Full text of DOI:10.1016/0040-4020(82)80119-1

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