C3-Symmetric tripodal tetra-amines - preparation from chiral amino alcohols via aziridines

DOI: 10.1016/S0957-4166(97)00302-9

Source and publish data:

Tetrahedron Asymmetry p. 2655 - 2662 (1997)

Update date:2022-08-03

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Authors:

Cernerud, Magnus

Adolfsson, Hans

Moberg, Christina

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Article abstract of DOI:10.1016/S0957-4166(97)00302-9

Enantiopure N-sulfonylaziridines, conveniently obtained from readily available enantiopure amino alcohols, undergo smooth ring opening reactions using ammonia as a nucleophile to yield tripodal tetradentate C₃-symmetric amines. N-alkylation and

Full text of DOI:10.1016/S0957-4166(97)00302-9

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