Issue 0, 1985

Studies on lactams. Part 74. An approach to the total synthesis of amino sugars viaβ-lactams

Abstract

Convenient intermediates for mono- and di-amino sugars related to antibiotics can be prepared in a stereocontrolled fashion by the rearrangement of 3,4-disubstituted azetidin-2-ones which in turn can be synthesized by stereoselective annelation of certain imino compounds by substituted acetic acid derivatives.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1985, 2045-2050

Studies on lactams. Part 74. An approach to the total synthesis of amino sugars viaβ-lactams

M. S. Manhas, V. R. Hegde, D. R. Wagle and A. K. Bose, J. Chem. Soc., Perkin Trans. 1, 1985, 2045 DOI: 10.1039/P19850002045

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