Studies on lactams. Part 74. An approach to the total synthesis of amino sugars viaβ-lactams
- 1 January 1985
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 10,p. 2045-2050
- https://doi.org/10.1039/p19850002045
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.This publication has 4 references indexed in Scilit:
- Total synthesis of optically active N-benzoyldaunosamine from an azetidinoneThe Journal of Organic Chemistry, 1984
- Oxidative N-dearylation of 2-azetidinones. p-Anisidine as a source of azetidinone nitrogenThe Journal of Organic Chemistry, 1982
- Synthesen biologisch wichtiger Kohlenhydrate, 8. Synthese der Evermicose (2,6‐Didesoxy‐3‐ C ‐methyl‐ D ‐ arabino ‐hexose)European Journal of Inorganic Chemistry, 1977
- Aspects of the Chemistry of the Amino SugarsPublished by Elsevier ,1959