65499-26-5Relevant academic research and scientific papers
3-Hydroxy-2-oxo-1-oxaspiro[4.5]-dec-3-ene, a new inhibitor of lactate dehydrogenase
Kato, Yasuo
, p. 4809 - 4812 (1995)
Methods for the synthesis of the spirolactone [3-hydroxy-2-oxo-1-oxaspiro[4.5]-dec-3-ene, 3] and the sodium salts of two new α-keto acids [(1-cyclohexenyl)glyoxylate 1, β-(1-hydroxycyclohexane)pyruvate (enol form, 2)] are described. These compounds are ex
Synthesis and biological activity of new C-6 and C-7 substituted vinyloxyimino-penicillins and -cephalosporins
Fell, Stephen C. M.,Pearson, Michael J.,Burton, George,Elder, John S.
, p. 1483 - 1494 (2007/10/02)
The Wittig reaction has been successfully utilized in the preparation of a number of substituted α-vinyloxyiminoacetic acids, the subsequent coupling of which to the 6-APA and 7-ACA nuclei has provided a range of potent β-lactam antibiotics.Development of other procedures for olefin synthesis has broadened the scope, with the preparation of a range of alkenyl-, cycloalkenyl- and arylvinyl-oxyiminoacetamidopenicillins and cephalosporins.
INTRAMOLECULAR NITRONE-ALKYNE CYCLOADDITION
Kang, Han-Young,Cho, Yong Seo,Koh, Hun Yeong,Chang, Moon Ho
, p. 2779 - 2782 (2007/10/02)
It is demonstrated that the cycloaddition of a nitrone to an alkyne is facile when the length of the tether connecting the two reacting sites is appropriate.The resulting cycloaddition products, isoxazolidines can be further converted to 3-hyd
