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Synthesis of optically active (pivaloyloxy)methyl 2',3'-substituted 4'-oxoazetidin-1'-yl-3-methylbut-2-enoates from 6-apa

โœ Scribed by Carmen Somoza; Oreste A. Mascaretti


Book ID
104203685
Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
599 KB
Volume
44
Category
Article
ISSN
0040-4020

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โœฆ Synopsis


The title compound were prepared aa useful optically active intermediates for the syntheals of "non-classical" B-lactam compounds. These monocyclic atetidinones were formed by cleavage of sulfur-carbon 5 bond of bicyclic penlcillanates with chlorine or tert-butyl hypochlorite in approplate solvents.


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Synthesis of optically active 1,2,3-subs
โœ P. Nitti; G. Pitacco; A. Pizzioli; E. Valentin ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Journal of Heterocyclic Chemistry ๐ŸŒ English โš– 559 KB

## Abstract Trisubstituted 1,4,5,6,โ€tetrahydroโ€7__H__โ€indolones are obtained in a oneโ€pot synthesis from conjugated nitroolefins and ฮฑโ€ketoenamines derived from ฮฑโ€amino esters and cyclohexaneโ€1,2โ€dione. In some cases bicyclo[3.2.1]octanโ€8โ€one and 1,2โ€oxazine __N__โ€oxide derivatives are isolated.