## Abstract Trisubstituted 1,4,5,6,โtetrahydroโ7__H__โindolones are obtained in a oneโpot synthesis from conjugated nitroolefins and ฮฑโketoenamines derived from ฮฑโamino esters and cyclohexaneโ1,2โdione. In some cases bicyclo[3.2.1]octanโ8โone and 1,2โoxazine __N__โoxide derivatives are isolated.
โฆ LIBER โฆ
Synthesis of optically active (pivaloyloxy)methyl 2',3'-substituted 4'-oxoazetidin-1'-yl-3-methylbut-2-enoates from 6-apa
โ 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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โฆ 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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