The synthesis of 3,4-dihydro-2(IH)-quinolinones has been accomplished through the rearrangement of ~lactam intermediates on the solid-phase. The ~-laetam intermediates were constructed through [2+2] cycloadditions between ketenes and imines on the solid-phase. A library of 4,140 dihydroquinolinones
Enantiospecific synthesis and absolute configuration of β-lactam, intermediates from 2-amino-1-phenyl-1,3-propanediols
✍ Scribed by Tamas E Gunda; Siegfried Vieth; Katalin E Kövér; Ferenc Sztaricskai
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 162 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.