Formal [4 + 2] Intramolecular Ketenimine-Imine Cycloaddition. Synthesis of Benzimidazo[1,2-b]isoquinolines. -Formal [4+2] cycloaddition of ketenimine intermediates (V) derived from the azides (III) and diphenylketene (IV) by aza-Wittig reaction, provides the partially saturated compounds (VI). They
✦ LIBER ✦
Formal [4+2] intramolecular cycloaddition ketenimine-imine. Synthesis of benzimidazo[1,2-b]isoquinolines
✍ Scribed by Mateo Alajarín; Ángel Vidal; Fulgencio Tovar; Carlota Conesa
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 181 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Benzimidazo [1,2-b]isoquinolines have been prepared by a formal [4+2] intramolecular cycloaddition of ketenimines with imines.
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## Abstract For Abstract see ChemInform Abstract in Full Text.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v