The palladium(0)-catalyzed reaction of derivatives of g-amino-a,b-unsaturated esters bearing an N-(2-iodobenzoyl) substituent results in an intramolecular Heck reaction, the outcome of which depends on the structure of the substrate as well as on the experimental conditions. The methodology develope
ChemInform Abstract: Efficient Synthesis of Chiral Isoquinoline and Pyrido[1,2-b]isoquinoline Derivatives via Intramolecular Heck Reactions.
β Scribed by Francisco Sanchez-Sancho; Enrique Mann; Bernardo Herradon
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Abstract
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π SIMILAR VOLUMES
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
## 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 of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v