Acceptor-substituted cycloalkenones 1 undergo an iron(III)catalyzed vinylogous Michael reactiona sequence of enone-dienol tautomerism, [4+2]-cycloaddition, and retro-aldol reactionwith quinone derivatives 3. A variety of products is obtained ranging from meta-terphenyl precursors 5 to
Vinylogous Pyridinecarbaldehydes by Wittig Reaction
β Scribed by Prof. Dr. Ilse Hagedorn; Dr. Wolfram Hohler
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 122 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
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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 βFull Textβ option. The original article is trackable v
## 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 βFull Textβ option. The original article is trackable v