Ruthenium-Catalyzed Addition of Carbon-Hydrogen Bonds in Aromatic Ketones to Olefins. The Effect of Various Substituents at the Aromatic Ring. -The investigations reveal that the ortho C-H bond in acetophenone derivatives can be cleaved and added to (II) in the presence of a Ru-catalyst. Both elect
Directing effect of functional groups in ruthenium-catalyzed addition of substituted acetophonones to an olefin
β Scribed by Motohiro Sonoda; Fumitoshi Kakiuchi; Naoto Chatani; Shinji Murai
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 152 KB
- Volume
- 504
- Category
- Article
- ISSN
- 0022-328X
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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
We show here the first example of a ruthenium catalyzed ene-yne metathesis reaction in tandem with a Diels-Alder cycloaddition reaction to efficiently form highly substituted hexahydroisoindole ring systems on Wang resin. This approach was used to prepare a 4200 membered combinatorial library.