ChemInform Abstract: New Cyclizing Agents in the Synthesis of β-Ionone from Pseudoionone.
✍ Scribed by Yu. D. Markovich; A. V. Panfilov; Yu. N. Platunov; A. A. Zhirov; S. I. Kosenko; A. T. Kirsanov
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
New Cyclizing Agents in the Synthesis of β-Ionone from Pseudoionone.
-The cyclization of pseudoionone (I) to β-ionone (III) is achieved in excellent selectivity using mixtures of trifluoroacetic acid with sulfuric or fluorosulfonic acid (5.5 : 1-1.25). Additionally, these mixtures can be used directly to transform α-ionone (II) to the β-isomer (III). -(MARKOVICH, YU. D.;
📜 SIMILAR VOLUMES
## 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
## Abstract Darzens condensation under optimized conditions gives novel α,β‐epoxyketones (III) and (V) which are evaluated for their anticancer activity in vitro.
Lipase-Mediated Synthesis of the Enantiomeric Forms of 4,5-Epoxy-4,5-dihydro-α-ionone and 5,6-Epoxy-5,6-dihydro-β-ionone. A New Direct Access to Enantiopure (R)-and (S)-α-Ionone. -In continuation of a recent study a lipase-mediated approach to optically active α-ionone starting from its racemate is
## 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