The intramolecular Pauson-Khand reaction of aza-Baylis-Hillman adducts, which were prepared through the thio-Michael/imino-aldol domino reaction of optically active sulfinimines, was examined and gave optically active cis-and trans-pyrrolidine-fused cyclopentenones in a stereoselective manner.
ChemInform Abstract: Intramolecular Pauson—Khand Reaction of Optically Active Aza-Baylis—Hillman Adducts.
✍ Scribed by Shingo Ishikawa; Fumiaki Noguchi; Hidemitsu Uno; Akio Kamimura
- Book ID
- 102047316
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
The reaction of alkyl‐substituted adducts (I) provides predominantly pyrrolidine‐fused cyclopentanones with cis‐configuration.
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## 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 “Full Text” option. The original article is trackable v