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Dirhodium(II)-catalyzed carbonyl ylide generation. Stereoelectronic control in dioxolane formation

✍ Scribed by M. P. Doyle; D. C. Forbes; K. R. Xavier

Book ID
105597733
Publisher
Springer
Year
1998
Tongue
English
Weight
356 KB
Volume
47
Category
Article
ISSN
1573-9171

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πŸ“œ SIMILAR VOLUMES

Enantioselective intermolecular 1,3-dipo
Enantioselective intermolecular 1,3-dipolar cycloaddition via ester-derived carbonyl ylide formation catalyzed by chiral dirhodium(II) carboxylates
✍ Shinji Kitagaki; Motoki Yasugahira; Masahiro Anada; Makoto Nakajima; Shunichi Ha πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 198 KB

Enantioselective 1,3-dipolar cycloaddition of the ester-carbonyl ylides derived from methyl 2-(diazoacetyl)benzoate and 3-(diazoacetyl)-2-naphthoate with dipolarophiles has been eected with the aid of dirhodium(II) tetrakis[N-phthaloyl-(S)-tert-leucinate], aording cycloadducts in up to 93% ee.

ChemInform Abstract: Enantioselective In
ChemInform Abstract: Enantioselective Intermolecular 1,3-Dipolar Cycloaddition via Ester-Derived Carbonyl Ylide Formation Catalyzed by Chiral Dirhodium(II) Carboxylates.
✍ Shinji Kitagaki; Motoki Yasugahira; Masahiro Anada; Makoto Nakajima; Shunichi Ha πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons βš– 34 KB πŸ‘ 1 views

## 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 β€œFull Text” option. The original article is trackable v