## Abstract For Abstract see ChemInform Abstract in Full Text.
Enantioselectively catalyzed intramolecular cyclopropanations of unsaturated diazo carbonyl compounds
✍ Scribed by William G. Dauben; Robert T. Hendricks; Michael J. Luzzio; Howard P. Ng
- Book ID
- 104228511
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 366 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A series of unsaturated a-diazo carbonyl compounds umierwent enantioselective intramolecular cyclopropanation (ee = 4-77%) when treated with an enantiomerically pure chiral copper catalyst. The nature of the diazo substrate was critical: a-diazo ketones gave the best &antioselectivities whereas a-diazo p-keto ester systems showed diminished enantioselectivities.
📜 SIMILAR VOLUMES
## Abstract The intermolecular cyclopropanation of styrene with ethyl diazo(triethylsilyl)acetate (**1a**) proceeds at room temperature in the presence of chiral Rh^II^ carboxylate catalysts derived from imide‐protected amino acids and affords mixtures of __trans__‐ and __cis__‐cyclopropane derivat
Dedicated to Professor Paul Müller on the occasion of his 65th birthday and retirement from the University of Geneva Different classes of cyclopropanes derived from Meldrums acid ( 2,2-dimethyl-1,3-dioxane-4,6-dione; 4), dimethyl malonate (5), 2-diazo-3-(silyloxy)but-3-enoate 16, 2-diazo-3,3,3-trifl