Effect of catalyst on the diastereoselectivity of methyl phenyldiazoacetate cyclopropanations
- 26 November 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (48) , 8811-8812
- https://doi.org/10.1016/s0040-4039(98)01985-6
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Novel chiral dirhodium catalysts derived from aziridine and azetidine carboxylic acid for intermolecular cyclopropanation reactions with methyl phenyldiazoacetateTetrahedron, 1998
- Chiral catalysts for enantioselective intermolecular cyclopropanation reactions with methyl phenyldiazoacetate. Origin of the solvent effect in reactions catalyzed by homochiral dirhodium(II) prolinatesTetrahedron Letters, 1996
- Effect of diazoalkane structure on the stereoselectivity of rhodium(II) (S)-N-(arylsulfonyl)prolinate catalyzed cyclopropanationsTetrahedron Letters, 1996
- Asymmetric Cyclopropanations by Rhodium(II) N-(Arylsulfonyl)prolinate Catalyzed Decomposition of Vinyldiazomethanes in the Presence of Alkenes. Practical Enantioselective Synthesis of the Four Stereoisomers of 2-Phenylcyclopropan-1-amino AcidJournal of the American Chemical Society, 1996
- Enantioselective synthesis of vinylcyclopropanes by rhodium(II) catalyzed decomposition of vinyldiazomethanes in the presence of alkenesTetrahedron Letters, 1993