Asymmetric Sulfur Ylide Mediated Aziridination: Application in the Synthesis of the Side Chain of Taxol
- 24 September 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 5 (21), 3987-3990
- https://doi.org/10.1021/ol035554w
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Sulfur‐Ylide‐Mediated Synthesis of Functionalized and Trisubstituted Epoxides with High Enantioselectivity; Application to the Synthesis of CDP‐840Angewandte Chemie-International Edition, 2003
- A Regio- and Stereodivergent Route to All Isomers of vic-Amino AlcoholsThe Journal of Organic Chemistry, 2002
- Chemoenzymatic synthesis of the C-13 side chain of paclitaxel (Taxol) and docetaxel (Taxotere)Tetrahedron: Asymmetry, 2000
- A Regio- and Stereodivergent Synthesis of vic-Amino AlcoholsOrganic Letters, 2000
- A Highly Stereoselective Aza-[3,3]-Claisen Rearrangement of Vinylaziridines as a Novel Entry to Seven-Membered LactamsJournal of the American Chemical Society, 1997
- Catalytic Asymmetric Aminohydroxylation (AA) of OlefinsAngewandte Chemie-International Edition, 1996
- N-[1-(Benzotriazol-1-yl)alkyl]amides, versatile amidoalkylation reagents. 5. A general and convenient route to N-(.alpha.-alkoxyalkyl)amidesThe Journal of Organic Chemistry, 1992
- An efficient, enantioselective synthesis of the taxol side chainThe Journal of Organic Chemistry, 1986
- A Facile Method for the Synthesis of SubstitutedN-Methylenecarboxamides and AlkylN-MethylenecarbamatesSynthesis, 1984
- A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compoundsThe Journal of Organic Chemistry, 1981