Synthetic studies on virantmycin. 2. Total synthesis of unnatural (+)-virantmycin and determination of its absolute stereochemistry
- 1 August 1996
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 52 (32) , 10631-10652
- https://doi.org/10.1016/0040-4020(96)00608-4
Abstract
No abstract availableThis publication has 30 references indexed in Scilit:
- Stereochemistry of (–)-virantmycinJournal of the Chemical Society, Perkin Transactions 1, 1990
- Activation of 7-endo over 6-exo epoxide openings. Synthesis of oxepane and tetrahydropyran systemsJournal of the American Chemical Society, 1989
- Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systemsJournal of the American Chemical Society, 1989
- Assignment of Absolute Configuration for Virantmycin and Synthesis of Its AntipodeChemistry Letters, 1988
- Asymmetric Epoxidation of Allylic Alcohols: The Sharpless EpoxidationSynthesis, 1986
- Stereoselective epoxidations of acyclic allylic alcohols by transition metal-hydroperoxide reagents. Synthesis of dl-C18 Cecropia juvenile hormone from farnesolJournal of the American Chemical Society, 1974
- The absolute configuration of cervicarcin; application of the aromatic chrality methodJournal of the Chemical Society D: Chemical Communications, 1970
- Cleavage of sulfonamides with sodium naphthaleneJournal of the American Chemical Society, 1967
- Reaktionen mit Phosphinalkylenen, VIII. Neue Synthese von Carbonsäuren aus PhosphinalkylenenEuropean Journal of Organic Chemistry, 1964
- Veilchenriechstoffe IX. Über die Synthese der kernmethylierten Jononhomologen 1,1,3,6‐Tetramethyl‐2‐(buten‐21‐ylon‐23)‐cyclohexen‐(2 bzw. 3)Helvetica Chimica Acta, 1940