Reduktive Ringöffnung von Oxabicyclen mit Diisobutylaluminiumhydrid ‐ Anwendung bei der Synthese der C17‐C23‐Untereinheit von Ionomycin
- 1 February 1993
- journal article
- Published by Wiley in Angewandte Chemie
- Vol. 105 (2) , 267-269
- https://doi.org/10.1002/ange.19931050217
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- A formal total synthesis of (+)-macbecin IThe Journal of Organic Chemistry, 1992
- Asymmetric synthesis of macbecin IThe Journal of Organic Chemistry, 1992
- Stabilized Nucleophiles with Electron Deficient Alkenes and AlkynesPublished by Elsevier ,1991
- The Aldol Reaction: Acid and General Base CatalysisPublished by Elsevier ,1991
- Opening of oxabicyclo[3.2.1]octenes with organolithium reagents. A route to cyclic and acyclic compounds with high stereocontrolThe Journal of Organic Chemistry, 1990
- The total synthesis of (+)-ionomycinJournal of the American Chemical Society, 1990
- Chiral synthesis via organoboranes. 6. Hydroboration. 74. Asymmetric hydroboration of representative heterocyclic olefins with diisopinocampheylborane. Synthesis of heterocyclic boronates and heterocyclic alcohols of very high enantiomeric purityJournal of the American Chemical Society, 1986
- Stereoselective method for the synthesis of both olefinic isomers from a single precursor. Conjugate reduction of .alpha.,.beta.-unsaturated epoxidesJournal of the American Chemical Society, 1973
- Hydroboration of dihydropyrans and dihydrofuransThe Journal of Organic Chemistry, 1970
- Metallorganische Verbindungen XIX: Reaktionen der Aluminium‐ Wasserstoff‐Bindung mit OlefinenEuropean Journal of Organic Chemistry, 1954