A tripartite asymmetric allylboration — Silicon tethered alkene ring closing metathesis — in situ ring opening protocol for the regiospecific generation of functionalized (E)-disubstituted homoallylic alcohols
- 12 March 1999
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 55 (11) , 3219-3232
- https://doi.org/10.1016/s0040-4020(98)01135-1
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Stereoselective Synthesis of 2,3,5-Trisubstituted Tetrahydrofurans by an Allyl Silane Metathesis - Nucleophilic Addition SequenceSynlett, 1997
- Tandem asymmetric allylboration–alkene metathesis: a novel strategy for the synthesis of trans-disubstituted homoallylic alcoholsChemical Communications, 1996
- Regio- and Stereochemical Aspects of the Palladium-Catalyzed Reactions of SilanesChemical Reviews, 1995
- Selective reactions using allylic metalsChemical Reviews, 1993
- Total synthesis of rapamycinJournal of the American Chemical Society, 1993
- A(1,3) strain-Controlled Cyclic Hydroboration of 1,4- and 1,5-DienesChemistry Letters, 1989
- Stereoselective synthesis of alcohols, XXVIII. Stereocontrol of addition of chiral ( E )‐(α‐chlorocrotyl)boronates to chiral aldehydesEuropean Journal of Inorganic Chemistry, 1988
- Stereoselective synthesis of alcohols, XXII. E/Z‐selectivity on addition of α‐substituted allylboronates to aldehydesEuropean Journal of Inorganic Chemistry, 1986
- Enantiomeric Z- and E-crotyldiisopinocampheylboranes. Synthesis in high optical purity of all four possible stereoisomers of .beta.-methylhomoallyl alcoholsJournal of the American Chemical Society, 1986
- Generation, nuclear magnetic resonance spectra, and alkylation of enolates from trialkylsilyl enol ethersJournal of the American Chemical Society, 1968