Asymmetric Induction in the Wittig‐Still Rearrangement of Ethers Containing an Allylic Stereocenter – Diastereocontrol by Allylic Oxygen
- 1 January 1990
- journal article
- research article
- Published by Wiley in European Journal of Inorganic Chemistry
- Vol. 123 (1), 153-168
- https://doi.org/10.1002/cber.19901230128
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Regio- and stereo-selectivities in some nucleophilic reactionsPublished by Springer Nature ,2006
- Asymmetric Induction and Simple Diastereoselectivity in the [2,3] Wittig Rearrangement of Ester EnolatesEuropean Journal of Inorganic Chemistry, 1989
- Asymmetric Induction in the [2,3] Wittig Rearrangement The Stereoselective Synthesis of Unsaturated Alcohols with Three Contiguous Stereogenic CentersEuropean Journal of Inorganic Chemistry, 1989
- Stereoselective total synthesis of β-2,7,11-Cembratriene-4,6-diol (β-CBT), a tumor inhibitory constituent of tobacco smokeTetrahedron Letters, 1988
- The [2,3] Wittig rearrangement of tertiary allylic ethers. Application to the synthesis of the C12C25 subunit of zincophorinTetrahedron Letters, 1988
- Stereocontrolled synthesis of A C14-C20 building block for amphotericin B using a novel [2,3] wittig rearrangementTetrahedron Letters, 1988
- Asymmetric Induction in the [2,3] Wittig Rearrangement by Chiral Substituents in the Allyl MoietyAngewandte Chemie International Edition in English, 1988
- Asymmetrische Induktion bei der [2,3]-Wittig-Umlagerung durch chirale Substituenten im AllylteilAngewandte Chemie, 1988
- [2,3]-Wittig sigmatropic rearrangements in organic synthesisChemical Reviews, 1986
- Theory and Modeling of Stereoselective Organic ReactionsScience, 1986