Highly anti-selective dihydroxylation of 1,2-dialkyl substituted (Z)-allylic amines: stereoselective synthesis of a d-ribo-phytosphingosine derivative
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference43 articles.
1. anti Selective dihydroxylation by the ketimine derivatives of the allylic amine in monosubstituted olefins
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3. Stereoselective dihydroxylation reactions of γ-amino-α,β-unsaturated esters via their aryl ketimine derivatives
4. Acyclic Stereocontrol Induced by Allylic Alkoxy Groups. Synthetic Applications of Stereoselective Dihydroxylation in Natural Product Synthesis
5. Synthesis of α-hydroxy statine through a facially selective osmylation of a chiral α-amido crotonate
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2. Stereoselective Synthesis of (2S,3R)-3-Hydroxyhomoserine Lactone via anti Selective Dihydroxylation of an OBO Group-Protected Vinyl Glycine Analog;APPL CHEM ENG;2020
3. Recent Progress in Chemical Syntheses of Sphingosines and Phytosphingosines;Synthesis;2016-10-10
4. Enantioselective synthesis of guggultetrol and d-ribo-phytosphingosine tetraacetate via l-proline catalyzed sequential α-aminooxylation/Horner–Wardsworth–Emmons olefination–Sharpless asymmetric dihydroxylation strategy;Tetrahedron: Asymmetry;2015-05
5. (S)-Garner aldehyde derived Baylis-Hillman adduct: A potential substrate for the synthesis of D-lyxo phytosphinosine analogue;Journal of Chemical Sciences;2014-11
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