Reagent controlled addition of chiral sulfur ylides to chiral aldehydes
Author:
Publisher
Beilstein Institut
Subject
Organic Chemistry
Link
https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-1-4.pdf
Reference7 articles.
1. Catalytic, Asymmetric Sulfur Ylide-Mediated Epoxidation of Carbonyl Compounds: Scope, Selectivity, and Applications in Synthesis
2. The complexity of catalysis: origins of enantio- and diastereocontrol in sulfur ylide mediated epoxidation reactions
3. Sulfonium ylide epoxidation reactions: methylene transfer
4. Pyridyl and Furyl Epoxides of More Than 99% Enantiomeric Purities: The Use of a Phosphazene Base
5. P(MeNCH2CH2CH2)3N: An efficient promoter for the generation of nonstable and somewhat stable sulfur ylides from sulfonium salts
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1. A theoretical study on the proton affinity of sulfur ylides;New Journal of Chemistry;2022
2. Highly diastereoselective spiro-cyclopropanation of 2-arylidene-1,3-indanediones and dimethylsulfonium ylides;New Journal of Chemistry;2021
3. Practical and Highly Selective Sulfur Ylide-Mediated Asymmetric Epoxidations and Aziridinations Using a Cheap and Readily Available Chiral Sulfide: Extensive Studies To Map Out Scope, Limitations, and Rationalization of Diastereo- and Enantioselectivities;Journal of the American Chemical Society;2013-07-31
4. A Highly Stereoselective Synthesis of Glycidic Amides Based on a New Class of Chiral Sulfonium Salts: Applications in Asymmetric Synthesis;Chemistry - A European Journal;2012-10-18
5. Bicyclo[2.2.1]heptan-2-one, 7,7-Dimethyl-1-(1S,3S,4R)-2-thiabicyclo[2.2.1]hept-3-yl-, (1S,4R);Encyclopedia of Reagents for Organic Synthesis;2012-09-14
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