Coupling of alkynyl organometallics with 4-acetoxy-1,3-dioxanes: Synthesis of propargylic and allylic anti-1,3-diols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. General Synthesis of α-Acetoxy Ethers from Esters by DIBALH Reduction and Acetylation
2. Stereoselective Radical and Cationic Couplings in 4-Acetoxy-1,3-Dioxane Rings
3. A Critical Evaluation of the Cationic Coupling of 4-Acetoxy-1,3-Dioxanes
4. Dialkylzinc Additions to 4-Acetoxy-1,3-dioxanes: A Highly Stereoselective Route to Protected anti-1,3-Diols
5. Conversion of glycosyl fluorides into -glycosides using organoaluminum reagents. Stereospecific alkylation at C-6 of a pyranose sugar
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1. The Chemistry of Alkynylaluminum Species;PATAI'S Chemistry of Functional Groups;2016-12-15
2. A General Access to Propargylic Ethers through Brønsted Acid Catalyzed Alkynylation of Acetals and Ketals with Trifluoroborates;Chemistry - A European Journal;2015-08-06
3. Synthesis of a vinylchlorine-containing 1,3-diol from a marine cyanophyte;Tetrahedron;2014-07
4. Aluminum, Dimethyl(2-phenylethynyl) [Dimethyl Aluminum Phenyl Acetylide];Encyclopedia of Reagents for Organic Synthesis;2012-03-15
5. Dialkylaluminium‐, ‐Gallium‐, and ‐Indium‐Based Poly‐Lewis Acids with a 1,8‐Diethynylanthracene Backbone;Chemistry – A European Journal;2010-09-09
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