Ring-opening of glycidyl derivatives by silanes mediated by Ti(O-il-Pr)4 or Al(O-i-Pr)3: Access to versatile C3 building blocks.
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference14 articles.
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2. Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization
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5. Glycidyl derivatives as chiral C3 synthons. Ring opening catalyzed by boron trifluoride etherate
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1. Synthesis of (Z)-fluoroallyl azides through aluminium-mediated defluorinative functionalization reactions;Tetrahedron Letters;2015-02
2. Cyanotrimethylsilane;Encyclopedia of Reagents for Organic Synthesis;2011-09-15
3. ChemInform Abstract: Ring Opening of Glycidyl Derivatives by Silanes Mediated by Ti(O-iPr)4 or Al(O-iPr)3: Access to Versatile C3 Building Blocks.;ChemInform;2010-08-22
4. Enantioselective desymmetrization of phospholene meso-epoxide by nucleophilic opening of the epoxide;Tetrahedron: Asymmetry;2004-01
5. Glycidyl Tosylate;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
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