[3+2] cycloadditions of allylsilanes - 4.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
1. Chemistry of organosilicon compounds. 99. Conjugate addition of allylsilanes to .alpha.,.beta.-enones. A New method of stereoselective introduction of the angular allyl group in fused cyclic .alpha.,.beta.-enones
2. Stereochemistry of the Sakurai reaction. Additions to cyclohexenones and cycloheptenones
3. Conjugate Addition of Allylsilanes with Subsequent Sila-Wagner-Meerwein Rearrangement: A Novel Methodology for Stereoselective Trimethylsilylcyclopentane Annulation
4. Transition Metal-Diene Complexes in Organic Synthesis; Part 6.1Stereoselective Synthesis of Iron-Complexed 4b,8a-Dihydrocarbazol-3-ones: A Novel Route to 4a,9a-Dihydro-9H-carbazoles and Highly Chemo-, Regio-, and Stereoselective Sakurai Reactions
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1. Synthesis of Enantiopure Triols from Racemic Baylis–Hillman Adducts Using a Diastereoselective Peroxidation Reaction;Organic Letters;2020-11-03
2. Indium-Catalyzed [2 + 2] Cycloaddition of Allylsilanes to Internal Alkynones;Organic Letters;2015-11-19
3. Synthesis and functionalization of bicyclic N,O-acetal scaffolds from furfural;Bioorganic & Medicinal Chemistry;2015-06
4. Stereoselective Construction of 1,3-Disilylcyclopentane Derivatives by Scandium-Catalyzed [3+2] Cycloaddition of Allylsilanes to β-Silylenones;Angewandte Chemie International Edition;2014-07-27
5. Stereoselective Construction of 1,3-Disilylcyclopentane Derivatives by Scandium-Catalyzed [3+2] Cycloaddition of Allylsilanes to β-Silylenones;Angewandte Chemie;2014-07-25
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