ChemInform Abstract: Novel and Efficient Entry to γ-Aryl-Substituted γ,δ-Unsaturated Ketones,...

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1999 polyphenylalkane derivatives polyphenylalkane derivatives Q 0720 24 - 098 Novel and Efficient Entry to γ-Aryl-Substituted γ,δ-Unsaturated Ketones, Amides, Nitriles, and Sulfones by Conjugate Additions of 2-Benzotriazolylethylsilanes. — A variety of γ,δ-unsaturated title compounds is readily prepared from 2-benzotriazolyl-2-arylethylsilanes (I). The simple method allows a variety of substituents. — (KATRITZKY, ALAN R.; VORONKOV, MICHAEL V.; TOADER, DORIN; J. Org. Chem. 63 (1998) 26, 9987-9988; Cent. Heterocycl. Comp., Dep. Chem., Univ. Fla., Gainesville, FL 32611, USA; EN) 1

Transcript of ChemInform Abstract: Novel and Efficient Entry to γ-Aryl-Substituted γ,δ-Unsaturated Ketones,...

Page 1: ChemInform Abstract: Novel and Efficient Entry to γ-Aryl-Substituted γ,δ-Unsaturated Ketones, Amides, Nitriles, and Sulfones by Conjugate Additions of 2-Benzotriazolylethylsilanes.

1999 polyphenylalkane derivatives

polyphenylalkane derivativesQ 0720

24 - 098Novel and Efficient Entry to γ-Aryl-Substituted γ,δ-UnsaturatedKetones, Amides, Nitriles, and Sulfones by Conjugate Additionsof 2-Benzotriazolylethylsilanes. — A variety of γ,δ-unsaturated titlecompounds is readily prepared from 2-benzotriazolyl-2-arylethylsilanes (I). Thesimple method allows a variety of substituents. — (KATRITZKY, ALAN R.;VORONKOV, MICHAEL V.; TOADER, DORIN; J. Org. Chem. 63 (1998) 26,9987-9988; Cent. Heterocycl. Comp., Dep. Chem., Univ. Fla., Gainesville, FL32611, USA; EN)

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Stereoselective Nucleophilic Additions to Aldehydes and ...528536/FULLTEXT01.pdfThis thesis deals with the development of new reaction methodology as well as stereochemical investigations.

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Visible‐Light‐Mediated Decarboxylative Radical Additions to Vinyl … · Visible-Light-Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to g-Amino

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substituent. reactions of α-diazo-β-keto sulfones, α-diazo-β-keto … · 2017. 2. 28. · S1 Enantioselective copper catalysed intramolecular C–H insertion reactions of α-diazo-β-keto

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