Teritary Amine-Accelerated Allylgallation of Terminal Alkynes
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概要
- 論文の詳細を見る
- 2002-02-05
著者
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Takai Kazuhiko
Department Of Applied Chemistry Faculty Of Engineering Okayama University
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IKAWA Yoshito
Department of Applied Chemistry, Faculty of Engineering, Okayama University
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ISHII Keijiro
Department of Applied Chemistry, Faculty of Engineering, Okayama University
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KUMANDA Makoto
Department of Applied Chemistry, Faculty of Engineering, Okayama University
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Ishii K
Department Of Applied Chemistry Faculty Of Engineering Okayama University
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Ikawa Yoshito
Department Of Applied Chemistry Faculty Of Engineering Okayama University
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Kumanda Makoto
Department Of Applied Chemistry Faculty Of Engineering Okayama University
関連論文
- Improved Synthesis and Crystal Structure of TiCl_3 (tmeda) (thf): A Highly Stereoselective Pinacol Coupling Reagent for Aromatic Aldehydes
- Selective Cyclotrimerization of Acetylenes via Tantalum-Alkyne Complexes
- Alkylidenation of Ketones by gem-Dibromoalkane, SmI_2, and Sm in the Presence of Catalytic Amount of CrCl_3
- Reaction of Tantalum-Alkyne Complexes with Hydrazones. Stereoselective Synthesis of (E)-Allylic Hydrazines.
- Catalytic Performance of Tantalum-η^2-Alkyne Complexes [TaCl_3(R^1C≡CR^2)L_2] for Alkyne Cyclotrimerization
- Successive Carbon-Carbon Bond Formation by Sequential Generation of Radical and Anionic Species with Manganese and Catalytic Amounts of PbCl_2 and Me_3 SiCl
- Nucleophilic addition of organochromium reagents to carbonyl compounds
- Transformation of Aldehydes into (E)-1-Alkenylsilanes and (E)-1-Alkenylboronic Esters with a Catalytic Amount of a Chromium Salt
- 304.TRAINING EFFECT OF MUSCULAR ENDURANCE VIEWED FROM BLOOD FLOW
- DOUBLE ELECTRON CAPTURE PROCESSES IN COLLISIONS OF He^ WITH H_2, N_2, O_2 AND CO AT 1 keV/amu
- CHARGE CHANGING CROSS SECTION MEASUREMENTS IN SLOW COLLISIONS OF Kr^ (q=7-9) WITH Ne, N_2, O_2, and CO
- Teritary Amine-Accelerated Allylgallation of Terminal Alkynes
- Activation of Manganese Metal with a Catalytic Amount of Lead and Me_3SiCl and Its Application to Organic Synthesis
- Cross-coupling reaction between enol phosphates and organoaluminium compounds in the presence of palladium(0) catalyst.
- Isomerization of allylic alcohols catalyzed by vanadium or molybdenum complexes.
- Stereoselective epoxidation of allylic alcohols and dehydrogenative oxidation of secondary alcohols by means of t-butyl hydroperoxide and aluminium reagents.
- Baeyer-Villiger oxidation with Me3SiOOSiMe3 under assistance of SnCl4 or BF3OEt2.
- Chromium(VI) or ruthenium(II) complex catalysis in oxidation of alcohols to aldehydes and ketones by means of bis(trimethylsilyl) peroxide.
- Aliphatic Claisen rearrangement promoted by organoaluminium reagents.