(PDF) REACTION OF PROPARGYL BROMIDE AND

REACTION OF PROPARGYL BROMIDE AND TRIMETHYLSILYLPROPARGYL IODIDE WITH METALLIC TIN, ALUMINUM, AND ALDEHYDES OR KETONES. SELECTIVE SYNTHESIS OF Β-Acetylene, Β-Trimethylsilylacetylene, AND Α-Trimethylsilylallene ALCOHOLS

Chemistry Letters - Japan

doi 10.1246/cl.1984.1939

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November 5, 1984

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The Chemical Society of Japan

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REACTION OF PROPARGYL BROMIDE AND TRIMETHYLSILYLPROPARGYL IODIDE WITH METALLIC TIN, ALUMINUM, AND ALDEHYDES OR KETONES. SELECTIVE SYNTHESIS OF Β-Acetylene, Β-Trimethylsilylacetylene, AND Α-Trimethylsilylallene ALCOHOLS

Chemistry Letters - Japan

doi 10.1246/cl.1984.1939

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Regioselective Synthesis of Β-Fluoro-Α,β-Unsaturated Ketones by the Reaction of Β-Diketones With DFMBA

One-Pot Synthesis of Α,β-Unsaturated Esters, Ketones, and Nitriles From Alcohols and Phosphonium Salts

Direct Asymmetric Michael Reaction of Α,β-Unsaturated Aldehydes and Ketones Catalyzed by Two Secondary Amine Catalysts

Reaction Mode of N-Butylmagnesium Bromide and Α, Β-Unsaturated Carbonyl Compounds

Stereoretentive Addition ofN-tert-Butylsulfonyl-α-Amido Silanes to Aldehydes, Ketones, Α,β-Unsaturated Esters, and Imines

Cover Picture: Highly Selective Reduction of Α, Β -Unsaturated Aldehydes and Ketones Under Ambient Conditions Using Tetraalkylphosphonium-Based Ionic Liquids (42/2018)

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Selective Synthesis of Β-Amino Esters and Β-Lactams by Rhodium-Catalyzed Reformatsky-Type Reaction

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