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ChemInform Abstract: The 2,4,6‐Tris(trifluoromethyl)phenyl Substituent. Examples for Electronic and Steric‐Stabilized Low‐Coordinated Elements of the Main Groups.

Mario Scholz, H.W. Roesky, D. Stalke, K. KELLER, Frank T. Edelmann

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Abstract

Abstract Tris(trifluoromethyl)benzene (I) reacts with PCl3 (II) after lithiation to give the phosphonous dichloride (III) which is reduced, yielding the phosphine (IV).

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What this paper is about

Abstract Tris(trifluoromethyl)benzene (I) reacts with PCl3 (II) after lithiation to give the phosphonous dichloride (III) which is reduced, yielding the phosphine (IV).

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Available abstract

Abstract Tris(trifluoromethyl)benzene (I) reacts with PCl3 (II) after lithiation to give the phosphonous dichloride (III) which is reduced, yielding the phosphine (IV).

Key concepts: Chemistry, Trifluoromethyl, Substituent, Steric effects, Tris, Benzene, Phosphine, Medicinal chemistry

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ChemInform Abstract: The 2,4,6‐Tris(trifluoromethyl)phenyl Substituent. Examples for Electronic and Steric‐Stabilized Low‐Coordinated Elements of the Main Groups. — Research Paper | ScholarLens