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Synthesis and reactivity of palladiu...
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Culkin, Darcy Ann.
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Synthesis and reactivity of palladium complexes of functionalized alkyls. Selection of catalysts for the alpha-arylation of nitriles and amides.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Synthesis and reactivity of palladium complexes of functionalized alkyls. Selection of catalysts for the alpha-arylation of nitriles and amides./
Author:
Culkin, Darcy Ann.
Description:
285 p.
Notes:
Source: Dissertation Abstracts International, Volume: 65-03, Section: B, page: 1316.
Contained By:
Dissertation Abstracts International65-03B.
Subject:
Chemistry, Inorganic. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3125179
ISBN:
049672469X
Synthesis and reactivity of palladium complexes of functionalized alkyls. Selection of catalysts for the alpha-arylation of nitriles and amides.
Culkin, Darcy Ann.
Synthesis and reactivity of palladium complexes of functionalized alkyls. Selection of catalysts for the alpha-arylation of nitriles and amides.
- 285 p.
Source: Dissertation Abstracts International, Volume: 65-03, Section: B, page: 1316.
Thesis (Ph.D.)--Yale University, 2004.
A series of arylpalladium alkyl complexes containing varied functional groups alpha to the metal was prepared to reveal the effect of ligand steric and electronic properties on structure, stability, and reactivity. Arylpalladium complexes of methyl, benzyl, enolate, cyanoalkyl, and trifluoroethyl groups underwent carbon-carbon bond-forming reductive elimination upon heating. Mechanistic studies of the reductive elimination process led to the discovery of a new coupling reaction, the palladium-catalyzed alpha-arylation of nitriles, and to the development of improved methods for the palladium-catalyzed synthesis of alpha-aryl amides.
ISBN: 049672469XSubjects--Topical Terms:
517253
Chemistry, Inorganic.
Synthesis and reactivity of palladium complexes of functionalized alkyls. Selection of catalysts for the alpha-arylation of nitriles and amides.
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Synthesis and reactivity of palladium complexes of functionalized alkyls. Selection of catalysts for the alpha-arylation of nitriles and amides.
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285 p.
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Source: Dissertation Abstracts International, Volume: 65-03, Section: B, page: 1316.
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Thesis (Ph.D.)--Yale University, 2004.
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A series of arylpalladium alkyl complexes containing varied functional groups alpha to the metal was prepared to reveal the effect of ligand steric and electronic properties on structure, stability, and reactivity. Arylpalladium complexes of methyl, benzyl, enolate, cyanoalkyl, and trifluoroethyl groups underwent carbon-carbon bond-forming reductive elimination upon heating. Mechanistic studies of the reductive elimination process led to the discovery of a new coupling reaction, the palladium-catalyzed alpha-arylation of nitriles, and to the development of improved methods for the palladium-catalyzed synthesis of alpha-aryl amides.
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http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3125179
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