C. J. Kim

Product-rate correlation in acetolysis of threo-3-aryl-2-butyl brosylates. Supporting evidence for the existence of two discrete pathways

Structural Effects in Solvolytic Reactions. II. Nature of the Intermediates Involved in the Solvolysis of Symmetrically Substituted β-Anisylethyl Derivatives

Structural effects in solvolytic reactions. III. Nature of the intermediate involved in the solvolysis of 3-aryl-2,3-dimethyl-2-butyl derivatives

Structural effects in solvolytic reactions. IV. Rates and products in the acetolysis of substituted 3-phenyl-2-butyl brosylates. Nature of the reaction pathway in the acetolysis of secondary alkyl arenesulfonates

Structural effects in solvolytic reactions. VI. Rates and products in the acetolysis of substituted trans-2-phenylcyclopentyl tosylates and optically active derivatives. Nature of the aryl-assisted and the aryl-unassisted reaction pathways

Structural effects in solvolytic reactions. V. Rates and products in the acetolysis of substituted cis-2-phenylcyclopentyl tosylates and deuterium tagged derivatives. Nature of the reaction pathway in the absence of aryl participation

Rates and products of acetolysis of trans-2-arylcyclopentyl tosylates. Evidence for major control of the stereochemistry of the substitution process by neighboring aryl in the absence of rate accelerations

Rates and products of acetolysis of threo-3-aryl-2-butyl brosylates. An experimental approach to the magnitude of rate accelerations attributable to aryl participation in the acetolysis and the stereochemical consequences

Rates and products of acetolysis of cis-2-arylcyclopentyl tosylates and a deuterium-tagged derivative, 1-d1-cis-2-phenylcyclopentyl tosylate

STRUKTUREINFLUESSE AUF SOLVOLYTISCHE RK. 6. MITT. GESCHWINDIGKEITEN UND PRODUKTE BEI DER ACETOLYSE SUBSTITUIERTER TRANS-2-PHENYL-CYCLOPENTYLTOSYLATE