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Mechanism of substitution at a saturated carbon atom - Part XXIII - A kinetic demonstration of the unimolecular solvolysis of alkyl halides - (Section E) A general discussion
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JOURNAL OF THE CHEMICAL SOCIETY,
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DIRECTIVE EFFECTS IN AROMATIC SUBSTITUTION .26. RATES OF SOLVOLYSIS OF THE META-PHENYL AND PARA-PHENYL, META-METHYLTHIO AND PARA-METHYLTHIO AND META-TRIMETHYLSILYLPHENYLDIMETHYLCARBINYL AND PARA TRIMETHYLSILYLPHENYLDIMETHYLCARBINYL CHLORIDES - STERIC INHIBITION OF RESONANCE AS A FACTOR IN ELECTROPHILIC SUBSTITUENT CONSTANTS
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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
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BROWN HC, 1958, STERIC EFFECTS CONJU, P100
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THE KINETICS AND MECHANISMS OF NUCLEOPHILIC DISPLACEMENTS IN ALLYLIC SYSTEMS .6. SOLVOLYSIS AND THE ACCOMPANYING REARRANGEMENT OF 1-1-DIMETHYLALLYL AND OF 3-3-DIMETHYLALLYL CHLORIDE
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JOURNAL OF THE CHEMICAL SOCIETY,
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