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Merits and drawbacks of known carbon‐carbon linking procedures are outlined. Two novel methods are discussed in some detail: the copper‐catalyzed alkylation of Grignard reagents and reactions with allylpotassium compounds. Both methods provide a very efficient access to saturated, unsaturated, as well as functionally substituted hydrocarbons and moreover permit an astonishing degree of regio‐ and stereoselective control of olefin synthesis.
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Manfred Schlosser (1974) studied this question.
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