The Birch Reduction is an organic reaction which is chiefly functional in synthetic organic chemistry. The reaction was presented in 1944 by the Australian chemist Arthur Birch (1915-1995) working in the Dyson Perrins Laboratory at the University of Oxford, building on previous work by Wooster and Godfrey in 1937. It changes aromatic compounds owing a benzenoid ring to a product, 1,4-cyclohexadienes, in which two hydrogen atoms have been attach on opposite ends of the molecule.
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