Unsymmetrical alkenes by carbene coupling from diazirine decomposition in the presence of diazo compounds
…, KE Bassett, JW Terpstra, SN Mahapatro
Index: Doyle, Michael P.; Devia, Alvaro H.; Bassett, Kathlene E.; Terpstra, Jan W.; Mahapatro, Surendra N. Journal of Organic Chemistry, 1987 , vol. 52, # 8 p. 1619 - 1621
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Citation Number: 16
Abstract
resulted in nearly quantitative azine formation, decomposition of an equimolar mixture of these two diazirines produced the carbene dimer from this reactant combination without azine. The mixed carbene dimer was proposed to have resulted from nucleophilic attack of 1- phenyldiazoethane, presumed to have been formed from 3-methyl-3-phenyl-diazirine, on chlorophenylcarbene (eq
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