COC(=O)c1ccccc1C>C1=CCCC=CCC1.C1=CCCC=CCC1.CC(C)(C)c1ccnc(-c2cc(C(C)(C)C)ccn2)c1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.COC(C)(C)C.C[OH2+].C[OH2+].[Ir].[Ir]>COC(=O)c1cc(B2OC(C)(C)C(C)(C)O2)ccc1C.COC(=O)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1CGeneral procedure D was applied to methyl 2-methylbenzoate15h(30 mg, 0.2 mmol). The reaction mixture was allowed to stand for 16hoursgiving a conversion of >99%(GC-MS) and 16hand 17hin a 73:27 mixture (1H NMR spectrum).
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