反応式
CSc1ccc(Cl)cc1>C1=CCCC=CCC1.C1=CCCC=CCC1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.C[OH2+].C[OH2+].Cc1ccc(C)cc1.FC(F)(F)C1COB(c2ccccc2-c2ccc(-c3ccccn3)nc2)O1.[Ir].[Ir]>CSc1ccc(Cl)c(B2OC(C)(C)C(C)(C)O2)c1.CSc1ccc(Cl)cc1B1OC(C)(C)C(C)(C)O1参加物
7
反応物 1
生成物 2
試薬・触媒・溶媒 4
反応条件
- 温度
- 55 °C
実験手順
Ligand 3f: A mixture of ortho- and meta-borylated products (114 mg, 80% yield, ortho/meta + para = 12); ortho-borylated product 4e was obtained by further purification by GPC (70 mg, 49% yield), white solid (mp. 80-82 oC);
出典と根拠
- ORDレコード
- ord-903f8118d14f42ecaa64e874e6518ce2
- 出典データセット
- Borylation dataset from Roche
関連ノート
読み込み中…