Differentially protected benzenediboronic acids: divalent cross-coupling modules for the efficient synthesis of boron-substituted oligoarenes
H Noguchi, T Shioda, CM Chou, M Suginome
Index: Noguchi, Hiroyoshi; Shioda, Takayuki; Chou, Chih-Ming; Suginome, Michinori Organic Letters, 2008 , vol. 10, # 3 p. 377 - 380
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Citation Number: 112
Abstract
On the basis of the boron-masking strategy, new divalent cross-coupling modules have been designed for the efficient synthesis of boron-substituted oligoarenes. The modules, ie, monoprotected o-, m-, and p-benzenediboronic acid derivatives, undergo highly selective Suzuki-Miyaura coupling with sp2 iodides, bromides, chlorides, and triflates, affording coupling products in which the protected boronyl groups are left intact.
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