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Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di- and Triborylated Indoles.


ABSTRACT: Bismuth(III) acetate is a safe, inexpensive, and selective facilitator of sequential protodeboronations, which when used in conjunction with Ir-catalyzed borylations allows access to a diversity of borylated indoles. The versatility of combining Ir-catalyzed borylations with Bi(III)-catalyzed protodeboronation is demonstrated by selectively converting 6-fluoroindole into products with Bpin groups at the 4-, 5-, 7-, 2,7-, 4,7-, 3,5-, and 2,4,7-positions and the late-stage functionalization of sumatriptan.

SUBMITTER: Shen F 

PROVIDER: S-EPMC5080616 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature

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Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di- and Triborylated Indoles.

Shen Fangyi F   Tyagarajan Sriram S   Perera Damith D   Krska Shane W SW   Maligres Peter E PE   Smith Milton R MR   Maleczka Robert E RE  

Organic letters 20160321 7


Bismuth(III) acetate is a safe, inexpensive, and selective facilitator of sequential protodeboronations, which when used in conjunction with Ir-catalyzed borylations allows access to a diversity of borylated indoles. The versatility of combining Ir-catalyzed borylations with Bi(III)-catalyzed protodeboronation is demonstrated by selectively converting 6-fluoroindole into products with Bpin groups at the 4-, 5-, 7-, 2,7-, 4,7-, 3,5-, and 2,4,7-positions and the late-stage functionalization of sum  ...[more]

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