4.8 Article

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

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ORGANIC LETTERS
卷 18, 期 7, 页码 1554-1557

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b00356

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资金

  1. NIH [GM63188]
  2. NSF [GOALI-1012883]
  3. Merck
  4. ACS/GCI Pharmaceutical Roundtable
  5. Thomas J. Pinnavaia Fellowship

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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.

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