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Org Lett ; 18(7): 1554-7, 2016 Apr 01.
Article in English | MEDLINE | ID: mdl-26998615

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.


Subject(s)
Acetates/chemistry , Bismuth/chemistry , Boron Compounds/chemistry , Indoles/chemistry , Catalysis , Molecular Structure
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