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Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di- and Triborylated Indoles
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 prot...
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Published in: | Organic letters 2016-04, Vol.18 (7), p.1554-1557 |
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Main Authors: | , , , , , , |
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container_end_page | 1557 |
container_issue | 7 |
container_start_page | 1554 |
container_title | Organic letters |
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creator | Shen, Fangyi Tyagarajan, Sriram Perera, Damith Krska, Shane W Maligres, Peter E Smith, Milton R Maleczka, Robert E |
description | 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. |
doi_str_mv | 10.1021/acs.orglett.6b00356 |
format | article |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Acetates - chemistry Bismuth - chemistry Boron Compounds - chemistry Catalysis Indoles - chemistry Molecular Structure |
title | Bismuth Acetate as a Catalyst for the Sequential Protodeboronation of Di- and Triborylated Indoles |
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