Copper(II)-Catalyzed β-Borylation of Acetylenic Esters in Water
Abstract A method for the β-borylation of alkynoates has been developed. In the presence of bis(pinacolato)diboron and catalytic amounts of both copper(II) and 4-picoline, substituted alkynoates undergo borylation in a regio-, stereo-, and chemoselective fashion. The reaction is performed under mild...
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Veröffentlicht in: | Synthesis (Stuttgart) 2015-08, Vol.47 (15), p.2242-2248 |
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container_title | Synthesis (Stuttgart) |
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creator | Peck, Cheryl L. Calderone, Joseph A. Santos, Webster L. |
description | Abstract
A method for the β-borylation of alkynoates has been developed. In the presence of bis(pinacolato)diboron and catalytic amounts of both copper(II) and 4-picoline, substituted alkynoates undergo borylation in a regio-, stereo-, and chemoselective fashion. The reaction is performed under mild conditions using water as solvent and open to the atmosphere to exclusively afford (
Z
)-β-boryl-α,β-unsaturated esters. |
doi_str_mv | 10.1055/s-0034-1380524 |
format | Article |
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A method for the β-borylation of alkynoates has been developed. In the presence of bis(pinacolato)diboron and catalytic amounts of both copper(II) and 4-picoline, substituted alkynoates undergo borylation in a regio-, stereo-, and chemoselective fashion. The reaction is performed under mild conditions using water as solvent and open to the atmosphere to exclusively afford (
Z
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A method for the β-borylation of alkynoates has been developed. In the presence of bis(pinacolato)diboron and catalytic amounts of both copper(II) and 4-picoline, substituted alkynoates undergo borylation in a regio-, stereo-, and chemoselective fashion. The reaction is performed under mild conditions using water as solvent and open to the atmosphere to exclusively afford (
Z
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A method for the β-borylation of alkynoates has been developed. In the presence of bis(pinacolato)diboron and catalytic amounts of both copper(II) and 4-picoline, substituted alkynoates undergo borylation in a regio-, stereo-, and chemoselective fashion. The reaction is performed under mild conditions using water as solvent and open to the atmosphere to exclusively afford (
Z
)-β-boryl-α,β-unsaturated esters.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0034-1380524</doi><tpages>7</tpages></addata></record> |
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title | Copper(II)-Catalyzed β-Borylation of Acetylenic Esters in Water |
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