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708828 Sigma-Aldrich

2-Thiopheneboronic acid MIDA ester

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Properties

Related Categories Boronic Acids and Derivatives, Chemical Synthesis, Heteroaryl MIDA Boronates, MIDA Boronates, Organometallic Reagents More...
InChI Key   WWELVLHUROSDIA-UHFFFAOYSA-N
mp   189-194 °C

Description

Application

• Reactant for slow-release cross-coupling reactions

MIDA boronates as stable boronic acid surrogates for classically challenging cross-couplings

Suzuki Cross-Coupling with MIDA Boronates

Packaging

1, 5 g in glass bottle

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
1
Protocols & Articles

Articles

MIDA Boronates for Suzuki–Miyaura Cross-Couplings

Professor Martin Burke and coworkers recently prepared retinal using key MIDA building block BB1 in iterative Suzuki-Miyaura cross coupling reactions (Scheme 1). The MIDA unit of BB1 is unreactive un...
Aaron Thornton
ChemFiles Volume 11 Article 1
Keywords: Building blocks, Coupling reactions, Cross couplings, Solvents

Related Content

New MIDA Boronates from Aldrich

MIDA boronates are stable boronic acid surrogates used for Suzuki-Miyaura cross-coupling reactions. These reagents enable the coupling of historically unstable organoboron species; including those co...
Keywords: Aldrichimica Acta, Coupling reactions, Cross couplings, Nuclear magnetic resonance spectroscopy

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