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Updated: Jan 26, 2026

Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores
Published on: August 19, 2013
Virtues of Volatility: A Facile Transesterification Approach to Boronic Acids
Stefan P A Hinkes1, Christian D P Klein1
1Institute of Pharmacy and Molecular Biotechnology (IPMB), Medicinal Chemistry , University of Heidelberg , Im Neuenheimer Feld 364 , 69120 Heidelberg , Germany.
Abstract:
Boronic acids are an increasingly important compound class for many applications, including C-C bond formation reactions, medicinal chemistry, and diagnostics. The deprotection of boronic ester intermediates is frequently a problematic and inefficient step in boronic acid syntheses. We describe an approach that highly facilitates this transformation by leveraging the volatility of methylboronic acid and its diol esters. The method is performed under mild conditions, provides high yields, and eliminates cumbersome and problematic purification steps.
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