Affiliation:
1. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, Russia
2. Drug Control Centre, King's College London, Franklin-Wilkins Building, Stamford Street, London SE1 9NN, UK
Abstract
The present review is devoted to acylation as a widely employed derivatization procedure for protection of OH (alcohols, polyols, phenols, enols), SH (thiols) and NH (amines, amides) groups in order to increase volatility, improve chromatographic properties and, if possible, improve mass spectral properties of derivatives. Chemical aspects of derivatization and various acylating agents are characterized. Mass spectral [electron ionization (EI), chemical ionization (CI) and negative-ion (NI) CI] properties of derivatives that are helpful in identification, structure elucidation and quantitative determination of the analyzed compounds are discussed. Some recent analytical applications of the procedure in synthetic organic chemistry, clinical chemistry, environmental chemistry etc. are summarized.
Subject
Spectroscopy,Atomic and Molecular Physics, and Optics,General Medicine
Cited by
61 articles.
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