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protection of a reactive group

Temporary chemical transformation of a reactive group into a group that does not react under conditions where the non-protected group reacts.
Note:
For example, trimethylsilylation is a typical transformation used to protect reactive functional groups, such as hydroxy or amino groups, from their reaction with growing anionic species in anionic polymerization.
Source:
PAC, 2004, 76, 889 (Definitions of terms relating to reactions of polymers and to functional polymeric materials (IUPAC Recommendations 2003)) on page 894
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Cite as:
IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. https://doi.org/10.1351/goldbook.
Last update: 2014-02-24; version: 2.3.3.
DOI of this term: https://doi.org/10.1351/goldbook.PT07148.
Original PDF version: http://www.iupac.org/goldbook/PT07148.pdf. The PDF version is out of date and is provided for reference purposes only. For some entries, the PDF version may be unavailable.
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