Tert-Butyldimethylsilyl Amine (TBDMS-NH2): A Mild and Green Reagent for the Protection of Benzyl Alcohols, Phenols, and Carboxylic Acids under Solvent-Free Conditions

Duczynski, J.; Fuller, Rebecca; Stewart, S.

doi:10.1071/CH16097

dc.contributor.author	Duczynski, J.
dc.contributor.author	Fuller, Rebecca
dc.contributor.author	Stewart, S.
dc.date.accessioned	2018-06-29T12:26:10Z
dc.date.available	2018-06-29T12:26:10Z
dc.date.created	2018-06-29T12:08:56Z
dc.date.issued	2016
dc.identifier.citation	Duczynski, J. and Fuller, R. and Stewart, S. 2016. Tert-Butyldimethylsilyl Amine (TBDMS-NH2): A Mild and Green Reagent for the Protection of Benzyl Alcohols, Phenols, and Carboxylic Acids under Solvent-Free Conditions. Australian Journal of Chemistry. 69 (10): pp. 1172-1179.
dc.identifier.uri	http://hdl.handle.net/20.500.11937/68534
dc.identifier.doi	10.1071/CH16097
dc.description.abstract	© The Authors 2016. Herein, we present the use of the tert-butyldimethylsilyl amine (TBDMS-NH2) as a silylating reagent for phenols, benzyl alcohols, and carboxylic acids. Unlike other silyl protection reactions, this reported process with TBDMS-NH2 does not involve the formation of HCl. Importantly, we report the efficacy of this reagent in operating under solvent-free conditions and enabling short reaction times.
dc.publisher	CSIRO Publishing
dc.title	Tert-Butyldimethylsilyl Amine (TBDMS-NH2): A Mild and Green Reagent for the Protection of Benzyl Alcohols, Phenols, and Carboxylic Acids under Solvent-Free Conditions
dc.type	Journal Article
dcterms.source.volume	69
dcterms.source.number	10
dcterms.source.startPage	1172
dcterms.source.endPage	1179
dcterms.source.issn	0004-9425
dcterms.source.title	Australian Journal of Chemistry
curtin.department	School of Molecular and Life Sciences (MLS)
curtin.accessStatus	Fulltext not available

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