About this item
- Title
- A high yielding synthesis of anthranilate esters from sterically hindered alcohols
- Content partner
- The University of Auckland Library
- Collection
- ResearchSpace@Auckland
- Description
A high yielding and operationally simple synthesis of anthranilate esters derived from primary, secondary and tertiary alcohols is reported. Esterification of the alcohol with N-(trifluoroacetyl)anthranilic acid under Steglich conditions, followed by sodium borohydride mediated cleavage of the trifluoroacetyl group affords the anthranilate ester. This new method has application in the synthesis of the ester sidechains of the commonly occurring Delphinium and Aconitum alkaloids and their analo...
- Format
- Research paper
- Research format
- Journal article
- Date created
- 2001-02-26
- Creator
- Barker, David / McLeod, MD / Brimble, MA / Savage, GP
- URL
- http://hdl.handle.net/2292/8012
- Related subjects
- Science & Technology / Physical Sciences / Chemistry, Organic / Chemistry / AE-BICYCLIC ANALOGS / ALKALOID METHYLLYCACONITINE / RECEPTOR ANTAGONIST / LYCOCTONINE / ACYLATION / CATALYSTS / INULINE
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Report this itemDigitalNZ brings together more than 30 million items from institutions so that they are easy to find and use. This information is the best information we could find on this item. This item was added on 22 April 2012, and updated 17 September 2025.
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