dc.contributor.author |
Caprio, VE |
en |
dc.contributor.author |
Jones, MW |
en |
dc.contributor.author |
Brimble, MA |
en |
dc.date.accessioned |
2011-09-21T23:22:00Z |
en |
dc.date.issued |
2001-03 |
en |
dc.identifier.citation |
Molecules 6(3) M200, 2001 |
en |
dc.identifier.issn |
1431-5157 |
en |
dc.identifier.uri |
http://hdl.handle.net/2292/8242 |
en |
dc.description.abstract |
The general part of the experimental section [1] has been presented elsewhere. Di-tert-butyl dicarbonate (3.60 g, 13.2 mmol) and 4-(dimethylamino)pyridine (84 mg, 0.687 mmol) were added to a solution of amine 1 [2] (1.12 g, 13.2 mmol) in acetonitrile (14 mL) under nitrogen at room temperature and stirred for 21 h. The yellow liquid was concentrated under reduced pressure to generate a yellow oil that was purified by flash chromatography using hexane-diethyl ether (3:2) as eluent to afford the title compound 2 (1.77 g, 73%) as a colourless oil. |
en |
dc.relation.ispartofseries |
Molecules |
en |
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/1431-5157/ |
en |
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
en |
dc.rights.uri |
http://creativecommons.org/licenses/by/3.0/ |
en |
dc.title |
tert-Butyl methoxy(2-propynyl)carbamate |
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dc.type |
Journal Article |
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dc.identifier.doi |
10.3390/M200 |
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pubs.issue |
3 |
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pubs.volume |
6 |
en |
dc.rights.holder |
Copyright: 2001 MDPI. |
en |
dc.rights.accessrights |
http://purl.org/eprint/accessRights/OpenAccess |
en |
pubs.subtype |
Article |
en |
pubs.elements-id |
139471 |
en |
pubs.org-id |
Science |
en |
pubs.org-id |
Chemistry |
en |
pubs.org-id |
Science Research |
en |
pubs.org-id |
Maurice Wilkins Centre (2010-2014) |
en |
pubs.record-created-at-source-date |
2013-06-05 |
en |