Journal article
A reliable synthesis of 2- and 6-amino-β-cyclodextrin and permethylated-β-cyclodextrin
Tetrahedron Letters, Vol.46(46), pp.7905-7907
2005
Abstract
A new, reliable method for the introduction of an amine group at positions 2 or 6 of β-cyclodextrin and permethyl-β-cyclodextrin is described. It involves selective tosylation followed by azide substitution and almost quantitative reduction with triphenylphosphine followed by hydrolysis of the phosphinimine intermediate. © 2005 Elsevier Ltd. All rights reserved.
Details
- Title
- A reliable synthesis of 2- and 6-amino-β-cyclodextrin and permethylated-β-cyclodextrin
- Authors
- I W Muderawan (Author) - Nanyang Technological University, SingaporeT T Ong (Author) - Institute of Chemical and Engineering Sciences, SingaporeC L Teck (Author) - Nanyang Technological University, SingaporeDavid James Young (Author) - Griffith UniversityB C Chi (Author) - Nanyang Technological University, SingaporeS C Ng (Author) - Griffith University
- Publication details
- Tetrahedron Letters, Vol.46(46), pp.7905-7907
- Publisher
- Pergamon
- Date published
- 2005
- DOI
- 10.1016/j.tetlet.2005.09.099
- ISSN
- 0040-4039
- Organisation Unit
- University of the Sunshine Coast, Queensland
- Language
- English
- Record Identifier
- 99449934202621
- Output Type
- Journal article
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- Chemistry, Organic
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