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9-Anthraldehyde acetals as protecting groups.

Ellervik, Ulf LU (2003) In Tetrahedron Letters 44(11). p.2279-2281
Abstract
Anthraldehyde acetals can be introduced regioselectively to carbohydrates in high yields. Advantages over conventional acetal protecting groups are increased crystallinity and strong absorbance and fluorescence which facilitate purification and reaction monitoring. The anthraldehyde acetals can be deprotected selectively in the presence of benzylidene acetals and can be cleaved regioselectively to yield 6-O-(9-anthracenyl)methyl ethers.
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author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Tetrahedron Letters
volume
44
issue
11
pages
2279 - 2281
publisher
Elsevier
external identifiers
  • wos:000181373500006
  • scopus:0037430424
ISSN
0040-4039
DOI
10.1016/S0040-4039(03)00276-4
language
English
LU publication?
yes
id
0f280ff6-d088-4f5d-aedd-f83ffeb8f38d (old id 127918)
date added to LUP
2007-07-10 09:41:42
date last changed
2017-01-01 06:43:30
@article{0f280ff6-d088-4f5d-aedd-f83ffeb8f38d,
  abstract     = {Anthraldehyde acetals can be introduced regioselectively to carbohydrates in high yields. Advantages over conventional acetal protecting groups are increased crystallinity and strong absorbance and fluorescence which facilitate purification and reaction monitoring. The anthraldehyde acetals can be deprotected selectively in the presence of benzylidene acetals and can be cleaved regioselectively to yield 6-O-(9-anthracenyl)methyl ethers.},
  author       = {Ellervik, Ulf},
  issn         = {0040-4039},
  language     = {eng},
  number       = {11},
  pages        = {2279--2281},
  publisher    = {Elsevier},
  series       = {Tetrahedron Letters},
  title        = {9-Anthraldehyde acetals as protecting groups.},
  url          = {http://dx.doi.org/10.1016/S0040-4039(03)00276-4},
  volume       = {44},
  year         = {2003},
}