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A chiral biselectrophile for efficient asymmetric synthesis in water

Hidestål, Olle LU ; Ding, Rui LU ; Almesaker, Ann and Lindström, Ulf LU (2005) In Green Chemistry 7(5). p.259-261
Abstract
The development of an efficient asymmetric dihydroxylation of 1,6-dibromodiene afforded a chiral biselectrophilic diol that displayed highly useful reactivity in water, as demonstrated by a three-step, two-pot asymmetric synthesis of a highly functionalized tetrahydrofuran.
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author
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Green Chemistry
volume
7
issue
5
pages
259 - 261
publisher
Royal Society of Chemistry
external identifiers
  • wos:000228837000004
  • scopus:19744379924
ISSN
1463-9270
DOI
10.1039/b415300f
language
English
LU publication?
yes
additional info
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)
id
eca1c316-9c7d-43db-a38e-c88ff7972662 (old id 152410)
date added to LUP
2016-04-01 12:19:50
date last changed
2022-01-27 02:07:20
@article{eca1c316-9c7d-43db-a38e-c88ff7972662,
  abstract     = {{The development of an efficient asymmetric dihydroxylation of 1,6-dibromodiene afforded a chiral biselectrophilic diol that displayed highly useful reactivity in water, as demonstrated by a three-step, two-pot asymmetric synthesis of a highly functionalized tetrahydrofuran.}},
  author       = {{Hidestål, Olle and Ding, Rui and Almesaker, Ann and Lindström, Ulf}},
  issn         = {{1463-9270}},
  language     = {{eng}},
  number       = {{5}},
  pages        = {{259--261}},
  publisher    = {{Royal Society of Chemistry}},
  series       = {{Green Chemistry}},
  title        = {{A chiral biselectrophile for efficient asymmetric synthesis in water}},
  url          = {{http://dx.doi.org/10.1039/b415300f}},
  doi          = {{10.1039/b415300f}},
  volume       = {{7}},
  year         = {{2005}},
}