Ghent University Academic Bibliography

Advanced

Regioselectivity in the ring opening of non-activated aziridines

Sonja Stanković UGent, Matthias D'hooghe UGent, Saron Catak UGent, Heesung Eum, Michel Waroquier UGent, Veronique Van Speybroeck UGent, Norbert De Kimpe UGent and Hyun-Joon Ha (2012) CHEMICAL SOCIETY REVIEWS. 41(2). p.643-665
abstract
In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate aziridinium salts will be dealt with. Emphasis will be put on the relationship between the observed regioselectivity and inherent structural features such as the nature of the C2 aziridine substituent and the nature of the electrophile and the nucleophile. This overview should allow chemists to gain insight into the factors governing the regioselectivity in aziridinium ring openings (81 references).
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (review)
publication status
published
subject
keyword
BETA-AMINO ALCOHOLS, CHIRAL AZIRIDINES, AROMATIC-AMINES, CARBOXYLIC-ACIDS, THEORETICAL RATIONALIZATION, CONTAINING HETEROCYCLES, ASYMMETRIC-SYNTHESIS, EFFICIENT SYNTHESIS, STEREOSELECTIVE-SYNTHESIS, ENANTIOMERICALLY PURE
journal title
CHEMICAL SOCIETY REVIEWS
Chem. Soc. Rev.
volume
41
issue
2
pages
643 - 665
Web of Science type
Review
Web of Science id
000298854900010
JCR category
CHEMISTRY, MULTIDISCIPLINARY
JCR impact factor
24.892 (2012)
JCR rank
2/150 (2012)
JCR quartile
1 (2012)
ISSN
0306-0012
DOI
10.1039/c1cs15140a
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
2017476
handle
http://hdl.handle.net/1854/LU-2017476
date created
2012-02-03 09:36:30
date last changed
2012-03-07 15:20:37
@article{2017476,
  abstract     = {In this critical review, the ring opening of non-activated 2-substituted aziridines via intermediate aziridinium salts will be dealt with. Emphasis will be put on the relationship between the observed regioselectivity and inherent structural features such as the nature of the C2 aziridine substituent and the nature of the electrophile and the nucleophile. This overview should allow chemists to gain insight into the factors governing the regioselectivity in aziridinium ring openings (81 references).},
  author       = {Stankovi\'{c}, Sonja and D'hooghe, Matthias and Catak, Saron and Eum, Heesung and Waroquier, Michel and Van Speybroeck, Veronique and De Kimpe, Norbert and Ha, Hyun-Joon},
  issn         = {0306-0012},
  journal      = {CHEMICAL SOCIETY REVIEWS},
  keyword      = {BETA-AMINO ALCOHOLS,CHIRAL AZIRIDINES,AROMATIC-AMINES,CARBOXYLIC-ACIDS,THEORETICAL RATIONALIZATION,CONTAINING HETEROCYCLES,ASYMMETRIC-SYNTHESIS,EFFICIENT SYNTHESIS,STEREOSELECTIVE-SYNTHESIS,ENANTIOMERICALLY PURE},
  language     = {eng},
  number       = {2},
  pages        = {643--665},
  title        = {Regioselectivity in the ring opening of non-activated aziridines},
  url          = {http://dx.doi.org/10.1039/c1cs15140a},
  volume       = {41},
  year         = {2012},
}

Chicago
Stanković, Sonja, Matthias D’hooghe, Saron Catak, Heesung Eum, Michel Waroquier, Veronique Van Speybroeck, Norbert De Kimpe, and Hyun-Joon Ha. 2012. “Regioselectivity in the Ring Opening of Non-activated Aziridines.” Chemical Society Reviews 41 (2): 643–665.
APA
Stanković, Sonja, D’hooghe, M., Catak, S., Eum, H., Waroquier, M., Van Speybroeck, V., De Kimpe, N., et al. (2012). Regioselectivity in the ring opening of non-activated aziridines. CHEMICAL SOCIETY REVIEWS, 41(2), 643–665.
Vancouver
1.
Stanković S, D’hooghe M, Catak S, Eum H, Waroquier M, Van Speybroeck V, et al. Regioselectivity in the ring opening of non-activated aziridines. CHEMICAL SOCIETY REVIEWS. 2012;41(2):643–65.
MLA
Stanković, Sonja, Matthias D’hooghe, Saron Catak, et al. “Regioselectivity in the Ring Opening of Non-activated Aziridines.” CHEMICAL SOCIETY REVIEWS 41.2 (2012): 643–665. Print.