Regioselectivity in the ring opening of non-activated aziridines
(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:
http://hdl.handle.net/1854/LU-2017476
- author
- 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
- organization
- year
- 2012
- 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.