Opposite Regiospecific Ring Opening of 2-(Cyanomethyl)aziridines by Hydrogen Bromide and Benzyl Bromide: Experimental Study and Theoretical Rationalization-Reference-Cited by-同舟云学术

Opposite Regiospecific Ring Opening of 2-(Cyanomethyl)aziridines by Hydrogen Bromide and Benzyl Bromide: Experimental Study and Theoretical Rationalization

Published:2010-05-27 Issue:13 Volume:75 Page:4530-4541
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Catak Saron¹²,D’hooghe Matthias³,Verstraelen Toon¹²,Hemelsoet Karen¹²,Van Nieuwenhove Andries³,Ha Hyun-Joon⁴,Waroquier Michel¹²,De Kimpe Norbert³,Van Speybroeck Veronique¹²

Affiliation:

1. Center for Molecular Modeling, Ghent University, Technologiepark 903, B-9052 Zwijnaarde, Belgium

2. QCMM-Alliance, Ghent-Brussels, Belgium

3. Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium

4. Department of Chemistry and Protein Research Center for Bio-Industry, Hankuk University of Foreign Studies, Yongin 449-791, Korea

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo100687q

Reference111 articles.

1. Aminolysis of Vinyl Epoxides as an Efficient Entry to N-H Vinylaziridines

2. The Synthetic Potential of Three-Membered Ring Aza-Heterocycles

3. Aziridines: epoxides’ ugly cousins?

4. Nucleophilic ring opening of aziridines

5. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations

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