Regioselectivity in the ring opening of non-activated aziridines-Reference-Cited by-同舟云学术

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Regioselectivity in the ring opening of non-activated aziridines

Published:2012 Issue:2 Volume:41 Page:643-665
ISSN:0306-0012
Container-title:Chem. Soc. Rev.
language:en
Short-container-title:Chem. Soc. Rev.

Author:

Stanković Sonja,D'hooghe Matthias,Catak Saron,Eum Heesung,Waroquier Michel,Van Speybroeck Veronique,De Kimpe Norbert,Ha Hyun-Joon

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/CS/C1CS15140A

Reference117 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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2. Nickel-Catalyzed Enantioselective C(sp³)–C(sp³) Cross-Electrophile Coupling of N-Sulfonyl Styrenyl Aziridines with Alkyl Bromides;Journal of the American Chemical Society;2024-09-04

3. Synthesis of 2‐Aminopyridine Derivatives via a Tandem CuAAC/Ring‐Cleavage/[4+2]‐Cycloaddition/Rearrangement Reaction Sequence;Advanced Synthesis & Catalysis;2024-08-07

4. Copolymerization of Isothiocyanates and Nonactivated Aziridines Mediated by Zwitterionic Intermediates through Condensation and Chain Growth;Macromolecules;2024-08-06

5. Nonactivated Aziridine Synthesis by Intermolecular Polarity-Mismatched Carboamination of Unactivated Alkenes with Unactivated Alkyl Halides;Organic Letters;2024-07-01

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