The Mechanism of 1,4 Alkyl Group Migration in Hypervalent Halonium Ylides: The Stereochemical Course-Reference-Cited by-同舟云学术

The Mechanism of 1,4 Alkyl Group Migration in Hypervalent Halonium Ylides: The Stereochemical Course

Published:2008-05-21 Issue:24 Volume:130 Page:7564-7565
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Moriarty Robert M.¹,Tyagi Sachin¹,Ivanov Daniela¹,Constantinescu Mircea¹

Affiliation:

1. Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061, “P. Poni” Institute of Macromolecular Chemistry, 41A Gr. Ghica Voda Alley, 700 487 Iaşi, România, and Department of Chemistry, “Al. I. Cuza” University, Faculty of Chemistry, 11 Carol Boulevard, 700 506 Iaşi, România

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja802735f

Reference38 articles.

1. Stable carbonium ions. XLVIII. Halonium ion formation via neighboring halogen participation. Tetramethylethylene halonium ions

2. Friedel-Crafts chemistry. V. Isolation, carbon-13 nuclear magnetic resonance, and laser Raman spectroscopic study of dimethylhalonium fluoroantimonates

3. Heterolytic decomposition of onium compounds (diphenyl halogenonium and triphenyloxonium salts)

4. eKoser, G. F.The Chemistry of Halides, Pseudo-halides and Azides;Wiley-Interscience:Chichester, U.K. 1983; p721.

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