Metal-Controlled Reactivity of a Pincer-type, σ-Coordinated Naphthyl Radical Anion-Reference-Cited by-同舟云学术

Metal-Controlled Reactivity of a Pincer-type, σ-Coordinated Naphthyl Radical Anion

Published:2006-05-16 Issue:22 Volume:128 Page:7128-7129
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Frech Christian M.¹,Ben-David Yehoshoa¹,Weiner Lev¹,Milstein David¹

Affiliation:

1. Department of Organic Chemistry and Unit of Chemical Research Support, Weizmann Institute of Science, 76100 Rehovot, Israel, and Department of Inorganic Chemistry, University of Zurich, 8057 Zurich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0615066

Reference17 articles.

1. Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers

2. 1,3-Bis(phenylmercapto)propane and 1-chloro-3-(phenylmercapto)propane: useful precursors for 1,3-dilithiopropane synthons in the preparation of 1,5-diols

3. Generation, some synthetic uses, and 1,2-vinyl rearrangements of secondary and tertiary homoallyllithiums, including ring contractions and a ring expansion. Remarkable acceleration of the rearrangement by an oxyanionic group

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