Internal Delivery of Soft Chlorine and Bromine Atoms: Stereoselective Synthesis of (E)-β-Halogenovinyl(aryl)-λ3-iodanes through Domino λ3-Iodanation−1,4-Halogen Shift−Fluorination of Alkynes-Reference-Cited by-同舟云学术

Internal Delivery of Soft Chlorine and Bromine Atoms: Stereoselective Synthesis of (E)-β-Halogenovinyl(aryl)-λ3-iodanes through Domino λ3-Iodanation−1,4-Halogen Shift−Fluorination of Alkynes

Published:2007-07-21 Issue:17 Volume:9 Page:3335-3338
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ochiai Masahito¹,Hirobe Masaya¹,Yoshimura Akira¹,Nishi Yoshio¹,Miyamoto Kazunori¹,Shiro Motoo¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, University of Tokushima, 1-78 Shomachi, Tokushima 770-8505, Japan, and Rigaku Corporation, 3-9-12 Matsubara, Akishima, Tokyo 196-8666, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol071345q

Reference36 articles.

1. Reactivities, Properties and Structures

2. Recent Developments in the Chemistry of Polyvalent Iodine Compounds

3. Halonium Ions

4. Solvolysis of Cyclohexenyliodonium Salt, a New Precursor for the Vinyl Cation: Remarkable Nucleofugality of the Phenyliodonio Group and Evidence for Internal Return from an Intimate Ion-Molecule Pair

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