Synthesis and Characterization of β-Haloalkenyl-λ3-bromanes: Stereoselective Markovnikov Addition of Difluoro(aryl)-λ3-bromane to Terminal Acetylenes-Reference-Cited by-同舟云学术

Synthesis and Characterization of β-Haloalkenyl-λ3-bromanes: Stereoselective Markovnikov Addition of Difluoro(aryl)-λ3-bromane to Terminal Acetylenes

Published:2005-07-07 Issue:30 Volume:127 Page:10460-10461
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ochiai Masahito¹,Nishi Yoshio¹,Mori Takeshi¹,Tada Norihiro¹,Suefuji Takashi¹,Frohn Hermann J.¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, University of Tokushima, 1-78 Shomachi, Tokushima 770-8505, Japan, and Anorganische Chemie, Universitat Duisburg-Essen, Lotharstrasse 1, D-47048 Duisburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja051690f

Reference15 articles.

1. 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

2. Nucleophilic vinylic substitutions of λ3-vinyliodanes

3. Inversion of configuration in nucleophilic vinylic substitutions of (E)-.beta.-alkylvinyliodonium tetrafluoroborates with halides

4. In-Plane Vinylic SN2 Substitution and Intramolecular β Elimination of β-Alkylvinyl(chloro)-λ3-iodanes

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