A New Route to Methyl (R,E)-(−)-Tetradeca-2,4,5-trienoate (Pheromone of Acanthoscelides obtectus) Utilizing a Palladium-Catalyzed Asymmetric Allene Formation Reaction-Reference-Cited by-同舟云学术

A New Route to Methyl (R,E)-(−)-Tetradeca-2,4,5-trienoate (Pheromone of Acanthoscelides obtectus) Utilizing a Palladium-Catalyzed Asymmetric Allene Formation Reaction

Published:2005-06-08 Issue:14 Volume:70 Page:5764-5767
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ogasawara Masamichi¹,Nagano Takashi¹,Hayashi Tamio¹

Affiliation:

1. Catalysis Research Center and Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita-ku, Sapporo 001-0021, Japan, and Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan ogasawar@cat.hokudai.ac.jp; thayashi@kuchem.kyoto-u.ac.jp

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo050684z

Reference31 articles.

1. π-Allylpalladium-Mediated Catalytic Synthesis of Functionalized Allenes

2. Chloroprene as a Source of Fine Chemicals: Palladium-Catalyzed Synthesis of Terminal Allenes

3. Preparation of Multisubstituted Allenes from Allylsilanes

4. Palladium-Catalyzed Asymmetric Synthesis of Axially Chiral Allenes: A Synergistic Effect of Dibenzalacetone on High Enantioselectivity

5. Palladium-Catalyzed Asymmetric Synthesis of Axially Chiral (Allenylmethyl)silanes and Chirality Transfer to Stereogenic Carbon Centers in SE‘ Reactions

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