✦ LIBER ✦

Practical Copper-Catalyzed Asymmetric Synthesis of Chiral Chrysanthemic Acid Esters

✍ Scribed by Itagaki, Makoto; Suenobu, Katsuhiro

Book ID: 127200695
Publisher: American Chemical Society
Year: 2007
Tongue: English
Weight: 249 KB
Volume: 11
Category: Article
ISSN: 1083-6160
DOI: 10.1021/op060238t

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Practical Copper-Catalyzed Asymmetric Sy

Practical Copper-Catalyzed Asymmetric Synthesis of Chiral Chrysanthemic Acid Esters

✍ Makoto Itagaki; Katsuhiro Suenobu 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 11 KB 👁 1 views

Copper-Catalyzed Asymmetric Synthesis of

Copper-Catalyzed Asymmetric Synthesis of Chiral Allylic Esters.

✍ Koen Geurts; Stephen P. Fletcher; Ben L. Feringa 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

Copper Catalyzed Asymmetric Synthesis of

Copper Catalyzed Asymmetric Synthesis of Chiral Allylic Esters

✍ Geurts, Koen; Fletcher, Stephen P.; Feringa, Ben L. 📂 Article 📅 2006 🏛 American Chemical Society 🌐 English ⚖ 52 KB

Copper-Catalyzed Asymmetric Synthesis (A

Copper-Catalyzed Asymmetric Synthesis (Alexakis/Copper-Catalyzed Asymmetric Synthesis) || Chiral Copper Lewis Acids in Asymmetric Transformations

✍ Alexakis, Alexandre; Krause, Norbert; Woodward, Simon 📂 Article 📅 2014 🏛 Wiley-VCH Verlag GmbH & Co. KGaA ⚖ 404 KB

Asymmetric synthesis of chrysanthemic ac

Asymmetric synthesis of chrysanthemic acid. An application of copper carbenoid reaction

✍ T. Aratani; Y. Yoneyoshi; T. Nagase 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 198 KB

Chrysanthemic acid (I, R = H) constitutes an acidic component of the pyrethroid, 1 which is effective as an insecticide. Among its four optical isomers, the naturally occurring d-trans isomer has the highest activity.

Asymmetric synthesis of chrysanthemic ac

Asymmetric synthesis of chrysanthemic acid. An application of copper carbenoid reaction

✍ T. Aratani; Y. Yoneyoshi; T. Nagase 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 176 KB

Asymmetric induction was observed in the decomposition of diasoalkanes in the presence of certain chiral copper complexes. 1 We have applied this chiral carbenoid reaction to the synthesis of chrysanthemic acid\* (ea. 1). Systematic studies have been carried out to achieve an optical yield of 60-70$