<i>N</i>,<i>N</i>-Disubstituted Allylic Amine Type Aminophosphines with C(aryl)–N(amine) Bond Axial Chirality: Synthesis and Application to Palladium-Catalyzed Asymmetric Allylic Alkylation with Malonates-Reference-Cited by-同舟云学术

N,N-Disubstituted Allylic Amine Type Aminophosphines with C(aryl)–N(amine) Bond Axial Chirality: Synthesis and Application to Palladium-Catalyzed Asymmetric Allylic Alkylation with Malonates

Published:2018 Issue:10 Volume:67 Page:1189-1199
ISSN:1345-8957
Container-title:Journal of Oleo Science
language:en
Short-container-title:J. Oleo Sci.

Author:

Mino Takashi¹²,Youda Junpei¹,Ebisawa Toshibumi¹,Shima Yamato¹,Nishikawa Kenji¹,Yoshida Yasushi¹²,Sakamoto Masami¹²

Affiliation:

1. Graduate School of Engineering, Chiba University

2. Molecular Chirality Research Center, Chiba University

Publisher

Japan Oil Chemists' Society

Subject

General Chemical Engineering,General Medicine,General Chemistry

Link

https://www.jstage.jst.go.jp/article/jos/67/10/67_ess17260/_pdf

Reference41 articles.

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2. 2) Ager, D.J.; de Vries, A.H.M.; de Vries, J.G. Asymmetric homogeneous hydrogenations at scale. Chem. Soc. Rev. 41, 3340-3380 (2012).

3. 3) Busacca, C.A.; Fandrick, D.R.; Song, J.J.; Senanayake, C.H. The growing impact of catalysis in the pharmaceutical industry. Adv. Synth. Catal. 353, 1825-1864 (2011).

4. 4) Helmchen, G.; Pfaltz, A. Phosphinooxazolines – a new class of versatile, modular P,N-ligands for asymmetric catalysis. Acc. Chem. Res. 33, 336-345 (2000).

5. 5) Pfaltz, A. From corrin chemistry to asymmetric catalysis - a personal account. Synlett 835-842 (1999).

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