Theoretical investigations of Rh-catalyzed asymmetric 1,4-addition to enones using planar-chiral phosphine-olefin ligands-Reference-Cited by-同舟云学术

Theoretical investigations of Rh-catalyzed asymmetric 1,4-addition to enones using planar-chiral phosphine-olefin ligands

Published:2018-08-24 Issue:1 Volume:40 Page:113-118
ISSN:0192-8651
Container-title:Journal of Computational Chemistry
language:en
Short-container-title:J Comput Chem

Author:

Kawashima Kyohei¹,Sato Takehiro¹,Ogasawara Masamichi²,Kamikawa Ken³,Mori Seiji¹^ORCID

Affiliation:

1. Institute of Quantum Beam Science, Graduate School of Science and Engineering; Ibaraki University; 2-1-1 Bunkyo, Mito, Ibaraki 310-8512 Japan

2. Department of Natural Science, Graduate School of Science and Technology; Tokushima University; 2-1 Minamijousanjimachicho, Tokushima Tokushima 770-8506 Japan

3. Department of Chemistry, Graduate School of Science; Osaka Prefecture University; 1-1 Nakakugakuentyo, Sakai, Osaka 599-8531 Japan

Funder

Japan Society for the Promotion of Science London

Publisher

Wiley

Subject

Computational Mathematics,General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jcc.25550/fullpdf

Reference45 articles.

1. Synthesis of 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of .alpha.-(acylamino)acrylic acids

2. Rhodium-Catalyzed Conjugate Addition of Aryl- or 1-Alkenylboronic Acids to Enones

3. Rhodium-Catalyzed Asymmetric 1,4-Addition of Aryl- and Alkenylboronic Acids to Enones

4. Rhodium-Catalyzed Asymmetric 1,4-Addition and Its Related Asymmetric Reactions

5. Olefins as Steering Ligands for Homogeneously Catalyzed Hydrogenations

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