C1-Symmetric Binap Derivative Featuring Single Diferrocenylphosphino-Donor Moiety-Reference-Cited by-同舟云学术

C1-Symmetric Binap Derivative Featuring Single Diferrocenylphosphino-Donor Moiety

Published:2021-04-09 Issue:8 Volume:40 Page:1020-1024
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Enomoto Yuuki¹,Ichiryu Hiroki¹,Hu Hao¹²,Ura Yasuyuki³^ORCID,Ogasawara Masamichi¹^ORCID

Affiliation:

1. Department of Natural Science, Graduate School of Science and Technology, Tokushima International Science Institute, and Research Cluster on “Innovative Chemical Sensing”, Tokushima University, Tokushima 770-8506, Japan

2. Graduate School of Life Science, Hokkaido University, Kita-ku, Sapporo 001-0021, Japan

3. Department of Chemistry, Biology, and Environmental Science, Faculty of Science, Nara Women’s University, Kitauoyanishi-machi, Nara 630-8506, Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.1c00132

Reference29 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. Palladium-catalyzed asymmetric arylation of 2,3-dihydrofuran with phenyl triflate. A novel asymmetric catalysis involving a kinetic resolution process

3. Modified BINAP: The How and the Why

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