Organocatalytic Diboration Involving “Reductive Addition” of a Boron–Boron σ-Bond to 4,4′-Bipyridine-Reference-Cited by-同舟云学术

Organocatalytic Diboration Involving “Reductive Addition” of a Boron–Boron σ-Bond to 4,4′-Bipyridine

Published:2015-02-19 Issue:8 Volume:137 Page:2852-2855
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Ohmura Toshimichi¹,Morimasa Yohei¹,Suginome Michinori¹

Affiliation:

1. Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.5b00546

Reference65 articles.

1. The Handbook of Homogeneous Hydrogenation

2. Element−Element Additions to Unsaturated Carbon−Carbon Bonds Catalyzed by Transition Metal Complexes

3. Catalytic enantioselective diboration, disilation and silaboration: new opportunities for asymmetric synthesis

4. Silylboranes as New Tools in Organic Synthesis

5. dSuginome, M.; Ohmura, T.InBoronic Acids,2nded.Hall, D., Ed.Wiley-VCH: 2011; Vol.1, p171.

Cited by 62 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Uncatalyzed Diboron Activation by a Strained Hydrocarbon: Experimental and Theoretical Study of [1.1.1]Propellane Diborylation;Chemistry – A European Journal;2024-08-30

2. Ligand-Enabled Regio- and/or Stereoselective Hydroboration of Alkenes;Synlett;2023-05-31

3. Water‐Soluble Fe(II) Complexes for Theranostic Application: Synthesis, Photoacoustic Imaging, and Photothermal Conversion;European Journal of Inorganic Chemistry;2023-05-25

4. Bis(neopentylglycolato)diboron (B₂nep₂) as a bidentate ligand and a reducing agent for early transition metal chlorides giving MCl₄(B₂nep₂) complexes;Dalton Transactions;2023

5. Multiple stable redox states and tunable ground states via the marriage of viologens and Chichibabin's hydrocarbon;Chemical Science;2023