Palladium- and Nickel-Catalyzed Intramolecular Cyanoboration of Alkynes-Reference-Cited by-同舟云学术

Palladium- and Nickel-Catalyzed Intramolecular Cyanoboration of Alkynes

Published:2003-04-30 Issue:21 Volume:125 Page:6358-6359
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Suginome Michinori¹,Yamamoto Akihiko¹,Murakami Masahiro¹

Affiliation:

1. Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, and PRESTO, Japan Science and Technology Corporation (JST), Sakyo-ku, Kyoto 606-8501, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0349195

Reference13 articles.

1. Activation of Unreactive Bonds and Organic Synthesis

2. Element−Element Addition to Alkynes Catalyzed by the Group 10 Metals

3. Transition-Metal-Catalyzed Additions of Silicon−Silicon and Silicon−Heteroatom Bonds to Unsaturated Organic Molecules

4. Palladium(0)-catalyzed thioboration of terminal alkynes with 9-(alkylthio)-9-borabicyclo[3.3.1]nonane derivatives: stereoselective synthesis of vinyl sulfides via the thioboration-cross-coupling sequence

5. Bis(dialkylamino)cyanoboranes: highly efficient reagents for the Strecker-type aminative cyanation of aldehydes and ketonesElectronic supplementary information (ESI) available: detailed experimental procedures. See http://www.rsc.org/suppdata/cc/b2/b203645b/

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