4.8 Article

Design, Generation, and Synthetic Application of Borylzincate: Borylation of Aryl Halides and Borylzincation of Benzynes/Terminal Alkyne

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 50, Pages 18730-18733

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja409748m

Keywords

-

Funding

  1. JSPS KAKENHI [24229011]
  2. Takeda Science Foundation
  3. Asahi Glass Foundation
  4. Daiichi-Sankyo Foundation of Life Sciences
  5. Mochida Memorial Foundation
  6. Tokyo Biochemical Research Foundation
  7. Foundation NAGASE Science Technology Development
  8. Yamada Science Foundation
  9. Sumitomo Foundation
  10. JSPS [25713001, 24850005]
  11. Grants-in-Aid for Scientific Research [25713001, 24850005] Funding Source: KAKEN

Ask authors/readers for more resources

Borylzincate was generated in situ from dialkylzinc, diboron, and metal alkoxide. Model DFT calculations showed that although the formation of borylzincate is kinetically favorable, it is thermodynamically unfavorable. Therefore, we designed a successive reaction sequence that would provide a compensating energy gain. This enabled Zn-catalyzed borylation of aryl halides and borylzincation of benzynes and terminal alkyne from diborons without the need for any cocatalyst.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available