Design, Generation, and Synthetic Application of Borylzincate: Borylation of Aryl Halides and Borylzincation of Benzynes/Terminal Alkyne-Reference-Cited by-同舟云学术

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

Published:2013-12-10 Issue:50 Volume:135 Page:18730-18733
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Nagashima Yuki¹,Takita Ryo¹,Yoshida Kengo²,Hirano Keiichi¹,Uchiyama Masanobu¹²

Affiliation:

1. Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

2. Advanced Elements Chemistry Research Team, RIKEN Center for Sustainable Resource Science, and Elements Chemistry Laboratory, RIKEN, 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja409748m

Reference43 articles.

1. New Formulas for Organozincate Chemistry

2. Toward a Protecting-Group-Free Halogen−Metal Exchange Reaction: Practical, Chemoselective Metalation of Functionalized Aromatic Halides Using Dianion-type Zincate, tBu4ZnLi2

3. Aryl Ether as a Negishi Coupling Partner: An Approach for Constructing CC Bonds under Mild Conditions

4. Design, Reactivities, and Practical Application of Dialkylzinc Hydride Ate Complexes Generated in Situ from Dialkylzinc and Metal Hydride. A New Methodology for Activation of NaH and LiH under Mild Conditions

5. TMP−Zincate as Highly Chemoselective Base for Directed Ortho Metalation

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