Nickel-catalyzed coupling reaction of lithium organoborates and aryl mesylates possessing an electron withdrawing group

102Citations
Citations of this article
15Readers
Mendeley users who have this article in their library.
Get full text

Abstract

In the presence of NiCl2(PPh3)2 as catalyst, p-methoxycarbonylphenyl mesylate (5) and tosylate (6) react with lithium arylborates 4 (Ar = 2-furyl, Ph, p-Me-Ph, p-MeO-Ph) at room temperature to afford the coupling products in high yields. Similarly, mesylates 9-11 coupled with these borates 4 efficiently.

References Powered by Scopus

Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

12564Citations
N/AReaders
Get full text

The Palladium-Catalyzed Cross-Coupling Reaction Of Phenylboronic Acid With Haloarenes In The Presence Of Bases

1963Citations
N/AReaders
Get full text

Palladium-Catalyzed Coupling of Aryl Triflates with Organostannanes

675Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Recent applications of the Suzuki-Miyaura cross-coupling reaction in organic synthesis

1812Citations
N/AReaders
Get full text

Nickel-catalyzed cross-couplings involving carbon-oxygen bonds

1238Citations
N/AReaders
Get full text

Catalytic cross-coupling reactions in biaryl synthesis

1071Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Kobayashi, Y., & Mizojiri, R. (1996). Nickel-catalyzed coupling reaction of lithium organoborates and aryl mesylates possessing an electron withdrawing group. Tetrahedron Letters, 37(47), 8531–8534. https://doi.org/10.1016/0040-4039(96)01984-3

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 4

40%

Researcher 4

40%

Professor / Associate Prof. 1

10%

Lecturer / Post doc 1

10%

Readers' Discipline

Tooltip

Chemistry 9

90%

Biochemistry, Genetics and Molecular Bi... 1

10%

Save time finding and organizing research with Mendeley

Sign up for free