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Abstract

The Suzuki-Miyaura cross-coupling of 3,4-disubstituted 5-bromoisoxazoles 1 at the C5 position has successfully proceeded in the presence of Pd-2(dba)(3) and P(t-Bu)(3)center dot HBF4 catalysts to give the corresponding trisubstituted isoxazoles 3 in good to high yields while suppressing the formation of ketone 4 as a byproduct. The use of bulky phosphine ligand P(t-Bu)(3)center dot HBF4 is essential for the current transformation, and the formation of ketone 4, which was a major product in the previous report, was able to be suppressed under the current conditions. (C) 2021 Elsevier Ltd. All rights reserved.

Authors

Tsuda, Masato;  Morita, Taiki;  Nakamura, Hiroyuki

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