期刊
SYNLETT
卷 32, 期 15, 页码 1484-1491出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/a-1503-6330
关键词
nickel catalysis; cross-coupling; oxidative addition; chemoselectivity; density functional theory; Suzuki-Miyaura coupling
资金
- National Science Foundation [CAREER: CHE-1848090, CHE-170089, ACI-1548562]
The chemoselective cross-coupling of phenol derivatives is valuable for synthesizing products with retained halides. This review focuses on recent developments in selective cross-couplings of chloroaryl phenol derivatives, particularly reactions involving chloroaryl tosylates. A detailed discussion is provided on the first example of a C-O-selective Ni-catalyzed Suzuki-Miyaura coupling of chloroaryl tosylates.
Chemoselective cross-coupling of phenol derivatives is valuable for generating products that retain halides. Here we discuss recent developments in selective cross-couplings of chloroaryl phenol derivatives, with a particular focus on reactions of chloroaryl tosylates. The first example of a C-O-selective Ni-catalyzed Suzuki-Miyaura coupling of chloroaryl tosylates is discussed in detail.
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