期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 57, 期 30, 页码 9465-9469出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201802821
关键词
allylation; asymmetric catalysis; C-H activation; ligand design; palladium
资金
- JST ACT-C [JPMJCR12YN]
- JSPS KAKENHI [JP15H05801]
- JSPS
The palladium-catalyzed asymmetric side-chain C(alpha)-allylation of 2-alkylpyridines, without using an external base, was developed. The high linear selectivities and enantioselectivities were achieved using new chiral diamidophosphite monodentate ligands. Given that the reaction conditions do not require an external base, this catalyst system enabled chemoselective C(alpha)-allylation of 2-alkylpyridines containing alpha-carbonyl C-H bonds, which are more acidic than alpha-pyridyl C-H bonds.
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