dehydrogenative coupling;
heteroarenes;
manganese;
olefination;
pincer ligands;
ASYMMETRIC TRANSFER HYDROGENATION;
C BOND FORMATION;
SUSTAINABLE SYNTHESIS;
PINCER COMPLEXES;
STYRYL DYES;
AMINES;
DEHYDROGENATION;
ALKYLATION;
KETONES;
IRON;
D O I:
10.1002/anie.201804729
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Herein, we present the first catalytic direct olefination of methyl-substituted heteroarenes with primary alcohols through an acceptorless dehydrogenative coupling. The reaction is catalyzed by a complex of the earth-abundant transition metal manganese that is stabilized by a bench-stable NNN pincer ligand derived from 2-hydrazinylpyridine. The reaction is environmentally benign, producing only hydrogen and water as byproducts. A large number of E-disubstituted olefins were selectively obtained with high efficiency.
机构:
Nagoya Univ, Inst Transformat Biomol WPI ITbM, Grad Sch Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
Nagoya Univ, Dept Chem, Grad Sch Sci, Chikusa Ku, Nagoya, Aichi 4648602, JapanNagoya Univ, Inst Transformat Biomol WPI ITbM, Grad Sch Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
Hattori, Keika
Ziadi, Asraa
论文数: 0引用数: 0
h-index: 0
机构:
Nagoya Univ, Inst Transformat Biomol WPI ITbM, Grad Sch Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
Nagoya Univ, Dept Chem, Grad Sch Sci, Chikusa Ku, Nagoya, Aichi 4648602, JapanNagoya Univ, Inst Transformat Biomol WPI ITbM, Grad Sch Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan