Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to SN1 and SN2 Processes.
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Enantioselective Construction of Trifluoromethoxylated Stereogenic Centers by a Nickel-Catalyzed Asymmetric Suzuki-Miyaura Coupling of Secondary Benzyl Bromides.Transition-Metal-Free Radical C(sp3)-C(sp2) and C(sp3)-C(sp3) Coupling Enabled by 2-Azaallyls as Super-Electron-Donors and Coupling-Partners.Ni-Catalyzed Electrochemical Decarboxylative C-C Couplings in Batch and Continuous Flow.Nickel-Catalyzed Enantioconvergent Borylation of Racemic Secondary Benzylic ElectrophilesChromium-catalyzed para-selective formation of quaternary carbon centers by alkylation of benzamide derivativesIntermolecular selective carboacylation of alkenes via nickel-catalyzed reductive radical relayKupferkatalysierte decarboxylierende radikalische Silylierung von redoxaktiven aliphatischen Carbonsäurederivaten
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P2860
Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to SN1 and SN2 Processes.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Transition-Metal Catalysis of ...... tive to SN1 and SN2 Processes.
@en
type
label
Transition-Metal Catalysis of ...... tive to SN1 and SN2 Processes.
@en
prefLabel
Transition-Metal Catalysis of ...... tive to SN1 and SN2 Processes.
@en
P2860
P1433
P1476
Transition-Metal Catalysis of ...... tive to SN1 and SN2 Processes.
@en
P2093
Gregory C Fu
P2860
P304
P356
10.1021/ACSCENTSCI.7B00212
P577
2017-06-12T00:00:00Z