Deprotonation of benzoxazole and oxazole using lithium magnesates.
about
Chemoselectivity and the curious reactivity preferences of functional groups.Recent advances in direct C-H arylation: Methodology, selectivity and mechanism in oxazole series.Main group multiple C-H/N-H bond activation of a diamine and isolation of a molecular dilithium zincate hydride: experimental and DFT evidence for alkali metal-zinc synergistic effects.One Pot Selective Arylation of 2-Bromo-5-Chloro Thiophene; Molecular Structure Investigation via Density Functional Theory (DFT), X-ray Analysis, and Their Biological Activities.Copper-catalyzed Direct 2-Arylation of Benzoxazoles and Benzoimidazoles with Aryl Bromides and Cytotoxicity of Products.cis-2,6-Dimethylpiperidide: a structural mimic for TMP (2,2,6,6-tetramethylpiperidide) or DA (diisopropylamide)?Developing catalytic applications of cooperative bimetallics: competitive hydroamination/trimerization reactions of isocyanates catalysed by sodium magnesiates.Selective Transformation of Well-Defined Alkenyllithiums to Alkenylmagnesiums via Transmetalation.Iron catalyzed oxidative assembly of N-heteroaryl and aryl metal reagents using oxygen as an oxidant.Isomeric and chemical consequences of the direct magnesiation of 1,3-benzoazoles using β-diketiminate-stabilized magnesium basesMagnesium-Mediated Benzothiazole Activation: A Room-Temperature Cascade of CH Deprotonation, CC Coupling, Ring-Opening, and Nucleophilic Addition ReactionsWalking Down the Chalcogenic Group of the Periodic Table: From Singlet to Triplet Organic Emitters
P2860
Q37655988-5EB4D6E4-8410-4AC7-8369-115F716D7E8EQ39665245-938C45DE-F0D3-4425-B3DC-684C286323C9Q40972504-EB1FD473-8C3E-423E-815A-B9C30A52965EQ41784548-E091E35B-0390-462F-B01E-11C2947E2687Q42318663-AAD9F875-EDBD-4319-AB7C-DFD15D937051Q43214055-5754B6E0-A571-4015-AE7B-84832FAF1129Q45805956-48C761B7-A416-4C52-9A93-5D3EE9031084Q47283753-17EC9876-DF5E-4551-904A-AD3879461974Q50444203-53F862D1-B724-4191-B751-C07A4ADF4FA9Q57966732-589FF5C4-6B49-46D5-862F-74AA4E104659Q57966776-6546B77C-A170-493F-9892-283EEAE250AAQ59132440-05E24F90-2A21-4450-B90F-BBA31573FEB4
P2860
Deprotonation of benzoxazole and oxazole using lithium magnesates.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Deprotonation of benzoxazole and oxazole using lithium magnesates.
@en
Deprotonation of benzoxazole and oxazole using lithium magnesates.
@nl
type
label
Deprotonation of benzoxazole and oxazole using lithium magnesates.
@en
Deprotonation of benzoxazole and oxazole using lithium magnesates.
@nl
prefLabel
Deprotonation of benzoxazole and oxazole using lithium magnesates.
@en
Deprotonation of benzoxazole and oxazole using lithium magnesates.
@nl
P2093
P356
P1476
Deprotonation of benzoxazole and oxazole using lithium magnesates
@en
P2093
Belén Abarca
Christophe Hoarau
Fernando Blanco
Florence Mongin
Francis Marsais
François Trécourt
Guy Quéguiner
Haçan Awad
Laurent Bischoff
P304
P356
10.1021/JO050493W
P407
P577
2005-06-01T00:00:00Z