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1 zed with 5-amino-2-naphthalenesulfonic acid (ANSA).
3 valent of FeCl2 produced the hybrid complex, ansa-(2-(CH2)2)-(1-eta(5)-C5H4-closo-1,2,3,4-C3B7H9)Fe (
4 )(1-) rings are linked to make a new type of ansa-allyl-cyclopentadienyl dianion that binds as a pent
6 water-catalyzed proton-transfer properties, AnsA and AnsB are shown to have drastically different lo
9 uctural homology isozymes L-asparaginases I (AnsA) and II (AnsB), which are shown via fluorescence sp
10 (CH(2))(3)NPh]Cl(2)(THF)(2) (5) with lithium ansa-bis-indenyl reagents Li(2)[XBI](Et(2)O) (XBI = (1-i
12 age achieved by MeLi, Bu(n)Li, and PhLi, the ansa bridge of [Me(2)Si(Cp(Me(2)))(2)]W(H)Cl is inert to
13 awing effect observed for a single [Me(2)Si] ansa bridge, a pair of vicinal [Me(2)Si] ansa bridges ex
14 m C-Si cleavage and functionalization of the ansa bridge, namely (Cp(Me(2)))(eta(5),kappa(1)-C(5)H(2)
18 The electronic influence of unbridged and ansa-bridged ring substituents on a zirconocene center h
19 Si] ansa bridge, a pair of vicinal [Me(2)Si] ansa bridges exerts an electron-donating effect relative
21 ron-donating effect of two vicinal [Me(2)Si] ansa bridges, relative to that of a single bridge, is a
22 drawing effect of the [Me(2)C] and [Me(2)Si] ansa-bridges is due to stabilization of the cyclopentadi
25 tion of 2 with FeCl2 produced three isomeric ansa-(CH2)2-ferrabistricarbadecaboranyl sandwich complex
26 re where the ring and cage are linked by the ansa -CH2CH2- group with attachment to the cage at the C
27 ricarbadecaboranyl ligands are linked by the ansa-CH2CH2- group at the C2 and C2' cage carbons, where
29 imilarities between the saliniketals and the ansa chain of the potent rifamycin antibiotics, which co
31 of the N2 carboxylation is controlled by the ansa-cyclopentadienyl ligand where the sterically demand
32 , strong intrinsic quenching of Nile red and ANSA dye fluorescence is observed on binding to a cytoch
33 gation and X-ray crystallography reveal that AnsA forms a tetrameric structure as a dimer of two inti
34 ) with a hypothetical 15.5kDa protein in the ANSA-GAP intergenic region (yeaA) of Escherichia coli, a
39 Kinetic analysis of the enzyme reveals that AnsA is positively cooperative, displaying a sigmoidal s
43 g that the so-called anterior nucleus of the ansa lenticularis (ALa) is the avian homolog of mammalia
44 egmenti, whereas the anterior nucleus of the ansa lenticularis in the avian diencephalon was renamed
45 ry, do not course ventromedially to form the ansa lenticularis, but rather, travel predominately medi
47 in the presence of enantiopure C1-symmetric ansa metallocene, {1,2-(SiMe2)2(eta5-C5H-3,5-(CHMe2)2)(e
48 e (5) and a method for its conversion to the ansa-metallocene [ethylene(eta5-inden-1-yl)(eta5-inden-2
49 ts, and ligand substitution pattern-cationic ansa-metallocene ester enolate catalyst 6(+)[B(C(6)F(5))
51 yclopentadienyl ligands together in strained ansa metallocenes are rare and limited to carbon-carbon
52 overall reductive elimination of RH from the ansa-molybdenocene and -tungstenocene complexes [Me(2)Si
56 , depending upon the linking position of the ansa-tether, constraints in cage-orientation, such as ob
57 The key step in the synthesis of the title ansa-titanocene (4) features a previously unreported equ
60 )(2)]WCl(2) provides a means to access other ansa tungstenocene compounds, such as [Me(2)Si(Cp(Me(2))
64 Treatment with excess Me3SiI furnished the ansa-zirconocene diiodide along with the N,N'-dicarboxyl
65 Addition of 2 equiv of carbon dioxide to the ansa-zirconocene dinitrogen complex resulted in selectiv
66 ction cleanly produces the isolable cationic ansa-zirconocene ester enolate complex rac-(EBI)Zr(+)(TH
67 aracterization, and abstraction chemistry of ansa-zirconocene ester enolate complexes relevant to the
68 ate in toluene produce the first examples of ansa-zirconocene mono- and diester enolate complexes: ra
69 of polar divinyl monomers, enabled by chiral ansa-zirconocenium catalysts through an enantiomorphic-s
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