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1 ing two A-type linkages (C4-->C8 and C7-O-C2 ether linkages).
2 e of the substituent or replacing it with an ether linkage.
3 t example representing the dominant beta-O-4 ether linkage.
4 cally challenging chiral tertiary alkyl-aryl ether linkage.
5 ompound containing a highly twisted diphenyl ether linkage.
6 ontains a stereogenic axis across the diaryl ether linkage.
7 stituted onto cyclooctatetraene (COT) via an ether linkage.
8 ent addition of palmitic acid through a thio-ether linkage.
9 , particularly when their ligands contain an ether linkage.
10  ethers with complexity on both sides of the ether linkage.
11 henols upon irradiation via photocleavage of ether linkages.
12 ch the amide functionalities are replaced by ether linkages.
13 the Ru(IV) allyl to generate trans-2-butenyl ether linkages.
14 nding polycarbonate with a minimal amount of ether linkages.
15 s decomposed at slower rates than those with ether linkages.
16 zene and catechol building units, which form ether linkages.
17 n centers including a chlorinated carbon and ether linkages.
18 ymeric backbone: either direct (1) or via an ether linkage (2).
19 lish the stereogenic centers adjacent to the ether linkage and a ring-closing metathesis reaction to
20 phospholipid vesicles containing sn-1 and -2 ether linkages and sphingomyelin at Ca2+ concentrations
21 he N-terminal nucleophile of ThnT through an ether linkage, and analysis suggests inactivation throug
22                      Here we introduce silyl ether linkage as a novel dynamic covalent motif for dyna
23  alkylation to construct the tert-alkyl aryl ether linkage between the dopa and isoleucine residues.
24 ole ratios, lignin with controlled levels of ether linkage content, hydroxyl group content, and avera
25   Copolymers comprising ester, carbonate, or ether linkages could fulfill some of this demand as thei
26 reaction with them to produce monoalkylated (ether-linkaged) cyclodextrin derivatives are discussed a
27 oly(ester-alt-ethers) can combine beneficial ether linkage flexibility and polarity with ester linkag
28  the Z-val-cit-p-amidobenzyl alcohol through ether linkages, forming the peptide-drug derivatives 8 a
29 an be produced with up to 80% yield, whereas ether linkage-free lignin with low polydispersity can be
30                                     Although ether linkages have been hypothesized as potential react
31 ly construct an aromatic ring and the diaryl ether linkage in one step.
32                       The replacement of the ether linkage in triclosan by a carbon bridge in hexachl
33 formation caused by unimolecular cleavage of ether linkages in homooxacalix[3]arene ligands during gr
34 th the discovery of monomer-invariant aryl-O-ether linkages in lignins that upon alkaline cleavage re
35 henylboronic acids to 5-thymidine through an ether linkage installed using Mitsunobu conditions with
36 ne other occasion converted the benzhydryl O-ether linkage into an oxime-type derivative.
37                  By incorporating such silyl ether linkages into covalently cross-linked polymer netw
38              The relative dehydration of the ether linkage is consistent with it promoting more dense
39               The reductive cleavage of aryl ether linkages is a key step in the disassembly of ligni
40                      The substitution of the ether linkage of ABT-770 (5) with a sulfone group 13a le
41 -catalyzed oxidative hydrolysis of the vinyl ether linkage of arachidonoyl-plasmalogens.
42                                          The ether linkage of C4-C5 in the morphinan ring leads to a
43 ubstitution of oxygen for sulfur in the sn-1 ether linkage of ilmofosine.
44 the archaeal structural features typified by ether linkage of the glycerol backbone to isoprenoid cha
45            The cleavage of the beta-O-4 aryl ether linkages of lignin followed by extensive C-C conde
46 ha-keto and alpha-hydroxy beta-O-4 type aryl ether linkages of lignin.
47 set of three adjacent bromines, and a methyl ether linkage on the phenyl ring.
48  the R-configuration and the advantage of an ether linkage over an ester linkage.
49  pathway in order to cleave the racemic beta-ether linkages that are present in the backbone of the l
50 uring lignin biosynthesis, resulting in less ether linkages that generate monomers.
51 niform incorporation of acid-degradable enol ether linkages throughout the copolymers, which enables
52 seryl side chain attached through an unusual ether linkage to the core nocardicin framework.
53 e resulting chiral center, is attached by an ether linkage to the pro-S hydroxymethyl group (sn-1 pos
54 ng novel hybrid materials possess silyl aryl ether linkages to the silica surface that are thermally
55 eaction for formation of the required diaryl ether linkage was successfully tested on a model system.
56 roso acetal tosylate 17 containing the silyl ether linkage was thwarted by a slow alkylation and an u