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1 versatile 1,4-diketone surrogates, allowing facile preparation of 2,3,5-trisubstituted furans, pyrro
3 des and a variety of electrophiles allow the facile preparation of a diverse array of annulation prod
4 In this paper, we demonstrate the rapid and facile preparation of a family of nanoparticles with dif
5 on of a bipyridyl ligand, we demonstrate the facile preparation of a heterogenized nickel electrocata
10 -sulfinyl ligand class is highlighted by the facile preparation of a variety of sterically and electr
11 mon organic solvents enabling its use in the facile preparation of acid-sensitive microparticles.
14 th ester groups could be achieved, providing facile preparation of an indolizidine framework commonly
15 h the rapid C-P bond-forming reaction allows facile preparation of aryl phosphorus target compounds f
16 from a synthetic pathway that allows for the facile preparation of asymmetric redox-active Au(I) bis-
17 hesis (RCM)/Kharasch addition allows for the facile preparation of bicyclic [3.3.0], [4.3.0], and [5.
18 ew route to organofluorides was used for the facile preparation of biomedically valuable compounds.
20 stitution reactions were employed toward the facile preparation of functional oligomers and macromole
22 ynthetic value of this building block in the facile preparation of GSH bioconjugates in a satisfying
25 vity for benzylic oxidation, and enables the facile preparation of isotopically enriched 15N-labeled
26 orded by these qualities further allowed the facile preparation of macrocyclic sheet structures from
29 rrent standard Michael reaction and used for facile preparation of organic compounds of widely differ
33 , this thermo-reversible behavior allows the facile preparation of sterile gels, since ultrafiltratio
34 ce and untangles fundamental mechanisms of a facile preparation of sulfur-containing, biorelevant org
35 in and E- and Z-pinnatifidenyne as well as a facile preparation of the oxocene core of 3E-dehydrobrom
40 This simple, one-step procedure allows a facile preparation of unstable glycosylamines in contras
41 tive cross-coupling approach allowed for the facile preparation of various C20-arylated derivatives t