ライフサイエンスコーパス: facile preparation of

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1 versatile 1,4-diketone surrogates, allowing facile preparation of 2,3,5-trisubstituted furans, pyrro

2 This result enables the facile preparation of a 64-residue peptide (alpha)thioes

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 A facile preparation of a high-load, soluble oligomeric al

6 A facile preparation of a mesoporous Cr-MOF, PCN-333(Cr) w

7 Facile preparation of a novel chiral 2-aminoDMAP core ca

8 This route allowed for the facile preparation of a number of analogs that were desi

9 -sulfinyl ligand class is highlighted by the facile preparation of a variety of sterically and electr

10 mon organic solvents enabling its use in the facile preparation of acid-sensitive microparticles.

11 hesis (RCM)/Kharasch addition allows for the facile preparation of bicyclic [3.3.0], [4.3.0], and [5.

12 ew route to organofluorides was used for the facile preparation of biomedically valuable compounds.

13 In this report, we demonstrate the facile preparation of diverse and functional nanoparticl

14 stitution reactions were employed toward the facile preparation of functional oligomers and macromole

15 The methodology permits the facile preparation of glycolipids which vary in the leng

16 ynthetic value of this building block in the facile preparation of GSH bioconjugates in a satisfying

17 We report on the facile preparation of highly scattering metal-coated pol

18 The facile preparation of highly sensitive electrochemical b

19 vity for benzylic oxidation, and enables the facile preparation of isotopically enriched 15N-labeled

20 orded by these qualities further allowed the facile preparation of macrocyclic sheet structures from

21 Finally, the facile preparation of mono- and disubstituted oxazoles f

22 We report the facile preparation of O2-sulfonated diazeniumdiolates an

23 rrent standard Michael reaction and used for facile preparation of organic compounds of widely differ

24 We report a new method for the facile preparation of plasmenylcholine via reaction of l

25 The facile preparation of (S)-N-tosylamidofuran 16 and its c

26 In this paper, a facile preparation of SF5-substituted pyrrole carboxylic

27 , this thermo-reversible behavior allows the facile preparation of sterile gels, since ultrafiltratio

28 in and E- and Z-pinnatifidenyne as well as a facile preparation of the oxocene core of 3E-dehydrobrom

29 The facile preparation of the salts, their ease of handling,

30 The facile preparation of this Co-S film, along with its low

31 Other advantages include more facile preparation of trace element stock solutions, a r

32 This simple, one-step procedure allows a facile preparation of unstable glycosylamines in contras

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