ライフサイエンスコーパス: heterocyclic compound

1 ccess to a variety of underexplored strained heterocyclic compounds.

2 ds (PAs) comprising more than 350 individual heterocyclic compounds.

3 efficient synthesis of various five-membered heterocyclic compounds.

4 precursors for polyfunctionalized bioactive heterocyclic compounds.

5 easy access and a novel acylation method of heterocyclic compounds.

6 opentyne, as a tool for the synthesis of new heterocyclic compounds.

7 hly valued (fluorinated) nitrogen-containing heterocyclic compounds.

8 g to the observed affinity differences for N-heterocyclic compounds.

9 oxygen- and nitrogen-containing vicinal bis-heterocyclic compounds.

10 rting materials into an interesting class of heterocyclic compounds.

11 s for the synthesis of biologically relevant heterocyclic compounds.

12 synthesis of five-, six-, and seven-membered heterocyclic compounds.

13 n step in the thermal decomposition of these heterocyclic compounds.

14 etones and highly enantioenriched carbo- and heterocyclic compounds.

15 ead to highly functionalized carbocyclic and heterocyclic compounds.

16 e seen wide application for the synthesis of heterocyclic compounds.

17 ed 223 flavonoid, quinolizinium, and related heterocyclic compounds.

18 time produces a unique phosphorus-containing heterocyclic compound (20).

19 zo dimer tautomerizes and rearranges to form heterocyclic compound 3.

20 erved the formation of a hitherto unknown BN-heterocyclic compound 9 fused with a perimidine skeleton

21 A plethora of heterocyclic compounds are accessible by employing gamma

22 Nitrogen-containing heterocyclic compounds are an important class of molecul

23 lti-component reactions and the synthesis of heterocyclic compounds are discussed including the use o

24 Because heterocyclic compounds are routinely used in the promoti

25 , through a limited screen of selected small heterocyclic compounds, as a specific and high-affinity

26 d the cytotoxicity of AZB002 and the related heterocyclic compounds AZB004 and AZB016 and find that o

27 thod enables one-step preparation of complex heterocyclic compounds by alpha-alkenylation of readily

28 ntheses of members of several representative heterocyclic compound classes, including beta-lactams, 4

29 Likewise, when trichloromethyl heterocyclic compounds contain another reactive function

30 efficiently transformed into a rare class of heterocyclic compounds-dibenzo[b,f][1,5]diazocines-by a

31 s were tentatively identified as nitrogenous heterocyclic compounds (e.g., 3-chloro-5-hydroxy-1H-pyrr

32 yclopentadiene (Cp, 2) and the five-membered heterocyclic compounds (FHCs) furan 3 and N-methyl pyrro

33 [reaction: see text] We have designed two heterocyclic compounds for the colorimetric detection of

34 Piperidine is a 1-ring heterocyclic compound formed from the polyamine cadaveri

35 se products were structurally similar to the heterocyclic compounds formed during chlorination, such

36 We have synthesized novel heterocyclic compounds from resin-bound guanidines.

37 rialkylamine bases in the formation of these heterocyclic compounds has been established.

38 aromatic substitution reactions on different heterocyclic compounds has been examined.

39 pyrrole 4 for the construction of polycyclic heterocyclic compounds have been studied at the B3LYP/6-

40 Nitrogen-rich heterocyclic compounds have had a profound effect on hum

41 With the increased use of heterocyclic compounds in drug design, a rapid and effic

42 asily prepare a diverse array of substituted heterocyclic compounds in good yield.

43 f the tautomeric equilibria of pi-conjugated heterocyclic compounds in protic solvents and other H-bo

44 I) values of 192 nM to 84 muM), whereas some heterocyclic compounds inhibited the enzyme with K(I) va

45 hat the formation of halogenated nitrogenous heterocyclic compounds is reported from chloramination p

46 ctive synthesis of 5-5, 6-5, and 7-5 fused O-heterocyclic compounds is reported.

47 Indolizidines are bioactive heterocyclic compounds of great potential normally prepa

48 The reaction is useful for the generation of heterocyclic compounds of significant molecular complexi

49 me) by analysing the non-volatile oxygenated heterocyclic compounds (OHC) by UHPLC/TOF-HRMS, multivar

50 tals (Al, Fe, Cr, V) on the affinity for the heterocyclic compounds, on the integral adsorption entha

51 eterocycles during the synthesis of targeted heterocyclic compounds require the use of SF5 -functiona

52 e topoisomerase I (Top1) can be inhibited by heterocyclic compounds such as indolocarbazoles and inde

53 the transformations of propargylamines into heterocyclic compounds such as pyrroles, pyridines, thia

54 With the heterocyclic compounds, test calculations indicated the

55 les is to design GC binding selectivity into heterocyclic compounds that can get into cells and exert

56 (BTZs) are a new class of sulfur containing heterocyclic compounds that target DprE1, an oxidoreduct

57 rs allows a variety of functional groups and heterocyclic compounds to be tolerated.

58 The synthesis of these N-glycosylated heterocyclic compounds using traditional glycosylation m

59 ino acids, organic acids, carbohydrates, and heterocyclic compounds, using a simple and highly reprod

60 l calculations were performed on a series of heterocyclic compounds where the products resulting from

61 Urazole is a five-membered heterocyclic compound which is isosteric with uracil's h

62 This method allows synthesizing a variety of heterocyclic compounds, which are difficult to access fr

63 a buried cavity into which a number of small heterocyclic compounds will bind, providing a specific s

64 The synthesis of new chiral heterocyclic compounds with adjacent chiral centers is a

65 thalazin-1(2H)-ones (APOs) are underexplored heterocyclic compounds with promising and diverse biolog

66 strategy for rapid entry into triazole-fused heterocyclic compounds without recourse to the tradition