ライフサイエンスコーパス: heterocyclic compound

1 hol, 5 acids, 11 aldehydes, 5 ketones and 16 heterocyclic compounds).

2 nditions for easy access of various arylated heterocyclic compounds.

3 her modified to generate difficult-to-access heterocyclic compounds.

4 clic hydrocarbons, nonbenzenoid systems, and heterocyclic compounds.

5 reductive dearomative functionalization for heterocyclic compounds.

6 oromethylation, etc., applied across various heterocyclic compounds.

7 or the preparation of highly enantioenriched heterocyclic compounds.

8 des, and a wide range of nitrogen-containing heterocyclic compounds.

9 ccess to a variety of underexplored strained heterocyclic compounds.

10 s for the synthesis of biologically relevant heterocyclic compounds.

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

12 efficient synthesis of various five-membered heterocyclic compounds.

13 precursors for polyfunctionalized bioactive heterocyclic compounds.

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

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

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

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

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

19 rting materials into an interesting class of heterocyclic compounds.

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

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

22 as ergot, hapalindole alkaloids, and related heterocyclic compounds.

23 etones and highly enantioenriched carbo- and heterocyclic compounds.

24 ead to highly functionalized carbocyclic and heterocyclic compounds.

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

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

27 for the oxygenation of a diverse range of N-heterocyclic compounds.

28 the efficient preparation of pyrazole-based heterocyclic compounds.

29 n of remote stereocenters and highly complex heterocyclic compounds.

30 of novel synthetic chiral oxygen-containing heterocyclic compounds.

31 mediates derived from conjugated alkenes and heterocyclic compounds.

32 range of 2-amidated indoles as well as other heterocyclic compounds.

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

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

35 -C bond activation to give the unusual spiro-heterocyclic compound (5).

36 The potentially toxic heterocyclic compound, 5-hydroxymethylfurfural (HMF) was

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

38 Furans, polyols, N-heterocyclic compounds, aldehydes, ketones, and esters a

39 bonyl compounds, polyhydroxyalkyl pyrazines, heterocyclic compound and alkylimidazoles.

40 her exploration of the products to construct heterocyclic compounds and other functionalities.

41 re an important class of biologically active heterocyclic compounds and potential drug candidates.

42 chemistry of (hetero)cycles, N-vinylation of heterocyclic compounds, and palladium-catalyzed cross-co

43 A plethora of heterocyclic compounds are accessible by employing gamma

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

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

46 Chiral oxygen-containing heterocyclic compounds are of great interest for the dev

47 Because heterocyclic compounds are routinely used in the promoti

48 duce synthetically and biologically valuable heterocyclic compounds are salient features of this nove

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

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

51 ort the first synthesis of a family of novel heterocyclic compounds based on a 5-dihydropyrazolo[3',4

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

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

54 Likewise, when trichloromethyl heterocyclic compounds contain another reactive function

55 ds to the generation of unique spiro-bridged heterocyclic compounds containing amide, indanone, and o

56 Skatole is a pungent heterocyclic compound derived from the essential amino a

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

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

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

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

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

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

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

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

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

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

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

68 satile and most utilized nitrogen-containing heterocyclic compounds in academia and industry.

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

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

71 cess to substituted five-membered carbo- and heterocyclic compounds in good yields and excellent enan

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

73 tions (MCRs) are commonly used to synthesize heterocyclic compounds including tetrahydro-4H-chromene

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

75 -light mediated aerobic dehydrogenation of N-heterocyclic compounds is a reaction with enormous poten

76 soquinolines for the construction of complex heterocyclic compounds is also demonstrated.

77 nally functionalized alkyl, carbocyclic, and heterocyclic compounds is described.

78 The synthesis of heterocyclic compounds is particularly important since t

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

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

81 Thus, we hypothesised that Se-containing heterocyclic compounds might curb the activity of SARS-C

82 Heterocyclic compounds of elements with double bonds are

83 Indolizidines are bioactive heterocyclic compounds of great potential normally prepa

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

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

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

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

88 ounds such as other cycloalkane derivatives, heterocyclic compounds, stereodefined 1,3-dienes, and li

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

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

91 dented opportunity for N-containing aromatic heterocyclic compounds synthesis from biorenewable feeds

92 With the heterocyclic compounds, test calculations indicated the

93 g nitrogen into sugars to produce valuable N-heterocyclic compounds that are amenable to further modi

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

95 Despite abundant emissions, heterocyclic compounds that included furans contribute t

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

97 tro, halo, alkoxy, thiomethoxy, and S- and N-heterocyclic compounds) that can be scaled up.

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

99 content of over 90% was unknown for a binary heterocyclic compound until now.

100 2-(Methylthio)-1,3-dithioles are important heterocyclic compounds used for the preparation of redox

101 This work reports the preparation of complex heterocyclic compounds using direct metalation of thioph

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

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

104 lycyclic aromatic hydrocarbons, and nitrogen-heterocyclic compounds were detected, which had properti

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

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

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

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

109 ine, is a large group of nitrogen-containing heterocyclic compound with diverse chemical structure an

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

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

112 t produce a range of functionalized aromatic heterocyclic compounds with pyrazole/pyrazoline cores ha

113 n important class of biologically privileged heterocyclic compounds with several key applications in

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