ライフサイエンスコーパス: functional group

1 , molecular weight, type and number of amine functional groups).

2 g that relate to geographic origin and plant functional group.

3 moreover depends on the positioning of this functional group.

4 to activate C-H bonds that are distal from a functional group.

5 ted dichloromethyllithium to Weinreb's amide functional group.

6 vative strategies for installing this unique functional group.

7 n previously reported ordered gradients in C functional groups.

8 developed methodology tolerates a variety of functional groups.

9 t role in particular for nitrogen containing functional groups.

10 to be mild and were amenable to a variety of functional groups.

11 operties of squaramides in contrast to other functional groups.

12 amides, and aryl rings having common organic functional groups.

13 ere more sensitive to antibiotics than other functional groups.

14 enzyl alcohols and tolerate a broad range of functional groups.

15 ith several compounds containing two organic functional groups.

16 efficient and the scope covers a variety of functional groups.

17 ster was demonstrated by conversion to other functional groups.

18 urred in the presence of other more reactive functional groups.

19 during VBNC induction than those lacking QS functional groups.

20 s for the predictable spatial arrangement of functional groups.

21 ofiber as there were no interactions between functional groups.

22 broad substrate scope and good tolerance of functional groups.

23 s that vary in size and that bear a range of functional groups.

24 ntroduction of a variety of P-loop-targeting functional groups.

25 n the abundance and community composition of functional groups.

26 fully covered by long-range ordered organic functional groups.

27 oisosteric replacements of ureas and related functional groups.

28 he full range of electrophilicity of organic functional groups.

29 nd without perturbing the hydration of these functional groups.

30 with tolerance for a range of base-sensitive functional groups.

31 tional group or those pollinated by multiple functional groups.

32 , contain the same distribution of IR-active functional groups.

33 o a low to no sorption tendency to organic C functional groups.

34 ificantly larger than each of its individual functional groups.

35 reaction conditions and tolerate an array of functional groups.

36 s spanning a range of chemical scaffolds and functional groups.

37 of substrates with reactive, acid-sensitive functional groups.

38 ese images were identified to density per 13 functional groups.

39 hose bearing base- and nucleophile-sensitive functional groups.

40 composed of multiple vegetation species and functional groups?

41 nsiders different numbers of species (1-60), functional groups (1-4) as well as functional identity (

42 Differences across functional groups (algae vs. corals) were apparent for t

43 sed analogues, using NH-Ts as a nucleophilic functional group allowed obtaining 10-membered azaenediy

44 between a target C-H bond and a coordinating functional group, along with the geometry of the cyclic

45 obtained for PFBS, which possesses the same functional group and a smaller molecular size compared t

46 enarios comprised of native individual plant functional groups and a coexisting multi-group compositi

47 rom a database on the basis of the number of functional groups and analysis of isotope labels distrib

48 rm the surface morphology, oxidation states, functional groups and charge transfer property of POC/MW

49 ive coupling is tolerant of a broad range of functional groups and demonstrates little sensitivity to

50 A promising approach to enumerate functional groups and elucidate molecular structures wit

51 study chemical structures of closely related functional groups and for the discovery of novel organic

52 The methodology tolerates a variety of functional groups and furnishes the desired products in

53 The reaction tolerated a wide range of functional groups and heteroaromatic moieties.

54 In some cases, adding polar functional groups and heteroatoms to the spiroadamantane

55 eductive defluorination tolerates a range of functional groups and heterocycles commonly found in bio

56 tment removes impurities, alters the surface functional groups and improves specific surface areas an

57 cy, resulting in the coexistence of multiple functional groups and performing the maximum amount of w

58 indoloquinoline precursors bearing versatile functional groups and provides a new approach for the sy

59 r vapour and oxygen transfer rate, textural, functional groups and secondary structure, thermal, crys

60 on of small molecules with a wide variety of functional groups and structural motifs.

61 elation between peak wavenumbers of specific functional groups and the amount of aggregate present.

62 the electron-donating ability of the organic functional groups and the electronegativity of the metal

63 This protocol tolerates a great variety of functional groups and thus provides a simple and step-ef

64 m mechanisms in humans can be broken down by functional groups and translated to model organisms.

65 Introducing suitable functional groups and/or counterparts in the hybrid stru

66 bstrates including those with base sensitive functional groups and/or multiple enolizable carbonyl gr

67 These drugs all feature N-methylamine functional groups, and certain N-alkylamines have been s

68 hydrocarbons, formation of oxygen-containing functional groups, and enhancement of OP(DTT) values.

69 s at low catalyst loading, tolerates several functional groups, and generates H(2)O as the sole bypro

70 e heterogeneity in size, the multiplicity of functional groups, and the highly convoluted charge-dist

71 ompounds bear a high density of redox-active functional groups, and their adsorption leads to a deple

72 ipped with a strategically substituted azide functional group are readily derivatized to the correspo

73 ine oxides and related phosphorus-containing functional groups are reported and compared to more comm

74 ractive surface patches acting as analogs of functional groups are used to assemble colloidal molecul

75 ine oxides and related phosphorus-containing functional groups are valuable polar structural elements

76 Plankton lifeforms (broad functional groups) are sensitive indicators of marine en

77 in sites and the designation of the aldehyde functional group as a structural alert by the medicinal

78 lecules by the introduction of similar bulky functional groups at their periphery.

79 conversion of carboxylic acid derivatives to functional groups bearing stereogenic centers via cascad

80 is ligand is displayed across a selection of functional groups, both under traditional borylation con

81 geometry, metal nodes, organic linkers, and functional groups, but at present we do not have a forma

82 c species with nonpolar and moderately polar functional groups, but lower recoveries were obtained fo

83 Overall, we have demonstrated that combining functional groups can enable the tuning of explosive and

84 rate the cell wall as well as chemicals with functional groups capable of interacting with wood polym

85 trostatic fields arising from remote charged functional groups (CFGs) can selectively and cooperative

86 ced through the use of nonconjugated charged functional groups (CFGs).

87 ork demonstrate the importance of atomic and functional group characteristics towards diversity of at

88 lementary ion pairs leading to more complete functional group characterization compared to CAD.

89 implications for the development of organic functional group chemistry.

90 1.30 +/- 0.16; p < 0.001) were higher in the functional group compared with the structural CMD and re

91 The exceptional functional group compatibility and site selectivity of C

92 of other reported protocols, exhibits a high functional group compatibility with mild conditions, and

93 Empowered with better functional group compatibility, novel derivatization str

94 ully prepared with good yields and excellent functional group compatibility.

95 h a reduced excess of substrate and improved functional group compatibility.

96 ained in high diastereoselectivity with good functional group compatibility.

97 perature, mild reaction conditions and broad functional group compatibility.

98 e starting materials, and it shows excellent functional group compatibility.

99 reaction proceeds efficiently with excellent functional group compatibility.

100 oceeds with a broad substrate scope and good functional group compatibility.

101 orides at an early and late stage with broad functional group compatibility.

102 The reaction shows excellent functional-group compatibility and is demonstrated to wo

103 Its wide functional-group compatibility is highlighted in the pal

104 The new method exhibits broad functional-group compatibility, operates under transitio

105 st evidence of clustering belong to just two functional groups: Components of immune response and met

106 clear whether alterations in GMB and related functional groups contribute to disrupted host metabolit

107 nopores), architecture (branched vs linear), functional groups (coordinating or ionic), specific prop

108 nctionalization reactions directed by innate functional groups could provide new routes to introduce

109 of products was obtained by controlling the functional groups directly bonded to the nitrogen atom o

110 The vast molecular heterogeneity and the functional group diversity of this complex mixture preve

111 hyl group (CF(2) D) represents a challenging functional group due to difficult deuterium incorporatio

112 The reaction is tolerant to a wide range of functional groups (e.g., halogen, nitrile, formyl, acety

113 raction, confinement, spillover, and surface functional group effects).

114 ional forces away from a mechanically active functional group embedded in one of its rings.

115 onyl scaffold allows facile variation of the functional groups, enabling labeling kinetics and select

116 a fixed direction, while the DNA serves as a functional group equivalent, connecting complementary br

117 tates the ion accessibility of these surface functional groups even at high current densities and lar

118 actions between bacteria and ionic electrode functional groups facilitated bacteria attachment at the

119 nonspecific fragmentation of all precursors, functional group families of precursors and product ions

120 As research on the structural and functional group features of FNAs and nanomaterials rapi

121 The concept of functional groups (FGs), sets of connected atoms that ca

122 layer of graphene oxide in order to provide functional groups for the covalent immobilization of the

123 dification also opens the door for attaching functional groups for various applications.

124 Difluorobenzodioxole is an important functional group found in both pharmaceuticals and agroc

125 The sulfone functional group has a strong capacity to direct the asy

126 g properties of sulfoximines, this versatile functional group has advanced to implementation in sever

127 ferences between C-H bonds located distal to functional groups has prevented the development of site-

128 Furthermore, species with similar functional groups have almost identical electrochemical

129 y investigated, comprehensive analyses of R-/functional groups have thus far been rare in medicinal c

130 and hydrophobic cavities, as well as exposed functional groups) have led to a tremendous increase in

131 into amine, triazole, tetrazole, and pyrrole functional groups highlight the broad utility of this me

132 orous silica material) modified with diverse functional groups (i.e. amine, carboxylic acid, isocyana

133 stematic variations in steric parameters and functional group identities established key structure-re

134 logy states that the electronic effects of a functional group in a molecule are possibly transmitted

135 imitations of this interesting and versatile functional group in medicinal chemistry and drug discove

136 stosoma mansoni by incorporating a weak base functional group in these compounds.

137 tants for Hg(II) complexes formed with thiol functional groups in bacterial cell membranes of two ext

138 omplex, highlighting the effect of substrate functional groups in influencing the protonation states

139 They are key functional groups in many pharmaceuticals, agro chemical

140 Aryl halides are ubiquitous functional groups in organic chemistry, yet despite thei

141 aturally present and artificially introduced functional groups in peptides including S-protected thio

142 The role of oxygen-containing functional groups in regulating the efficacy of CNT-enab

143 and Raman, have great potential for probing functional groups in single particles at ambient pressur

144 hat grazing reduced the correlations between functional groups in soil micro-food webs and then weake

145 stematic manner to identify fentanyl-related functional groups in such compounds based on their obser

146 ing effects, however, differed greatly among functional groups in the soil micro-food webs.

147 ersatile chemical transformations of surface functional groups in two-dimensional transition-metal ca

148 on, which can easily be converted to several functional groups including terminal alkyne, heterocycle

149 yl moiety to tether a plethora of productive functional groups, including reactive handles, purificat

150 Gylation and ligand conjugation) via various functional groups incorporated into the silica component

151 The peak absorbance of the OH functional group increased while the tryptophan contents

152 ity structure and productivity of a critical functional group, independent of live coral loss.

153 ves the selective modification of particular functional groups, inserting nuclei to act as reporters

154 e carried out in high yield (90%) with their functional groups intact.

155 Modest functional group interactions can play important roles i

156 ilization and characterization of other weak functional group interactions.

157 d the stereoselective assembly and selective functional group interconversions to access the structur

158 reover, by introducing isotopically enriched functional groups into the reagent structure, labeling s

159 Various functional groups involved in bacterial Zn binding were

160 This conversion and the functional groups involved in this conversion, until now

161 The late-stage introduction of this functional group is challenged by typical fluorination c

162 Importantly, the diazo functional group is retained within the molecule for fut

163 the alkB binding pocket to protect internal functional groups is also demonstrated.

164 Pd clusters and the nearby oxygen-containing functional groups is key for the high selectivity and ac

165 method tolerates a remarkably wide range of functional groups, is operationally simple, scalable, an

166 which refers to the number and type of plant functional groups, is the result of self-organization, o

167 nal olefins and tolerates a diverse array of functional groups (ketone, ester, amide, diketones, keto

168 trate that phosphine oxides are highly polar functional groups leading to high solubility and metabol

169 Mixing explosive functional groups led to changes in the explosive sensit

170 Functional group manipulations, including benzylic oxida

171 ne groups, suggesting permanganate access to functional groups may be important.

172 Our results explain how affinity-reducing functional groups may lead to affinity gains if combined

173 n, which includes the selection of polymers, functional group modifications, photoinitiators, and lig

174 i methodology, allowing for the inclusion of functional groups not otherwise accessible with current

175 osteric replacements of several heteroatomic functional groups, notably ureas, thioureas, guanidines,

176 lti-group composition scenario including all functional groups observed at the site are compared.

177 at the bacterivorous consumers, an important functional group of protists, were more sensitive to ant

178 that Ru(II) has intermolecular bonding with functional groups of GO.

179 aking alkaline pH value, coordinate with the functional groups of HD, and kill cancer cells by pro-ox

180 e) and the coordination between selenium and functional groups of HD.

181 ethod tolerates all other known nucleophilic functional groups of naturally occurring proteinogenic a

182 sitively co-varying and synchronously active functional groups of neurons.

183 ons and linking pesticide-induced changes in functional groups of organisms to ecosystem functions, t

184 eraction of trans-cinnamaldehyde modified CO functional groups of PLA and PBAT.

185 t pH 7.4 and 37 degrees C, and the effect of functional groups of polyphenols on MGO trapping ability

186 ootprinting is slow irreversible labeling of functional groups on amino acid side chains by targeted

187 A range of functional groups on aryl bromides as well as on heteroa

188 The reaction is successful with several functional groups on both the arene and the olefin inclu

189 structure that ensures excellent coverage of functional groups on carbon surface and facilitates the

190 fter HNO(3) treatment, the content of oxygen functional groups on HNO(3)-treated ACFC increased, whic

191 a linear product, and tolerates a variety of functional groups on quinoline and olefin moieties.

192 opy revealed a presence of oxygen-containing functional groups on the DLC surface.

193 cribe the specific role of oxygen-containing functional groups on the important environmental behavio

194 nfavorable interactions between KGlu and the functional groups on the protein surface, which drive bi

195 The functional groups on the pyrroles permit easy transforma

196 films with similar main chains but different functional groups on the side chain are employed to clar

197 s by deliberately grafting oxygen-containing functional groups onto CNT surfaces.

198 r plants pollinated exclusively by a non-bee functional group or those pollinated by multiple functio

199 However, the identification of functional groups or reagents that are mutually reactive

200 areas where they had to be amalgamated with functional group oriented synthetic planning considerati

201 with the absence of any traditional reactive functional groups other than a single alkene, render it

202 wever, the installation of multiple reactive functional groups (pai-bonds, leaving group, etc.) is re

203 The amide functional group plays a key role in the composition of

204 rix dependent inherent to the high number of functional groups present in carbohydrates.

205 Other functional groups present in the polymer bead play an im

206 with the vibrational modes of the phosphate functional group produced efficient absorption and high

207 The -NCS functional groups provide reactive handles for postsynth

208 aliphatic substituents and a broad range of functional groups, providing a variety of N-H pyrroles i

209 d is also compatible with a large variety of functional groups, providing good to excellent yields in

210 esis of illudinine is the use of the nitrile functional group, rather than an ester, as the functiona

211 the guests permits deciphering the effect of functional group replacements on Gibbs binding energies

212 AuNPs on GO surface due to masking of oxygen functional groups responsible for emission.

213 chosen based on comparable structure(s) and functional group(s).

214 strate precise molecular-weight control, CTA functional group scope, and accessible polymer architect

215 of its surface and the formation of surface functional groups (SFGs).

216 versity (hundreds of species) with only five functional groups spanning two essential trade-offs-the

217 A diverse array of functional groups such as esters, nitriles, alcohols, an

218 ine oxides and related phosphorus-containing functional groups such as phosphonates and phosphinates

219 exhibiting a single double bond as the only functional group, such as alpha-pinene, beta-pinene and

220 unctionalization of NHC surfaces with protic functional groups, such as alcohols and amines, particul

221 Polysaccharides possessing charged functional groups, such as chitosan, are known for mucoa

222 Such a sulfonyl group dance (functional group swap) results from a cascade of S(N)Ar

223 In addition, functional groups that are able to participate, such as

224 ra of common organic molecules which contain functional groups that are constituents of fentanyl is d

225 primary alkyl radicals and those containing functional groups that are susceptible to nucleophilic s

226 6) and partner crosslinking(7), the range of functional groups that can be introduced remains limited

227 Since C7 is spatially far away from any functional groups that could direct C-H activation, thes

228 ogonality between the azide and the hydroxyl functional groups, the former was next selectively react

229 By adjusting the molar ratio of crosslinking functional groups, the tensile strength was controlled,

230 While ketones are among the most versatile functional groups, their synthesis remains reliant upon

231 the face of climate change, the species and functional groups they benefit will be substantially alt

232 mployed to clarify the contributions of each functional group to contact electrification (CE).

233 ional reagents, enabling otherwise difficult functional groups to be appended to the carbene.

234 :1 interactions of crown ethers with various functional groups to be characterized in solution and th

235 all, the study presents a way to get distant functional groups to communicate with each other in a re

236 be incorporated by conjugating organic acid functional groups to graphite edges though aromatic phen

237 underlie different responses of species and functional groups to selective logging.

238 PTMs involve the covalent attachment of functional groups to specific amino acids.

239 cloisomerization, in the presence of all the functional groups, to give polyoxidized terpenes.

240 ic fluorinated and hydrophilic sulfonic acid functional groups, to produce membranes with negatively

241 many other ways to connect these two common functional groups together.

242 tion features mild reaction conditions, good functional group tolerability, and scalability.

243 trate scope (primary and secondary alcohols) functional group tolerance (amino, nitro, halo, alkoxy,

244 ssociation energy as well as a wide range of functional group tolerance (e.g., ethers, halides, thioe

245 oichiometric ratio of reactants and has high functional group tolerance (phenols, amides, ethers, car

246 Pd-BNP showing a wide range of functional group tolerance and an immense array of subst

247 Remarkable functional group tolerance has also been demonstrated.

248 tion/gem-diborylation of alkynes with a high functional group tolerance is presented.

249 The exceptional functional group tolerance observed under the optimized

250 h that is based on the excellent control and functional group tolerance of ring-opening metathesis po

251 The broad generality and functional group tolerance of this method is extensively

252 d featuring a broad substrate scope and high functional group tolerance remains elusive.

253 The Pd-BNP catalyst showed a wide range of functional group tolerance that enabled building a libra

254 In addition, a very good functional group tolerance was observed in these reactio

255 A wide substrate scope and high functional group tolerance were observed in both approac

256 of this method include the following: broad functional group tolerance, a biorenewable methine sourc

257 od features a broad substrate scope and good functional group tolerance, and the in situ-generated HC

258 The reaction exhibits excellent functional group tolerance, as demonstrated by the boryl

259 alpha,E- or beta,E-selectivities and a broad functional group tolerance.

260 oward pyrrolocarbazoles with broad scope and functional group tolerance.

261 aration of KATs in high yields and with good functional group tolerance.

262 lines in good to excellent yields, with high functional group tolerance.

263 bonds in bromoiodoarenes and exhibits broad functional group tolerance.

264 lds of the N-heterocycle products with broad functional group tolerance.

265 es and 1,5-enynes with good atom economy and functional group tolerance.

266 ally to imines in 30-91% yields, with a good functional group tolerance.

267 oxygen, sulfur and nitrogen atoms with broad functional group tolerance.

268 s, display a broad scope, and show excellent functional group tolerance.

269 alyst or additives required and display good functional group tolerance.

270 cted efficiently with a broad scope and high functional group tolerance.

271 source in moderate to good yields, with good functional group tolerance.

272 ization showed wide substrate scope and good functional group tolerance.

273 thereby demonstrating its broad utility and functional group tolerance.

274 The reaction shows outstanding functional-group tolerance with respect to both the alph

275 With good functional-group tolerance, alkyl and benzyl amine deriv

276 n exhibits a broad substrate scope, has high functional-group tolerance, and can be employed for the

277 od exhibits a broad substrate scope and high functional-group tolerance, and it accommodates a divers

278 er, which renders complexes of titanium less functional group tolerant than their late transition met

279 Functional-group-tolerant Lewis acid catalysts are there

280 hemoselective C-H hydroxylation with a mild, functional-group-tolerant methylation.

281 the broad synthetic potential of this highly functional-group-tolerant reaction.

282 ability to inactivate toxic and chromophore functional groups, transform impurities into an easily r

283 ly, our group reported that enone and ketone functional groups, upon photoexcitation, can direct site

284 127 VOCs were classified based on the functional group using the spectral and structural netwo

285 M Au chips followed by in situ activation of functional groups using EDC-NHS crosslinkers, grafting o

286 h common fragments/core structure and mutual functional groups, using precursor lines and neutral los

287 Adequate tolerance of valuable functional groups was also observed, such as olefins pos

288 Compatibility with common organic functional groups was observed with the reduced cobalt(0

289 tions directed by weakly coordinating native functional groups was unreported.

290 Bpin)(2), tolerates nitro, halide, and amino functional groups well, and this amide reduction is comp

291 transcription levels of genes from the same functional group were affected by the absence of PARP-1

292 riety of arylacetonitriles bearing different functional groups were converted into the corresponding

293 tructure of silk fibroin (possessing lots of functional groups which are suitable for attachment of l

294 relative proximity and orientation of common functional groups, which can influence a chemical exchan

295 etition, promoting coexistence between plant functional groups, which ultimately mitigates the impact

296 to mimic biological functions of traditional functional groups while providing a wide variety of phar

297 c tables of such transformations, divided by functional groups, will be provided, thus enabling a use

298 different ketones bearing a wide variety of functional groups with an average yield of 60+/-16 %.

299 ncluding building blocks, reactive sites and functional groups with the aim of finding the origins of

300 he precise placement of multiple cooperative functional groups within a framework, leading to emergen