ライフサイエンスコーパス: starting material

1 ent DNA for sequencing from small amounts of starting material.

2 different products originating from the same starting material.

3 nitrophenyl trifluoromethanesulfonate as the starting material.

4 attractive, and thus favorable petrochemical starting material.

5 tners simultaneously, using small amounts of starting material.

6 ative increase of AX content compared to the starting material.

7 nsitivity, reduced analysis time, and minute starting material.

8 mercially available sugar derivatives as the starting material.

9 from the nano- to microscale, using a single starting material.

10 ding enantioenriched enaminone and recovered starting material.

11 en ultrasmall primary samples can be used as starting material.

12 m, using chemically expanded graphite as the starting material.

13 pplications that demand a large(r) amount of starting material.

14 DDGS is consistently uniform irrespective of starting material.

15 t time in only 18 steps from a simple olefin starting material.

16 which uses unfractionated human PBMCs as the starting material.

17 the biological space of the natural product starting material.

18 labor-intensive and require highly purified starting material.

19 hour, using an actively dividing culture as starting material.

20 trifugation steps and substantial amounts of starting material.

21 cts reflect the molecular composition of the starting material.

22 specialized expertise and a large amount of starting material.

23 )(CO)((t)BuPy)](+) ([1-MH](+)) from an Ir(I) starting material.

24 bove all, more unsaturated than the original starting material.

25 ultams in one step, using saccharin anion as starting material.

26 h concentration using commercially available starting materials.

27 if there is residue water remaining from the starting materials.

28 functionalized arenes from readily available starting materials.

29 ch to generate complex molecules from simple starting materials.

30 two steps from cheap, commercially available starting materials.

31 rks in six steps from commercially available starting materials.

32 tructures, metamaterials, and robots from 2D starting materials.

33 xidized thioimidates from readily accessible starting materials.

34 sive cyclopentadiene and diethyl fumarate as starting materials.

35 excellent yields from the readily available starting materials.

36 a bespoke sulfinylamine (R-N=S=O) reagent as starting materials.

37 om different low-cost and readily accessible starting materials.

38 ate complexity through elaboration of simple starting materials.

39 gical processes, from the simplest plausible starting materials.

40 ergent for pseudo-symmetric allylic chloride starting materials.

41 bisphenalenyls in <=7 steps from commercial starting materials.

42 ubstituted porphyrins from readily available starting materials.

43 s in three steps from commercially available starting materials.

44 ains reliant upon reactive and low-abundance starting materials.

45 access 1,4-dicarbonyl compounds via umpoled starting materials.

46 ic amines from simple commercially available starting materials.

47 thylidene)oxindoles and 1,4-benzoxazinone as starting materials.

48 l-myo-inositol, derived from the same set of starting materials.

49 omerization in cyclopentene and cycloheptene starting materials.

50 and organocatalysts, from readily available starting materials.

51 g furan and Cbz-protected glycol aldehyde as starting materials.

52 optimizations from comparatively inexpensive starting materials.

53 powders of tantalum or niobium (20 vol.%) as starting materials.

54 ated nucleobases or nucleobase precursors as starting materials.

55 able carbonyl compounds from easily accessed starting materials.

56 l-substituted chiral aziridines from achiral starting materials.

57 cope from abundant and complex aryl chloride starting materials.

58 requisite trifluoromethyl-substituted alkene starting materials.

59 col was generated in 4 steps from commercial starting materials.

60 er and readily available indole analogues as starting materials.

61 3 in seven steps from commercially available starting materials.

62 vailable amines, anilines, and bisphenols as starting materials.

63 nder mild conditions from readily accessible starting materials.

64 from inexpensive and commercially available starting materials.

65 ed in high yield from commercially available starting materials.

66 ry and quaternary centers from simple alkene starting materials.

67 e pi-systems might be accessible from simple starting materials.

68 onalized heterocycles from readily available starting materials.

69 les in two steps from commercially available starting materials.

70 arylhydrazines and o-alkynylbenzaldehydes as starting materials.

71 of quaternary centers from easily available starting materials.

72 red in multigram quantities from inexpensive starting materials.

73 the reaction and general availability of the starting materials.

74 creased gas uptake capacities as compared to starting materials.

75 t physical properties from readily available starting materials.

76 naturally occurring, and chemically diverse starting materials.

77 ires the availability and use of oxygen-free starting materials.

78 of alkenes and alkynes, including sensitive starting materials.

79 ng structurally complex products from simple starting materials.

80 ant on a limited pool of chiral carbohydrate starting materials.

81 hesis of benzoxazole derivatives using these starting materials.

82 by the extrusion of a carbonyl unit from the starting materials.

83 can be sustained by feeding the system with starting materials.

84 ms of accessibility and affordability of the starting materials.

85 resceins from readily available, inexpensive starting materials.

86 oducts and studies with isotopically labeled starting materials.

87 ss to three different products from the same starting materials.

88 ables oxidation states to be embedded in the starting materials.

89 t are less thermodynamically stable than the starting materials.

90 ing myo-inositol and ethyl propiolate as the starting materials.

91 ctants which can be prepared from wood-based starting materials according to the principles of xyloch

92 Using fluorinated starting materials, after mesylation, allowed for the de

93 ucted from two classes of commonly available starting materials, alkenes and carbon-hydrogen (C-H) bo

94 These reactions employ readily available starting materials (alkyl halides, alkenes, etc.) and si

95 ile methodology, involving readily available starting materials, allows for the synthesis of stable h

96 tide stereotriads from the same alpha-chiral starting material and avoids potentially epimerizable al

97 cid intermediate, derived from the arylamine starting material and CO2 in the presence of DBU, is deh

98 The route commences from a renewable furan starting material and features a number of unusual trans

99 mplex oligomeric catalysts both racemize the starting material and select one enantiomer for a highly

100 tive use of (-)-quinic acid as a chiral pool starting material and substrate stereocontrol to establi

101 bular level of dispersions, were used as the starting material and the 3D-NDP-ACMs were obtained via

102 valent library (DCL) consisting of the eight starting materials and 16 condensation products.

103 ional handling of toxic or pyrophoric P(III) starting materials and 2) a dependence on hazardous fluo

104 This method utilizes readily available starting materials and allows for the preparation of the

105 development, as such a method involves cheap starting materials and allows in situ generation of a re

106 iety can be generated from readily available starting materials and by the use of commercially availa

107 idly builds molecular complexity from simple starting materials and cannot be accomplished with high

108 Using simple starting materials and commercially accessible catalysts

109 fficiently assembled using readily available starting materials and conjugated to ASOs using a soluti

110 In this work, we utilized (15)N-labeled starting materials and continuous high-sensitivity (1)H-

111 utilizes easy-to-handle phosphine oxides as starting materials and effectively replaces harsh fluori

112 The ready availability of starting materials and key Wittig olefination, ring-clos

113 ach is to use ubiquitous carboxylic acids as starting materials and perform a decarboxylative couplin

114 elds, use of cost-effective and eco-friendly starting materials and photosensitizer, and energy effic

115 ntane ring from simple and easily accessible starting materials and rapidly installs the C1/C4/C5 pol

116 ts necessary for the adaptation to different starting materials and reagents while ensuring the same

117 ct shock recovery experiment to simulate the starting materials and shock conditions associated with

118 modular approach uses commercially available starting materials and simple chemical transformations.

119 a]quinoxalinones from commercially available starting materials and their use in preparing potential

120 d for synthesis of geometrically pure alkene starting materials and therefore constitutes a significa

121 lative to their constituent olefin and amine starting materials and thus are not accessible via direc

122 convenient exploitation of native IgG as the starting material, and a well-defined conjugation site f

123 there is a kinetic resolution of the racemic starting material, and its magnitude is correlated with

124 s easily scaled to use more than one gram of starting material, and the products can be readily diver

125 strategy used inexpensive levoglucosan as a starting material, and we achieved a microwave glycosyla

126 nthesis features applications of chiral pool starting materials, and catalyst-, substrate-, and auxil

127 ld reaction conditions and easily accessible starting materials, and it shows excellent functional gr

128 ved products do not account for all consumed starting materials, and mechanistic ambiguities remain.

129 rate scope, using easy-to-handle alcohols as starting materials, and performing the reactions under a

130 Easy operation, readily accessible starting materials, and short syntheses of the privilege

131 polymer conjugates are synthesized from pure starting materials, and the struggle to separate conjuga

132 e translation is active and large amounts of starting material are readily available.

133 and methods making use of biomass-accessible starting materials are also rare.

134 allic compound), and the available anhydrous starting materials are also surveyed.

135 The starting materials are easily prepared, and the use of w

136 is limited by the behaviour of common boron starting materials as archetypal Lewis acids such that c

137 ks is presented using inexpensive commercial starting materials as opposed to previous syntheses of t

138 y is driven by the broad availability of the starting materials as well as the kinetic and thermodyna

139 roups (67-84% yields from a common hydantoin starting material) as well as a spiroligomer trimer 25 w

140 ully on both cyclic and acyclic amino ketone starting materials, as well as a range of substituted gu

141 ated Z-products from easily accessible diene starting materials bearing a Z-olefin moiety.

142 overall synthetic approach stems from chiral starting material benzyl (S)-2-methyl-4-oxopiperidine-1-

143 ational predisposition of the anthranilamide starting material brings the aryl rings into proximity a

144 en centers, all used marrow aspirates as the starting material, but no two centers used the same manu

145 ents and reduced the antioxidant capacity of starting material by up to 94%.

146 easily prepared from commercially available starting materials by cross-coupling reactions, many des

147 synthetic methods that generate the required starting materials by forming the central C-C bond, it e

148 olving initial 2e(-) oxidation of the Ni(II) starting materials by the F(+) transfer reagent N-fluoro

149 pplied to any cell type, provided sufficient starting material can be collected.

150 organism, as long as a sufficient amount of starting material can be obtained.

151 eries of simple and unbiased aliphatic amine starting materials can be oxidized to value-added ketone

152 : having simple operation, easily accessible starting materials, chemoselective cascade process, synt

153 several characteristics in the polyphenolic starting material composition were tentatively suggested

154 torage, all six urine samples from different starting materials converged to these characteristics.

155 (99.9 LC area %) in 49.8% overall yield from starting material DLAC (1).

156 ehydration of aldoximes as readily available starting materials due to their easy preparation from al

157 re typically prepared from prefunctionalized starting materials, e.g. using the Sonogashira coupling,

158 eatures inexpensive and easily synthesizable starting materials, easy operations, and a high efficien

159 emplates as instructions to a mixture of all starting materials elicits system-level behavior.

160 ly accessible through commercially available starting materials, enables a modular approach for the s

161 ,3-disubstituted pyrroles from the available starting materials (enolizable ketones and acetylene).

162 action of insoluble-bound phenolics from the starting material (experiment I) or the residues contain

163 study them require a considerable amount of starting material, favor the recovery of only a subset o

164 ods to synthesize chiral allenes from chiral starting materials, fewer methods exist to directly synt

165 supported diborane(6) 2, which served as the starting material for all subsequent transformations.

166 ize various substituted pyrroles useful as a starting material for broad applications.

167 Molecular tools require DNA as the starting material for diagnosis, and hence, a prerequisi

168 Glucose, the starting material for glycolysis, is transported through

169 Chitin has become a valuable starting material for many biotechnological products thr

170 hen, a major egg industry byproduct, as the starting material for preparing antihypertensive peptide

171 term maintenance and efficient production of starting material for SSC culture.

172 ion of 1,6-diol was found to be a convenient starting material for the synthesis of aminocyclitols an

173 Acyl amidines in particular can be used as a starting material for the synthesis of heterocycles and

174 hey are found, this implies that some of the starting materials for life are likely to be widely dist

175 Dienes are ubiquitous and easily synthesized starting materials for organic synthesis, and alkyl acry

176 r nitrogen atom, allowing them to be used as starting materials for parallel library synthesis and as

177 ox-active esters were found to be convenient starting materials for simple, thermal, Ni-catalyzed rad

178 organic synthesis and have become invaluable starting materials for the construction of multifunction

179 ristics of compound fragments make them good starting materials for the development of compound libra

180 ped a synthetic route to mixed dianilides as starting materials for the N-N coupling.

181 principle represent attractive and abundant starting materials for the preparation of substituted cy

182 e employing cycloalkylamines as multifaceted starting materials for the synthesis of nylon building b

183 lanine or 4-iodobenzyl bromide served as the starting materials for the synthesis of three iodinated

184 urkish accessions might be most promising as starting materials for the tomato processing and breedin

185 Using readily available starting materials from chiral pool, a variety of carbon

186 The synthesis uses the widely available starting material guanosine via a short sequence ending

187 nnulation reaction of two readily accessible starting materials has been developed for building seven

188 Besides aldehydes, ketones, or amines, starting materials have been used that can be converted

189 reactions using the title compound as a key starting material, have been described in recent years.

190 This reaction features readily available starting materials, high atom economy, broad substrate s

191 -glycosides can be synthesized from the same starting material in nearly all cases examined.

192 oor functional groups from readily available starting materials in a more efficient manner.

193 ular structures is the utilization of common starting materials in chemodivergent transformations.

194 ess to a broad range of products from simple starting materials in good yields and up to >99% ee and

195 roup 14 elements are well-known as versatile starting materials in many chemical transformations, a h

196 The obtained products were used as starting materials in the preparation of novel fluorinat

197 ly available substituted phenols are used as starting materials in the reaction sequence composed of

198 ng thiols or disulfides, as widely available starting materials, in combination with KF, as an inexpe

199 sciences, which traditionally used cells as starting materials, in particular tissue engineering, re

200 from a single fractionation protocol (2g MD starting material), including solvent partitioning throu

201 ized in 6 to 10 steps from readily available starting materials, including (+)-corynoline, (+)-anhydr

202 eloped herein utilizes entirely bench stable starting materials, including organotrifluoroborates, en

203 tion strategy that employs readily available starting materials, inexpensive reagents, and convenient

204 ess accessible and unpleasant arenethiols as starting materials, instead utilizes very stable aryl ha

205 rearrangement, the THF bound to the neutral starting material is expelled, and the Fe-Fe distances w

206 implicity: no prefunctionalization of either starting material is required, the reaction is insensiti

207 about severe sample loss from low amount of starting material is widely presumed in the proteomics f

208 neration of molecular complexity from simple starting materials is a key challenge in synthesis.

209 oline-fused eight-membered rings from simple starting materials is described.

210 stituted glutarimides from readily available starting materials is developed using oxidative N-hetero

211 ions, a clean and complete conversion of the starting materials is observed and the dimeric products

212 ynthetic value from inexpensive and abundant starting materials is of great importance.

213 cal products and their synthesis from simple starting materials is of great interest.

214 analogues of olefins from readily available starting materials is reported.

215 Thorough mixing of the starting materials is the first step of a crystal growth

216 vantageously maintains the morphology of the starting material, is stable against reaggregation and c

217 onal preference of the tertiary amide in the starting material leads to intramolecular migration of a

218 onin were synthesized from readily available starting materials like hydroxyproline, nitrobenzaldehyd

219 Preparation of requisite starting materials, method definition, dipole and dipola

220 a (broad scope, quantitative yield, abundant starting material, mild reaction conditions, and high ch

221 lies in the employment of readily accessible starting materials, Morita-Baylis-Hillman acetates of ac

222 s of DNA for sequencing, the small amount of starting material must be amplified significantly.

223 However, with only metallic starting materials, numerous micron-sized five-component

224 Unlike starting material obtained by chemical synthesis or dire

225 involved a 12,13-olefinic methyl ketone as a starting material obtained by ozonolytic cleavage of epo

226 operties from a single and readily available starting material (OEP) in two straightforward steps, al

227 e quantitative cellular metabolomics using a starting material of 10000 cells.

228 According to our assessment, for starting materials of ~1000 mammalian cells, surface adh

229 ompared to those of the hexasilabenzpolarene starting material on grounds of NMR spectroscopy, X-ray

230 nthesized easily from commercially available starting materials on a multigram scale and are self-act

231 When the starting material possesses a single activated hydrogen,

232 hen beginning with readily available racemic starting materials (racemic products).

233 -position of the benzoxazoles using the same starting materials/reagents.

234 cohol, in the absence of thiourea, or toward starting material recovery when excess thiourea is used.

235 chiral disubstituted allenes from prochiral starting materials remains a long-standing challenge in

236 Moreover, various starting materials required in this protocol are easily

237 newer genomic approaches that require little starting material show great promise to provide an under

238 without the requirement for large amounts of starting material, specific antibodies against proteins

239 y and basicity, through detailed analyses of starting material spectroscopy, addition stereopreferenc

240 and aromaticity up to 2-fold higher than the starting material, strongly suggesting that polymerizati

241 From simple starting materials, structurally complex cyclopentenones

242 recise regiocontrol from simple and abundant starting materials, substrate-directable enantioselectiv

243 The method proceeds from very simple starting materials such as 1,2-diamines and alkyl 3-oxoh

244 Six different classes of key starting materials such as hydroxamic acids, N-hydroxy c

245 The starting materials such as the energy source are easily

246 As inexpensive and versatile starting materials, such compounds continue to influence

247 Regardless of the starting material, sufficient sequence was available for

248 nctional diversity from fixed sets of simple starting materials, suggesting that differentiation of c

249 d in three steps from commercially available starting materials, systematically exploring a typically

250 henotype, function and expansion, as well as starting material T cell repertoire, were analyzed in re

251 ed a nitrile (53%, or 85% based on recovered starting material) that was converted to the eneimide 57

252 the formed E radical anion to the neutral Z starting material the overall transformation is catalyti

253 source, the nature of the graphite (used as starting material), the potassium concentration in the i

254 All rely on the same starting material, the diene diol derived from phenethyl

255 Analysis of the starting material, the T cells collected from the patien

256 Compared to the beta-unsubstituted starting materials, the beta-octahalogenated products we

257 xcellent regioselectivity, readily available starting materials, the broad range of substrates, gram-

258 using B(9)-bromo-meta-carborane as the sole starting material through substrate control.

259 structure efficiently from readily available starting materials through simple operations.

260 gnificantly more expensive and air-sensitive starting material TiCl(3).

261 d acetone was achieved when stirred into the starting material to a final concentration of 70%.

262 RNA-seq (csRNA-seq), which uses total RNA as starting material to detect transcription start sites (T

263 Rice bran was used as a starting material to prepare protein concentrate through

264 yl 5-methyloxazole-4-carboxylate as a single starting material to provide hinduchelins A-D (and unnat

265 1,5-dihydro-2H-pyrrol-2-one (13) as a single starting material to provide hybrubin A in three steps f

266 ess than 1 muL of cell lysate is required as starting material to solve the atomic structure of the u

267 that natural products can serve as powerful starting materials to generate drug substances with nove

268 multaneous kinetic resolution of two racemic starting materials to give one major triazolic diastereo

269 The reaction can use both simple and complex starting materials to produce a range of multifaceted ga

270 cence by using chicken egg white proteins as starting materials to react with aqueous tetrachloroaura

271 substituted triazenes were less reactive as starting materials toward the carbonylative annulation r

272 In the campaign to obtain the acid-starting material, two new natural products, mitchellene

273 of various inexpensive and easily available starting materials under aerobic conditions.

274 niques and providing evidence for the likely starting materials used in beer brewing.

275 ncies (TOF) regardless of the quality of the starting materials used.

276 tly digested milligram amounts of protein as starting material using in-solution digestion protocols

277 ities and enantioselectivities from the same starting materials using a tandem inverse-electron-deman

278 ale from inexpensive, commercially available starting materials using an enantioselective organocatal

279 allylidenebenzofuran from readily accessible starting materials using palladium binaphthyl nanopartic

280 ing different pathways and in racemizing the starting material via formation of an allyl iodide inter

281 The starting material was naturally contaminated Wels catfis

282 ere), the reaction did not proceed, and only starting material was recovered.

283 te with potassium intercalation compounds as starting materials were investigated in depth.

284 ch could be influenced by the ratio of tolan starting materials, were conducted using dicobaltoctacar

285 patterns, consistent with the nature of the starting materials, were obtained.

286 e reactivity of the beta-gamma alkene of the starting material, whereas the e-zeta alkene of the prod

287 increases the library complexity per unit of starting material, which makes it feasible and cost-effe

288 changes of mutants require a large volume of starting materials, which is difficult for unculturable,

289 e Preparation kit (TruSeq) requires abundant starting material while the Takara Bio SMART-Seq v4 Ultr

290 does not require the prefunctionalization of starting material with a leaving group.

291 products to polymers, and represent an ideal starting material with which to forge new connections.

292 ears to be heading in the direction of using starting materials with a significantly lower degree of

293 lecular complexity and diversity from simple starting materials with high atom economy.

294 in 2 to 4 steps from commercially available starting materials with minimal purification.

295 The method couples racemic allyl halide starting materials with sp(2)-hybridized boronic acid de

296 The reaction can be generalized to different starting materials with various substituents on the phen

297 esigned from relatively low-molecular-weight starting materials, with the degree of modification cont

298 In addition, a bicyclic allylic chloride starting material without pseudo-symmetry undergoes a hi

299 uses inexpensive and commercially available starting materials without needing derivatization or the

300 h strand specificity and working with minute starting material, yet until recently there was no kit a