ライフサイエンスコーパス: synthesis

1 nsferase genes involved in exopolysaccharide synthesis.

2 ators after they are incorporated during RNA synthesis.

3 GAT1) are already known to be related to oil synthesis.

4 correlated with genes involvement in oxalate synthesis.

5 roles in regulating fragile X protein (FMRP) synthesis.

6 ation initiation and reducing global protein synthesis.

7 analog widely employed in studies of protein synthesis.

8 rug discovery programmes and natural product synthesis.

9 ding to PHGDH degradation to suppress serine synthesis.

10 te shift likely has little effect on protein synthesis.

11 could be connected to C. neoformans melanin synthesis.

12 ure more efficient and practical for organic synthesis.

13 ELOVL2 (Elovl2(-/-) ), the key enzyme in DHA synthesis.

14 tors) and regulates crucial steps in protein synthesis.

15 ansformations in the field of modern organic synthesis.

16 to stationary phase, tone down their protein synthesis.

17 s provides a continual challenge to chemical synthesis.

18 regulate hepatic acetyl-CoA and cholesterol synthesis.

19 nfection, which was reversed by blocking LOS synthesis.

20 an essential amino acid required for protein synthesis.

21 and unnatural-amino-acid-containing protein synthesis.

22 rapid cell elongation to secondary cell wall synthesis.

23 rised by reduced or absent beta-globin chain synthesis.

24 rch for exoplanets(14,15), optical frequency synthesis(16), time keeping(17) and other areas(10).

25 6 genes were found to be associated with oil synthesis (27 genes), amino acid synthesis (four genes)

26 we isolated multiple genes impacting protein synthesis: a ribosomal RNA helicase gene, tRNA biosynthe

27 The Pif1-dependent stimulation of DNA synthesis across strong protein barriers may be benefici

28 the basis of this detection, our population synthesis analysis implies that such asymmetric binaries

29 at the two paramount sources of bias are the synthesis and amplification (PCR) processes.

30 c olefins remains the pinnacle of asymmetric synthesis and an unsolved challenge.

31 tion risk during the colder periods when AMP synthesis and bacterial growth is slow and pathogen pres

32 cyltransferase (LRAT) disrupt 11-cis-retinal synthesis and cause Leber congenital amaurosis (LCA).

33 The synthesis and characterization of a series of light-driv

34 c acid and non-nucleic acid targets, ease of synthesis and chemical modification, amenability to be i

35 Here, we describe the synthesis and conformational analysis of three delta-aza

36 g, and could be particularly relevant to the synthesis and cotranslational behavior of some proteins.

37 s are determined by the balance between mRNA synthesis and decay.

38 Overall, synthesis and degradation made equal contributions to th

39 The contribution of each mechanism to cutin synthesis and deposition has shown a temporal and coordi

40 Herein we present the synthesis and evaluation of anion-binding properties of

41 Herein, we describe the synthesis and evaluation of immunotherapeutic liposomal

42 Innovations in soft material synthesis and fabrication technologies have led to the d

43 for translational tuning to balance protein synthesis and folding.

44 ted prolonged S-phase, were defective in DNA synthesis and had increased DNA damage levels, suggestin

45 d through a variety of substrates, including synthesis and late-stage functionalization of scaffolds

46 mong the most fundamental tasks in inorganic synthesis and materials science.

47 d utility of this method for target molecule synthesis and medicinal chemistry.

48 hich may contribute to the overall septal PG synthesis and regulation during cell division.

49 luding phosphatidylinositol-3,5-bisphosphate synthesis and retrograde transport from the vacuole.

50 his effect of mTORC1/2 inhibitors on protein synthesis and RRM2 levels was rescued in cell lines with

51 This review is devoted to the synthesis and structure-activity relationships (SAR) of

52 elegans COQ-2e is required for efficient RQ synthesis and survival in cyanide.

53 e characterized by elevated rates of protein synthesis and that high expression of ABCE1, a translati

54 ts into the processes that underpin osmolyte synthesis and transport, but the main computational appr

55 sponded differently to XRN1 deletion in mRNA synthesis and were differentially regulated by mRNA deca

56 NTR sequences regulate RNA synthesis and, by analogy with other segmented negative-

57 se changes presumably lead to decreased 5-HT synthesis and/or increased 5-HT reuptake, thereby reduci

58 We report here the design, synthesis, and biological characterization of a series o

59 Herein, we report the design, synthesis, and biological evaluation of a series of new

60 Here we report the design, synthesis, and biological evaluation of several close-in

61 Herein, we describe the design, synthesis, and characterization of new dual inhibitors o

62 We describe our design, synthesis, and chemical study of a set of functional epi

63 dology enables spatial regulation of protein synthesis, and deciphering, reconstruction and design of

64 of innovative tools, we examine the design, synthesis, and properties of light-activated degraders.

65 ated ECT2 recruitment to rDNA, elevated rRNA synthesis, and transformed growth.

66 f chemistry, and efficient methods for their synthesis are continually desired.

67 Key to the synthesis are stereocontrolled 1,4-semihydrogenation of

68 nstrate a promising application of BO in CNT synthesis as an efficient and robust algorithm which can

69 d it appears to limit the rate of processive synthesis at 4 degrees C.

70 We perform a comprehensive analysis of DNA synthesis at all STR permutations and interrogate the im

71 ent cohesin removal is needed to restart DNA synthesis at stalled forks and promote survival followin

72 Pharmacological inhibition of GT1b synthesis attenuates nerve injury-induced spinal cord mi

73 Nanocrystals from the same synthesis batch display what are often presumed to be sm

74 on is an important building block in organic synthesis because it features several reaction sites wit

75 y decreased 40S fraction and reduced protein synthesis but no major changes in m(2) (6,6)A levels in

76 were mechanistically independent of protein synthesis but sensitive to pharmacological blockade of t

77 morphogen SpmX defines the site of stalk PG synthesis, but SpmX is a PG hydrolase.

78 ent plasma cells adapt to increased antibody synthesis by activating the unfolded protein response (U

79 tide addition, can stimulate translesion RNA synthesis by Escherichia coli RNAP without altering the

80 me assembly factor, RbfA, suppresses protein synthesis by immature Escherichia coli 30S subunits.

81 We now demonstrate that inhibiting NAA synthesis by intracisternal administration of a locked n

82 ed off of biosynthetic machinery for terpene synthesis can be used to arrive at Taxol.

83 )F]DOPA uptake, an estimate of dopamine (DA) synthesis capacity, in the striatum predictive of conver

84 ]DOPA PET scan to quantify striatal dopamine synthesis capacity.

85 icarboxylic acid (TCA) cycle, and amino acid synthesis/catabolism.

86 1, slo-1, or homt-1 (a gene required for Mel synthesis) causes substantially increased neurotransmitt

87 The synthesis characterization and theoretical analysis of t

88 The ability to achieve chirality-selective synthesis (chiral induction) is of great importance in s

89 to previously unattainable measurements and synthesis conditions at unparalleled efficiencies and sa

90 substrate lickings) when presented with the synthesised cyclo(L-Pro-L-Pro) chemical blend, compared

91 a large set of single-cell E. coli flagellar synthesis data from different strains and mutants, we id

92 We find that mitochondrial ATP synthesis decreases by approximately 50% during early mi

93 are ultimately responsible for the excessive synthesis, deposition and remodelling of extracellular m

94 pe reactions commonly applied for on-surface synthesis, distinct stepwise on-surface reactions, inclu

95 lational modification that regulates protein synthesis during cellular response to oxidative stress.

96 ion of BA transporters and BA detoxification/synthesis enzymes in KO/KD compared with KO alone.

97 , the rate-limiting substrate for fatty acid synthesis (FAS), is produced in the soma and delivered t

98 al. show how oncogene-driven fatty-acid synthesis favors Treg cells over effector T cells and ho

99 eotide was in the first coding position, DNA synthesis fidelity was similar to that observed with a 1

100 ed with oil synthesis (27 genes), amino acid synthesis (four genes) and the tricarboxylic acid (TCA)

101 Decreased PE synthesis from loss of EPT1 or PSD1 and PSD2 leads to do

102 The generation of synthesis gas (hydrogen and carbon monoxide mixture) fro

103 the division of labor during leading-strand synthesis generally.

104 sins (ebh, sdrD), polysaccharide and capsule synthesis genes, cell wall remodeling genes (lytN, ddh),

105 Template-directed synthesis has been used to prepare a fully pai-conjugate

106 and society, and recent improvements in DNA synthesis have enabled the manipulation of megabase geno

107 tially valuable building blocks for chemical synthesis, have each been prepared from cyclopentanone i

108 e to dopaquinone, thereby initiating melanin synthesis, i.e., melanogenesis.

109 ing mitochondrial redox potential and/or ATP synthesis impaired proline biosynthesis.

110 strate the feasibility of perturbing protein synthesis in a mouse liver by targeting translation elon

111 of the loss of ribosome recycling on protein synthesis in E. coli.

112 r cells require nominal increases in protein synthesis in order to maintain high proliferation rates.

113 y transcription factor required for cytokine synthesis in psoriasis.

114 Here, we find that cAMP synthesis in response to elevated glucose and the select

115 nzyme IIb, which is required for amylopectin synthesis in the endosperm.

116 Pretreatment with a glucocorticoid synthesis inhibitor blocked the memory enhancement as we

117 and has hampered integration of phospholipid synthesis into artificial cells.

118 ssential enzyme in the initiation of protein synthesis, into large bundles of filaments.

119 We propose that Myc-regulated fatty acid synthesis is a valid target for therapy and/or preventio

120 Automated chemical oligosaccharide synthesis is an attractive concept that has been success

121 in machines extract these lipids after their synthesis is completed at the inner membrane and transpo

122 hanism by which virulence is regulated by PE synthesis is only partially understood.

123 Understanding how their synthesis is regulated is crucial to revealing these lip

124 How sphingolipid synthesis is regulated to fulfill these physiological re

125 The key strategy used for this novel synthesis is the facile one-step construction of a spiro

126 ish revealed that neutrophil chemoattractant synthesis is triggered by a sustained calcium flux upon

127 l erythritol phosphate pathway of isoprenoid synthesis, is essential for Gram-negative bacteria, myco

128 is the ability of a gene to repress its own synthesis, is the most abundant regulatory motif known t

129 The cell-wall-synthesis machinery responsible for rod shape in Escheri

130 motifs, control experiments, and gram-scale synthesis make the synthetic model viable and significan

131 rminal differentiation (FLG and FLG2), lipid synthesis/metabolism (ELOVL3 and FA2H), and tight juncti

132 Here we demonstrate a gas-phase synthesis method that substantially transforms the struc

133 uate the response of skeletal muscle protein synthesis (MPS) to anabolic stimuli such as protein inge

134 Reported herein is a total synthesis of (+)-6-epi-ophiobolin A in 14 steps, a task

135 t reorganize its catalytic center to promote synthesis of 2'-5'-oligoadenylate and thus activation of

136 A facile and efficient method for the synthesis of 3-[(4-nitrophenyl)thio]-substituted 4-methy

137 on has a broad scope, as demonstrated by the synthesis of 35 different ketones bearing a wide variety

138 Systematic review and synthesis of 61 qualitative studies and two systematic r

139 We also establish synthesis of 8-hydroxygeraniol, the precursor of monoter

140 One of the direct outcomes on the first synthesis of a complete set of cation derivatives is to

141 Careful synthesis of a fluorenylmethyloxycarbonyl- and trityl-pr

142 ic DNA transcription templates regulates the synthesis of a fluorescence-activating RNA aptamer.

143 The synthesis of a new tetraborylethylene (TBE) is reported,

144 of this method has been demonstrated in the synthesis of acylsilanes bearing different silyl groups

145 environment was exploited to accomplish the synthesis of alkenes using a one-pot, two-step experimen

146 We report the synthesis of all-cis 1,2,4,5-tetrakis (trifluoromethyl)-

147 ) catalyzed the direct or one-pot sequential synthesis of alpha,alpha-disubstituted ketones via the a

148 The synthesis of aryl thioether through the cross-coupling o

149 An atom- and step-economic synthesis of aryliminophosphoranes bearing ortho urea wa

150 Challenges to the de novo synthesis of bacteriochlorophyll a (BChl a), the chief p

151 -pot, metal-free, double cyclization for the synthesis of bicyclic 2-pyridones as peptidomimetics was

152 Application to the synthesis of bioactive, pyrrolizine-fused 4-quinolinone,

153 Herein, we describe how a biomimetic synthesis of bruceol, a pentacyclic meroterpenoid, led t

154 s at fully substituted carbon centers in the synthesis of chiral 2,2-disubstituted benzomorpholines.

155 iated methodology has been developed for the synthesis of chiral 2-aryl-ferroceneamides from chiral 2

156 products are suitable intermediates for the synthesis of chiral vicinal diamines as has been verifie

157 and can be employed to achieve the targeted synthesis of clinically-relevant molecules in the presen

158 tudy reveals an alternative sequence for the synthesis of compounds that contain the pyrrolodiketopip

159 reversible C-C single bond formation for the synthesis of crystalline 2D CPs.

160 rganozinc reagents, thereby allowing for the synthesis of cyclic and acyclic tetrasubstituted double

161 However, performing robust synthesis of data from pharmacogenetic studies is often

162 s highlight the utility of the method in the synthesis of densely functionalized small molecules suit

163 A convenient additive-free synthesis of dihydro-4H-1,2-oxazines via a Cloke-Wilson-

164 This general synthesis of diverse two-dimensional vdWH arrays provide

165 The enzymatic synthesis of DNA is a promising alternative, but thus fa

166 ction may be useful in biotechnology for the synthesis of drugs or small molecules.

167 re, we have extended this methodology to the synthesis of enynes.

168 The reaction has been applied to the synthesis of fluorinated analogues of diltiazem and tiaz

169 sed as an initiator, was tracked through the synthesis of Glu-PLGA by both (13)C NMR and enzymatic an

170 in organic solvent as well as the enzymatic synthesis of glycan epitopes in the aqueous phase in a s

171 The synthesis of graphene nanoribbons (GNRs) that contain si

172 alyzes the rate-limiting step in the de novo synthesis of guanine nucleotides, impacting the cellular

173 Herein, we describe an expeditious total synthesis of hemiasterlin featuring a four-component Ugi

174 Consistent with its role in the synthesis of heparan sulfate, we show that this activity

175 d cross-coupling amendable for the efficient synthesis of heteroaromatic substrates.

176 nditions and broad scope, and allows for the synthesis of highly functionalized azetidines from readi

177 oid, led to the anticipation, isolation, and synthesis of isobruceol.

178 otensin system (RAS), including the balanced synthesis of its main effector peptides Ang (angiotensin

179 supplementation, indicating that endogenous synthesis of LA is essential for C. elegans development.

180 is a unified click-approach for the modular synthesis of lead-like structures through application of

181 ir target mRNAs were predicted to involve in synthesis of melanin, carotenoid or tetrapyrrole.

182 identify a pre-emptive pathway that reduces synthesis of membrane proteins that have failed to prope

183 An asymmetric total synthesis of Merck's hNK(1) antagonist and three of its

184 The synthesis of metallo-supramolecular systems with well-de

185 We sought to optimize the synthesis of MH microneedles (MHMs) while maintaining th

186 ties at the 2- and 7-positions, allowing the synthesis of mixed/asymmetric derivatives.

187 ld open new possibilities for the design and synthesis of molecular cages with novel topologies targe

188 Our molecular tuning allowed for the synthesis of molecules exhibiting strong visible-range a

189 substrates and enzyme activities towards the synthesis of monolignols.

190 ecent methodological study investigating the synthesis of N-alkoxyazomethine ylides, an unexpected am

191 h-throughput, printing-technology-compatible synthesis of nanocrystalline particles of common materia

192 tive bottom-up approach for the non-covalent synthesis of nascent axial organic heterostructures, whi

193 he regulatory events that control the timely synthesis of Ndc80.

194 This strategy led to the synthesis of new conformationally restrained boron-methy

195 This is a qualitative synthesis of new evidence with existing meta-analyses, a

196 monoesters to diesters may have enabled the synthesis of nucleic acids, perhaps opening a way into t

197 start with a brief primer on the biological synthesis of nucleotides, followed by an extensive focus

198 The strategy is useful for the synthesis of other structurally related complex glycans.

199 To facilitate the synthesis of paromomycin and/or neomycin analogues, we d

200 ized silica resin to facilitate the chemical synthesis of peptides in organic solvent as well as the

201 lic acid-phosphoric acid anhydrides, for the synthesis of peptidyl-RNAs, peptides, RNA oligomers and

202 involving lipid metabolism, specifically the synthesis of pigments and oxylipins, and the metabolism

203 be derivatization via direct metalation, but synthesis of polysubstituted thiophenes bearing reactive

204 represents a new and powerful method for the synthesis of porous solids with tailored functionalities

205 There is no recent synthesis of primary research studies into older people'

206 omical and scalable route for the controlled synthesis of Pt-based intermetallic catalysts, which can

207 Here, we describe a total synthesis of PvD(1), the defensin from the common bean P

208 A tandem synthesis of quinazolinones from 2-aminobenzonitriles is

209 The synthesis of RA requires two enzymatic reactions: oxidat

210 d coordination (ACC) strategy to achieve the synthesis of rare-earth single erbium (Er) atoms support

211 the components of nucleotides-either via the synthesis of ribose and the canonical nucleobases and th

212 Review and synthesis of selective literature, with interpretation a

213 and offers a fresh template strategy for the synthesis of silver NCs with high symmetry.

214 ls by one-pot heterocyclization and into the synthesis of six-membered azaheterocycles.

215 observation was additionally verified by the synthesis of stable CO and 2,6-xylylisocyanide (XylNC) a

216 rk, a novel strategy for the straightforward synthesis of substituted phthalimides is described, whic

217 In this article, a high-yield method for the synthesis of sulfonyl 9-fluorenylidenes is described, wh

218 ere we report a strategy that simplifies the synthesis of terpenes by inverting the order of nature's

219 in the most brief and highest yielding total synthesis of the alkaloid in three steps and a 36% overa

220 esis uses key intermediates in the prebiotic synthesis of the canonical pyrimidine ribonucleosides (c

221 We report the design and synthesis of the compounds and binding results for the J

222 ic substitution leading to a stereoselective synthesis of the compounds of interest.

223 scientific statement provides an up-to-date synthesis of the existing data on the MT and how it rela

224 An enantioselective total synthesis of the labdane diterpene andrographolide, the

225 The strategy is exemplified by the synthesis of the marine natural product (+)-bretonin B.

226 the predominant pathways responsible for the synthesis of the most abundant phospholipids, phosphatid

227 ycosyltransferase activities involved in the synthesis of the N-glycan of the viral major capsid prot

228 successfully applied as the key step in the synthesis of the natural product lamellarin R.

229 ated, the pyrimidines persist throughout the synthesis of the purine deoxyribonucleosides, leading to

230 o-, regio- and furanosyl-selective prebiotic synthesis of the purine deoxyribonucleosides: deoxyadeno

231 pairment, warranting a timely evaluation and synthesis of the scientific literature and formulation o

232 E-6-PHOSPHATE SYNTHASE1 (TPS1) catalyzes the synthesis of the sucrose-signaling metabolite trehalose

233 te their hydrological significance, a global synthesis of their effects on hydrology is lacking.

234 The synthesis of these materials by impregnation from strong

235 The reactions afford the synthesis of two open-shell nanographenes (1a and 1b) ex

236 nimide removal by Pd(II) was applied for the synthesis of two ubiquitin activity-based probes (Ub-ABP

237 g the electrodeposition conditions can allow synthesis of unlimited combinations of ligand nano-seque

238 products and drug molecules, stereospecific synthesis of useful alpha-chiral alkyl amines, and rapid

239 the current strategy may be suitable for the synthesis of various complex natural and unnatural cyclo

240 In this work, we demonstrate the first synthesis of vinylene-linked 2D CPs, namely, 2D poly(phe

241 Herein, a metal-free domino synthesis of Z-selective alpha,beta-diphenylthio enones

242 inefficient removal of HFA from the site of synthesis on phosphatidylcholine (PC).

243 ered serotonin was not due to either reduced synthesis or increased breakdown capacity.

244 d with inhibitors that prevent peptidoglycan synthesis or peptidoglycan crosslinking by penicillin-bi

245 orted molecular imaging measures of dopamine synthesis or release capacities, dopamine D(2/3) recepto

246 tion of exchangeable oxygen during cellulose synthesis (P(ex) ) was kept constant.

247 ression of genes involved in the cholesterol synthesis pathway in primary human T-ALL specimens.

248 We have synthesised photoswitchable paclitaxel-based microtubule

249 ally in chemical biology for peptide/protein synthesis, posttranslational modifications, and DNA labe

250 The label-free and sensitive detection of synthesis products from single microbial cells remains t

251 The classification, synthesis, properties and applications of dually modifie

252 elegans and human cancer cells, ether-lipid synthesis protects against ferroptosis.

253 expand DEL reactivity using standard organic synthesis protocols.

254 We maintain that our synthesis provides a state-of-the-art analysis of patter

255 For a deeper understanding of the levan synthesis reaction, we determined the crystallographic s

256 ion facilitates the increase in nucleic acid synthesis required for anabolic cell growth and prolifer

257 o demonstrate that cytokinin-induced protein synthesis requires isoforms of the ribosomal protein L4

258 olvents commonly used in polymer and peptide synthesis results in the alteration of DNA helical struc

259 g DNA replication, transcription, nucleotide synthesis, ribosome biogenesis and function, as well as

260 However, conventional synthesis routes to produce such ceramic NWs have prohib

261 single, systemic dose of methotrexate, a DNA-synthesis (S phase) inhibitor, has been used since 1991

262 bility in compositional tuning and immediate synthesis scalability of high-Ni NMA very similar to NCA

263 )T(M) recall response because of expeditious synthesis/secretion kinetics (CCL3/4/5) and low activati

264 ress made in the field of small fluorocarbon synthesis since their invention in the early 1930s by Th

265 Its present synthesis still relies on an energy-intensive thermal tr

266 Using a function-oriented synthesis strategy, we designed, synthesized, and evalua

267 DNA-templated synthesis takes advantage of the programmability of DNA-

268 growth pathways in vapour- and liquid-phase synthesis techniques.

269 viding a framework for the design of new DEL synthesis technologies to enable next-generation drug di

270 ta and also allows for future sequencing and synthesis technologies, by changing the parameters of th

271 that we describe, depending on the metal and synthesis temperature used, as random (Co, Cd, 120 degre

272 the regulation of mRNA stability and protein synthesis through posttranscriptional mechanisms.

273 ural analyses of replicative and translesion synthesis (TLS) DNA polymerases (Pols) are retained in t

274 the germline; there it is used in fatty acid synthesis to critically support embryonic development.

275 e and robust body of literature suitable for synthesis to detect macroimmunology patterns and effect

276 ioinformatic algorithms followed by chemical synthesis to predict and then produce small molecules in

277 PHGDH overexpression activates serine synthesis to promote cancer progression.

278 believed to chaperone Q(6) from its site of synthesis to the respiratory complexes.

279 sule polymerase Cps1B of App1 as an in vitro synthesis tool and an alternative for capsule polymer pr

280 ernative that can potentially enable ammonia synthesis under milder conditions in small-scale, distri

281 Our synthesis uses key intermediates in the prebiotic synthe

282 for individual SHs are scarce because probe synthesis usually takes place by time-consuming solution

283 translational machinery to slow down protein synthesis via phosphorylation of the eukaryotic initiati

284 The partial reduction of ECm during RNA synthesis was circumvented by the protection of the nitr

285 The results demonstrated that protein synthesis was modulated to facilitate protein secretion

286 or HDAC3/6-selective HDACi, and new protein synthesis was not required for gene suppression by HDACi

287 zes with DA vesicles and is necessary for DA synthesis, was assessed across the sample.

288 drogenase, an enzyme required for 15-Oxo-ETE synthesis, was predominantly expressed in mast cells and

289 By re-engineering peptidoglycan synthesis, we have constructed a continuous spectrophoto

290 d in DNA packaging, replication, and protein synthesis were detected at lower rates and zinc finger f

291 While ribosome biogenesis and global protein synthesis were unaffected by nsun-1 depletion, translati

292 ficial larynx sound source, a vowel sound is synthesised which compares favourably with vowels of mod

293 h the natural A, T, G and C bases during DNA synthesis, which allows for labeling of replicating or r

294 egulation of genes responsible for cell wall synthesis, which contributes to fibre length by modulati

295 e is limited, EpdSCs activate de novo serine synthesis, which in turn stimulates alpha-ketoglutarate-

296 s associated with increased rates of protein synthesis, which lead to growth inhibition and hypersens

297 been proven as a powerful tool in asymmetric synthesis, while flow chemistry has begun its rise as a

298 ses lies in the mechanisms that balance mRNA synthesis with mRNA decay.

299 The GQDs are successfully synthesised with a high yield of over 84%, the highest v

300 We report the synthesis, X-ray crystal structure, and molecular recogn