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1 heptaprenol 4 in gram quantities will enable preparative access to key reagents for the study of the
2                                    Access to preparative amounts of discrete charged species allows f
3 o devise a procedure for the purification of preparative amounts of in vivo-synthesized apocatalase.
4 ising approach to quickly and easily produce preparative amounts of proteins.
5 lasma (NTP) is investigated as an innovative preparative analytical technique enabling classification
6 idered as the benchmark stationary phase for preparative and analytical chromatography.
7 or the integration of sample processing with preparative and analytical separations for biology and c
8 uch covalent modifications involve extensive preparative and post-preparative chemistry that poses da
9 e loaded catalyst are in line with a host of preparative and spectral data and with the structures of
10  free-floating products may be a general and preparative approach to access 2D nanomaterials.
11  bionanoparticles in vacuum is potentially a preparative approach to separate heterogeneous mixtures
12               Within this context, different preparative approaches for PDC-NCs as well as some of th
13  been investigated from both mechanistic and preparative aspects.
14  for applications ranging from analytical to preparative bioseparations.
15                                            A preparative biotransamination process has been developed
16 ound in the Athabasca oil sands region using preparative capillary gas chromatography (PCGC) followed
17                                              Preparative capillary gas chromatography (PCGC) is the c
18 n signature of C(ex) added from two sources: preparative capillary gas chromatography (PCGC, C(PCGC))
19  saccharides are one of the central goals of preparative carbohydrate chemistry.
20 e a cellular O-glycome preparation strategy, Preparative Cellular O-Glycome Reporter/Amplification (p
21                                              Preparative centrifugal partition chromatography (CPC) i
22 tions are widespread in nature, yet only one preparative chemical method addresses this challenge in
23                             A combination of preparative chemistry and experimental results from NMR
24 e ligands, a widespread investigation on the preparative chemistry and properties of such compounds h
25 tions involve extensive preparative and post-preparative chemistry that poses daunting limitations in
26 tical when patients receive reduced doses of preparative chemotherapy and/or radiation compared with
27 anced follicular lymphoma by administering a preparative chemotherapy regimen followed by autologous
28  family history or newborn screening, use of preparative chemotherapy, or the type of donor used, did
29 mmunoglobulin were improved after the use of preparative chemotherapy, other immunologic reconstituti
30 e events were consistent with effects of the preparative chemotherapy.
31 00 iU/kg of interleukin-2 to tolerance after preparative chemotherapy.
32 yl-3-hydroxy-4-benzyloxy-5,6-epoxyazepane by preparative chiral HPLC and subsequent elaboration allow
33             Nitrile (+/-)-9 was resolved via preparative chiral HPLC to afford optically pure nitrile
34   This fraction was further purified by semi-preparative chromatography and characterised by HPLC-MS/
35  exoglycosidase digestion arrays, analytical/preparative chromatography and mass spectrometric detect
36 utical applications including analytical and preparative chromatography of organohalogenated species,
37                                              Preparative chromatography of peptides should preferenti
38 ial), including solvent partitioning through preparative chromatography, ranged from approximately 40
39 afforded diastereomers that were resolved by preparative chromatography.
40 f nanoliters and cannot be scaled up for the preparative collection of charge variants.
41 preparation is subsequently fractionated via preparative column chromatography using cellulose-based
42                      We investigated whether preparative combination chemotherapy could replace TBI i
43                            The potential for preparative concentration of DNA is demonstrated using a
44 sence of NK cells is a strong indicator that preparative conditioning is required for engraftment of
45 ansduced with the SIN-gammac vector, without preparative conditioning.
46 lamp and allows for analytical pulse flow or preparative continuous flow reactions.
47 with the low computed barriers, spectral and preparative data show that the reaction is not only poss
48            These studies illustrated the low preparative efficacy of biotransformations and the inabi
49 o our knowledge, migration assay with little preparative effort.
50                                           In preparative electrolysis experiments with a series of al
51 plored through a combination of voltammetry, preparative electrolysis, thiol-electrode modifications,
52  into fronting ones, significantly improving preparative enantiomeric separations.
53                                          Two preparative examples of cross metathesis with the macroc
54 tigram scalable, these transformations are a preparative expansion of the pinane family.
55 lations, and this mechanism was justified by preparative experiments carried out using NiCl(2)/bipyri
56 l chemistry, mass-spectrometric studies, and preparative experiments.
57 ution of chemically dissimilar components in preparative fractionations such as prep TREF (which norm
58 nd stearic (C(18:0)) fatty acids purified by preparative gas chromatography(5-8).
59 s to several analytical approaches including preparative gas chromatography, p-menth-1-en-3-one (pipe
60 n media can mimic the results obtained using preparative gas-phase FVP protocols.
61                                    With semi-preparative GPC the LMWDF (DP3) fractions in the wheat g
62 or either analytical (<50 microg protein) or preparative (&gt;250 microg protein) applications.
63 r. dillenii fruits were fractionated by semi-preparative high-performance countercurrent chromatograp
64                                              Preparative high-performance liquid chromatographic (pre
65 tion of the amino acid hydroxyproline, using preparative high-performance liquid chromatography (Prep
66 PA photolysis products were isolated by semi-preparative high-performance liquid chromatography and i
67 for radiolabeling were obtained using chiral preparative high-performance liquid chromatography and u
68 hydrolysis, acetylation, and purification by preparative high-performance liquid chromatography, and
69 ary chromatographic techniques consisting of preparative high-speed countercurrent chromatography (HS
70 ding counter current chromatography and semi-preparative HPLC due to its low concentration and the pr
71 NHC-containing TM complexes were isolated by preparative HPLC on a chiral stationary phase in good yi
72                                  A two-stage preparative HPLC protocol was subsequently developed for
73 malic acid involved more than 20 steps and a preparative HPLC separation of diastereomeric intermedia
74                    The combination of chiral preparative HPLC separation, VCD measurements, and theor
75  using SPE C-18 cartridges, purified by semi-preparative HPLC then analysed by HPLC/DAD/HRMS in both
76 g intermediates, subsequent fractionation by preparative HPLC, and final hydrogenation.
77 mic isomers, 4a and 4b, were separated using preparative HPLC, and structural analysis and self-aggre
78  The racemic mixture was separated by chiral preparative HPLC, and the resulting lead compound (3R,5S
79 ning all the detected flavonoids obtained by preparative HPLC, in terms of MICs for Staphylococcus au
80           Anthocyanins were isolated by semi-preparative HPLC, weighed, dried, and redissolved in aci
81 G by simple extraction technique followed by preparative HPLC.
82 lowing fractionation of methanol extracts by preparative HPLC.
83 omer was cleanly isolated without the aid of preparative HPLC.
84 alamondin peel was fractionated using a semi-preparative HPLC.
85 ola leaves and flowers were produced by semi-preparative HPLC.
86  diastereomers 7a-1, 7a-2, 7b-1, and 7b-2 by preparative HPLC.
87 ntrifugal partition chromatography (CPC) and preparative HPLC.
88 ere purified by liquid-liquid extraction and preparative HPLC.
89 IVTQTMK and VLVLDTDYK) were fractionated via preparative-HPLC and incubated with MDA at 37 degrees C
90                       This work shows that a preparative IEF method using immobilized pH gradients ca
91                                   Therefore, preparative IEF methods are needed to fractionate charge
92                                 A variety of preparative IEF methods have been developed over the yea
93                                              Preparative immunoprecipitation demonstrated that EpCAM
94 ul tool for the rapid quantification and the preparative immunoseparation of the target proteins.
95                      Owing to its tremendous preparative importance, rhodium carbene chemistry has be
96 omatographic fractionations of extracts from preparative incubations with the 2Z,6E substrate afforde
97                    Here, we have evaluated a preparative irradiation-based method of liver repopulati
98 hemical solvolytic reactivity studied, using preparative irradiations, fluorescence measurements, nan
99                                              Preparative isolation of complex mixtures of compounds f
100 ossible, as well as those who seek advice on preparative issues, up to people having a certain applic
101          Using this approach, we demonstrate preparative labeling under mild conditions for up to ~16
102 ted and purified (>90%) by multi-dimensional preparative LC/MS fractionation.
103                  Unlike previously described preparative LC/MS techniques, we have employed a dynamic
104 ncentration and fractionation of a sample by preparative Liquid Chromatography, identification experi
105  (87 wt.%) were successfully fractionated by preparative liquid chromatography.
106 ation of total body irradiation (TBI) to the preparative lymphodepleting chemotherapy regimen in sequ
107 s potential for increasing overall yields in preparative mass spectrometry is explored briefly.
108                                 By combining preparative mass spectrometry with scanning tunneling mi
109 ion to this problem, viz., a high-efficiency preparative method based on aerobic Co-/ N-hydroxysuccin
110                                     The best preparative method for producing bioactive peptides was
111                                            A preparative method for the synthesis of functionalized 2
112 e amount of included methanol depends on the preparative method used.
113                                 An efficient preparative method was developed for the synthesis of pr
114                                         As a preparative method, FVP is used mainly to induce intramo
115 ules and materials, and despite a variety of preparative methods being available, processes which int
116                                              Preparative methods for stable coatings on smooth substr
117 reports regio- and highly diastereoselective preparative methods for the synthesis of versatile alkal
118                      However, to date, these preparative methods have typically been based on the dir
119  preparation of synthetic ultramarine, using preparative methods that would have been available to al
120                                 We show that preparative methods used previously in studying nucleoso
121                             There were three preparative methods utilized for producing tempe-based p
122                            A series of novel preparative methods were developed to address the proble
123 t will ultimately be determined by efficient preparative methods.
124 n describes structural features, utility and preparative methods.
125 cations in the development of analytical and preparative microfluidic protocols.
126                  The reaction operates under preparative, operationally simple conditions (1 equiv of
127 o compartmentalize and access for integrated preparative or analytical operations on-chip.
128 ure a protein in a complex medium for either preparative or analytical use.
129                       Recent progress in the preparative organic and organometallic chemistry of poly
130 ration procedures and evaluate the different preparative parameters, such as time of saponification,
131 ethyl ester (bis-[60]PCBM) isomer mixture by preparative peak-recycling, high-performance liquid chro
132                                              Preparative photo-oxidation experiments demonstrate that
133                                              Preparative photohydration and trapping reactions by thi
134 nd naphthyl phenols 5-8 were investigated by preparative photolyses in CH3CN-D2O, fluorescence spectr
135 photochemical reactivity was investigated by preparative photolyses, fluorescence spectroscopy, and l
136 y LFP, whereas the adducts were isolated via preparative photolyses.
137                                Steady-state, preparative photooxidation experiments show that aryltri
138  fraction of bikunin GAG mixture obtained by preparative polyacrylamide gel electrophoresis, allowed
139 uired in order to take full advantage of the preparative potential of these transformations.
140                         Key variables of the preparative process (e.g. chitosan and HA molecular weig
141  vetiver essential oil, was subjected to the preparative process, with the scope of isolating two low
142                                            A preparative protein alkaline hydrolysis procedure, as pa
143                                            A preparative protocol, based on the conversion into diast
144 cations ranging from metabolomic analysis to preparative purifications.
145                         Using this approach, preparative quantities of hybrid and complex-type N-glyc
146 ly in expansion of the endosteal niche after preparative radioablation and in the engraftment of dono
147 ic route scouting to identify conditions for preparative reaction scale-up would be a transformative
148                                              Preparative reactions that occur efficiently under dilut
149                              After a uniform preparative regimen (fludarabine 40 mg/m(2) x 5, cycloph
150       The present data show that the Pc 26.1 preparative regimen allows thalassemia patients to safel
151 ts the choice of bone marrow transplantation preparative regimen and can prevent morbidity.
152                                              Preparative regimen and HLH activity affected outcomes,
153 eceiving fludarabine/melphalan (FluMel) as a preparative regimen and patients with unrelated donors (
154  in a clinical setting after a myeloablative preparative regimen for stem cell transplantation, the t
155                                  The optimum preparative regimen for unrelated donor marrow transplan
156 n suggest its potential to become a standard preparative regimen in this population.
157                                          The preparative regimen included busulfan, cyclophosphamide,
158 lantation has been attempted with degrees of preparative regimen intensity, but graft rejection and g
159                             Mice receiving a preparative regimen of nonmyeloablating (5 Gy) total bod
160 hout any statistically significance with the preparative regimen they received.
161            Total body irradiation-containing preparative regimen was the only variable favorably infl
162  Methods Patients received a lymphodepleting preparative regimen, followed by adoptive transfer of pu
163 oduction of novel antileukemia agents in the preparative regimen, maintenance of remission treatment
164 radiation and chemotherapeutic agents in the preparative regimen.
165 d donors, with the use of a nonmyeloablative preparative regimen.
166 ll children were given a fully myeloablative preparative regimen.
167 d a mouse model to investigate the effect of preparative regimens at primary BMT on outcome for secon
168 an increased risk for standard myeloablative preparative regimens based on age (>=50 years), an HSCT-
169                       Further improvement of preparative regimens before allogeneic haemopoietic stem
170 ablative (or reduced intensity) conditioning preparative regimens before haemopoietic cell transplant
171 ummary, recipients of URD-PBSC HCT receiving preparative regimens differing in intensity experienced
172 e added to myeloblative and non-myeloblative preparative regimens for haemopoietic cell transplantati
173 usulfan with total body irradiation (TBI) in preparative regimens for hematopoietic transplantation a
174  in hematopoietic cell transplantation (HCT) preparative regimens for lymphoma.
175                                              Preparative regimens included myeloablative (MA; N = 611
176 tion of chemotherapy and radiotherapy in HCT preparative regimens is not feasible due to dose-limitin
177 hepatocyte transplantation after appropriate preparative regimens may permit sufficient repopulation
178 thymocyte globulin should be included in the preparative regimens of patients with haematological mal
179 nt-related mortality (TRM) were seen for all preparative regimens when CD34(+) cell doses exceeded 4.
180 an be safely combined with reduced-intensity preparative regimens with encouraging results in a singl
181      Results were similar using chemotherapy preparative regimens with or without addition of TBI.
182                                  Advances in preparative regimens, donor selection, and supportive ca
183 nts with contraindications to high-intensity preparative regimens, reduced intensity conditioning sho
184                              Transplantation-preparative regimes were mostly cyclophosphamide with or
185                                        Their preparative relevance is underscored by an application t
186                                              Preparative remote methylene oxidation is obtained in 50
187  coupled cluster level of theory allowed the preparative results to be sorted and an intuitive model
188 on (SPE) using a C18 matrix followed by semi-preparative reverse phase-high performance liquid chroma
189 ion on Amberlite(R) XAD16 polyamide and semi-preparative reverse-phase HPLC columns.
190                We combined NMR spectroscopy, preparative reversed-phase (RP) chromatography, atomic f
191                                        A new preparative route was developed to synthesize new phosph
192       Herein we review the simplicity of the preparative routes available, and their influence over t
193 as the potential to provide more sustainable preparative routes to catalysts than the current multist
194                      A classification of the preparative routes to these synthetic targets according
195 wed by a critical examination of the various preparative routes toward diazaphospholenes.
196                   I and Id were separated by preparative RP-HPLC.
197 yst loadings as low as 0.01 mole percent and preparative scalability (25 grams) are demonstrated.
198 demonstrated by performing the reaction on a preparative scale (88 g).
199  formation of a key advanced intermediate on preparative scale absent any atropisomerization.
200 (I)-catalyzed addition can be conducted on a preparative scale and tolerates a broad substrate scope
201          To identify the oxidation products, preparative scale bulk electrolysis experiments were und
202         This monomer is easily prepared on a preparative scale by a catalytic, enantioselective appro
203  methyl jasmonate (MJ) were isolated at semi-preparative scale by HPLC, using a permethylated beta-cy
204         Here, methodology for the efficient, preparative scale construction of covalent TM complexes
205 ed with an enantiospecific acylase to give a preparative scale dynamic kinetic resolution which allow
206 uction of the Mn(I) center, as observed with preparative scale electrolysis and verified with (13)CO2
207                                          The preparative scale electrolysis generated epoxide-ring-op
208 activity is robust, and PikDH2 was used on a preparative scale for the chemoenzymatic synthesis of un
209  are highly effective; however, their use on preparative scale has minimal precedent because they req
210 ll as peel and fruit pulp were evaluated for preparative scale implementation.
211 sis of Au(102)(p-MBA)(44) nanoparticles on a preparative scale in high yield is described.
212 thod may also be useful to explore on a more preparative scale in the future.
213 te box", has been easily self-assembled on a preparative scale in water, using a template-assisted pr
214 e objective of this research is to implement preparative scale obtention of mangiferin and lupeol fro
215                                              Preparative scale peptide couplings of two N-Boc amino a
216 flavonoid scaffolds and provides a basis for preparative scale production of flavonoid 4 '-O-glucosid
217                                            A preparative scale reaction to deliver 25 g of product is
218                          We also demonstrate preparative scale reductive aminations with wild-type an
219 e spent developing productive analytical and preparative scale separations.
220 hromatographic conditions, and even worse in preparative scale settings.
221 uct inhibition of the evolved enzyme enabled preparative scale synthesis of a single product diastere
222 ied with respect to substrate scope and also preparative scale synthesis.
223 ty (>99.9% de and ee), high yields, and on a preparative scale via benzofuran cyclopropanation with e
224    The reaction has been demonstrated on the preparative scale with 72% isolated yield and 99% Markov
225          Reductions can be accomplished on a preparative scale with as little as 0.05 mol % Ru cataly
226 aphic techniques, both at the analytical and preparative scale, are used also in the identification o
227 h catalyst and microbe, and can be used on a preparative scale, represents a new strategy for chemica
228 catalyzed dimerization can be conducted in a preparative scale, this simple synthesis of trans-1,2-di
229 unusual thermodynamic cycle is employed on a preparative scale, where mechanical energy is used to bu
230 ds for the synthesis of such polymers on the preparative scale.
231 synthesis of the phlorin were performed on a preparative scale.
232 930 TTN and 96% ee), and can be performed on preparative scale.
233 94 % ee; >98 % de) and can be performed on a preparative scale.
234 high levels of enantioselectivity, even on a preparative scale.
235 e at promoting the cyclization reaction on a preparative scale.
236 [2',2',3'-(2)H(3)]-solifenacin fumarate on a preparative scale.
237 olubility of 4 prevented its resolution on a preparative scale.
238  synthetic tool for accessing materials on a preparative scale.
239 n the bioanalytical space, especially at the preparative scale.
240 eric excess), and can be performed easily on preparative scale.
241  and C-S bonds in chemoenzymatic cascades on preparative scale.
242 he utility of the system was demonstrated by preparative-scale applications.
243                                              Preparative-scale aziridinations can be easily achieved
244                                          The preparative-scale catalytic aminooxygenation reaction (g
245                     Strategies for optimized preparative-scale electrolyses may then be devised on th
246                                              Preparative-scale electrolyses showed that carbon monoxi
247 f methanol or formate could be detected upon preparative-scale electrolysis of CO2 on the same electr
248 extraction, flash column chromatography, and preparative-scale high performance liquid chromatography
249 dition (InCl(3), 0.32 mM) was performed on a preparative-scale providing the 5-isocorrole in an isola
250                                            A preparative-scale reaction to deliver >90 mmol of produc
251                                         In a preparative-scale reaction, unreacted (S)-(+)-butanoate
252 s often a limitation in adopting enzymes for preparative-scale synthesis, reaction with demanding sub
253                                      A novel preparative-scale triple gas chromatographic system, equ
254 providing a powerful tool when deployable on preparative-scale.
255 s to the desired hydroxylated derivatives at preparative scales (0.4 g) and in high isolated yields (
256  asymmetric methods have seen limited use on preparative scales (more than a gram).
257 ubstituted derivatives can be synthesized on preparative scales, using a chemoenzymatic approach.
258 mbered ring systems stereoselectively and on preparative scales.
259 r concentration of the polyphenols from PSP, preparative separation into two fractions, designated an
260                                              Preparative separation of membrane protein loaded nanodi
261 superior performance for both analytical and preparative separation of various physiologically releva
262    Counter-current chromatography (CCC) is a preparative separation technique working with the two li
263 ility" and therefore has great potential for preparative separations.
264 ficant production rate improvements in (semi)preparative SFC.
265  from a water extract of Se-rich yeast using preparative size exclusion, anion exchange, and capillar
266   The mAb HMW fractions were collected using preparative size-exclusion chromatography (SEC) and exte
267 or types and their successful application in preparative solar syntheses.
268                                   All sample preparative steps including magnetic stirring assisted D
269  (MALDI-ToF), REIMS based methods require no preparative steps nor time-consuming cell extractions.
270 g data, are nonetheless dependent on various preparative steps to generate DNA fragments of required
271 hondrial activity and efficiency, and, after preparative steps, it takes 6-8 h to complete.
272 linical laboratories without any preanalysis preparative steps.
273 n be obtained from commercial sources in two preparative steps.
274 ite materials, critically examine the viable preparative strategies geared to craft intimate CP-NC na
275 cal synthesis of AMPDs, through nanoparticle preparative strategies, to the most recent applications
276                    Finally, we demonstrate a preparative strategy for obtaining pure bioorthogonally
277 entary methods: a MALDI-MS method and a semi-preparative sub-fractionation.
278 ic trans-dinaphthyl isomers were resolved by preparative supercritical fluid chromatography (SFC) on
279             Also, at low ethylene pressures, preparative syntheses of several 2,3-disubstituted 1,3-b
280 anding ketones and amines, which include the preparative synthesis of N-substituted beta-amino ester
281 ed solution that is more characteristic of a preparative synthetic reaction.
282 ent evolution of a multidimensional GC-GC-GC preparative system, now combined with an online LC prese
283                                         With preparative tandem affinity purification followed by MS
284 ayer-compression mechanism revealed a simple preparative technique to produce nanosheets in 95% overa
285 F-enzyme composites with special emphasis on preparative techniques and the synergistic effects of en
286                                              Preparative therapy for the transplant consisted of high
287                           The application of preparative thin layer chromatography-2,2-diphenyl-1-pic
288 so partially epimerized to arborisidine upon preparative TLC purification (eluent: MeOH/CHCl(3) satur
289 n mass spectrometry based proteomics or as a preparative tool for analyte purification, fractionation
290      At week 12, LDL-C reduction measured by preparative ultracentrifugation (least squares mean [sta
291 xylate carbene series that enjoys widespread preparative use, or to the class of mononuclear half-san
292                           To demonstrate the preparative utility of this method in the context of bio
293 onalization, few intermolecular processes of preparative value exist.
294 pot operations that significantly extend the preparative value of diene-transmissive Diels-Alder sequ
295    Separations can be broadly categorized as preparative, where the objective is to extract purified
296 ing materials has facilitated the underlying preparative work.
297 xy-6,6-dimethylbicyclo[3.1.1]heptan-2-one in preparative yield (65% on a multigram scale).
298 xides, giving quantitative conversions, high preparative yields and excellent chemoselectivity.
299 able catalyst-controlled site-selectivity in preparative yields over a range of topologically diverse
300 didichlorophosphorylated diamondoids in high preparative yields.

 
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