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1 ng L(-1) (conjugated), and 0.18-18 ng L(-1) (halogenated).
2 ntheses and full characterization of two new halogenated 1,1-diamino-2,2-dinitroethene (FOX-7) compou
3 y in situ NMR spectroscopy, which revealed C-halogenated 1,2-bis(dibromoboryl)benzenes to be the key
4 yl bond-forming process for the synthesis of halogenated 2-amino-2'-hydroxy-1,1'-biaryls that are cur
5 uX2 (X = Cl, Br) provided exclusive di-ortho-halogenated 2-arylbenzothiazoles.
6 giving straightforward and general access to halogenated 3,5-diaryl- and alkylarylisoxazoles, pyrazol
7  with MesMgBr yields air- and water-stable C-halogenated 9,10-dimesityl-DBAs (2-Br-6,7-Me2-DBA(Mes)2;
8 olved halogenase enzymes to regioselectively halogenate a diverse range of biosynthetic precursors, w
9 ogenase RadH can be used to regioselectively halogenate a range of bioactive aromatic scaffolds.
10                                          The halogenated acetic acids (HAAs) are generally considered
11 ation capacity of the system was tested with halogenated acetic acids and halogenated aromatic compou
12 yclohex-2-en-1-ones with the easily prepared halogenating agent BnNMe(3).ICl(2) in MeOH-CH(2)Cl(2).
13 d Br) bonds without addition of any external halogenating agent via cascade sulfenylation-halogenatio
14  coupling of C(sp(2) )-H bonds, alkynes, and halogenating agents to give alkenyl halides is reported.
15 mpounds that modulate GluD2(LC), including a halogenated alanine analog as well as the kynurenic acid
16 veloped based on the enzymatic reaction with halogenated aliphatic hydrocarbons that is accompanied b
17 genated heterocyclic aromatic compounds, and halogenated alkanes.
18                                              Halogenated alkenes are a class of anthropogenic substan
19 rect approach involving the hydroboration of halogenated alkenes is impeded by partial dehalogenation
20 nt Suzuki-Miyaura cross-coupling reaction of halogenated aminopyrazoles and their amides or ureas wit
21  of the benzotriazole unit by preparation of halogenated analogues and Suzuki-Miyaura cross-coupling
22 ene exhibits critical speeding up, while the halogenated analogues display critical slowing.
23                   Dec604 CB and other lesser halogenated analogues of Dec604 show greater bioaccumula
24                                   The highly halogenated and most abundant PBDEs and AFRs in air also
25 arbonyl groups (pathways a, b) as well as at halogenated and nonhalogenated conjugate positions (path
26 esults emphasize the increasing relevance of halogenated and nonhalogenated OPEs as contaminants in t
27            Overall, 54 organics including 26 halogenated and oxygenated alkanes, 8 alkenes, and 20 al
28                                   Identified halogenated and oxygenated electrolysis products typical
29 ription factor that mediates the toxicity of halogenated and polycyclic aromatic hydrocarbons in vert
30 yl group bound to a carrier protein is first halogenated and then elaborated by peptidic or polyketid
31 dance and distribution of genes encoding for halogenating and dehalogenating enzymes in a German fore
32  broad range of unactivated pyridines can be halogenated, and the method is viable for late-stage hal
33 This is the first experimental evidence that halogenated anesthetics can directly undergo quantum int
34 e potassium channel function is activated by halogenated anesthetics through binding at a putative an
35       Here we describe the transformation of halogenated anilines, benzonitriles, phenols, methoxylat
36 lcarbmates that can further be hydrolyzed to halogenated anilines.
37 herwise difficult to obtain 2,3- and 2,3,6,7-halogenated anthracenes with diverse east/west substitue
38 roved to be an efficient approach to dispose halogenated aromatic compounds (HACs).
39 ntaminant structures, including nitrated and halogenated aromatic compounds, halogenated heterocyclic
40 was tested with halogenated acetic acids and halogenated aromatic compounds.
41                                              Halogenated aromatics are one of the largest chemical cl
42         Examples include long-chain alkanes, halogenated aromatics, and cyclic volatile methylsiloxan
43  present in a multitude of commercially used halogenated aromatics.
44 approach using a Chan-Lam coupling between a halogenated aryl pinacol boronate ester and an aryl meth
45 lladium-catalyzed cross-coupling reaction of halogenated azines with organozinc derivatives of ferroc
46 ,2-dinitroethene (FOX-7) compounds and three halogenated azo-bridged FOX-7 derivatives are described.
47 V vs. SCE) sufficient to oxidize benzene and halogenated benzenes via single-electron transfer (SET),
48 izes isotopically distinct benzothiazine and halogenated benzothiazine probes to sequentially alkylat
49         In summary, we demonstrate here that halogenated benzothiazine-based alkylating agents can be
50  the pathway to synthesize a series of novel halogenated benzoxazoles.
51      Mono(2-ethylhexyl) tetrabromophthalate, halogenated bisphenols and phenols, and hydroxylated PBD
52 terize and compare the ultrafast dynamics of halogenated BODIPY chromophores through applying two-dim
53                                              Halogenated BODIPY photoredox catalysts were additionall
54                                    Our novel halogenated BODIPY-tetrazine probes only become efficien
55             We also report the generation of halogenated bruceol derivatives and the synthesis of sev
56  of nucleic acid complexes containing either halogenated building blocks or halogenated ligands.
57 ns can be used to prepare potentially useful halogenated building blocks.
58                                 Identifiable halogenated byproduct formation and accumulation was min
59 t approaches are likely necessary to prevent halogenated byproducts in the treated water.
60  results demonstrate the occurrence of novel halogenated byproducts of PPCPs that have limited toxico
61 nor reacted with the halogen species to form halogenated byproducts.
62 stingly, AmbP3 also accepts hapalindole A, a halogenated C-10 epimer of hapalindole U, and catalyzes
63 cycloallene C, and marilzabicycloallene D as halogenated C15-acetogenin 12-membered bicyclic and tric
64 rachlorocarbazole was one of the most active halogenated carbazoles and, like TCDD, contains 4 latera
65 (1)H NMR spectral shift data for 11 relevant halogenated carbazoles are reported, along with their ga
66 ated carbazoles, while the others were mixed halogenated carbazoles containing, in addition to bromin
67                                         Some halogenated carbazoles exhibit characteristics of persis
68  the first study discovering the seven mixed halogenated carbazoles in the environment.
69 ion is directed here to the possibility that halogenated carbazoles may currently be emitted into the
70                       The abundance of mixed halogenated carbazoles peaked at depths of 12-16 cm, rem
71 fold induction responses for the most active halogenated carbazoles was similar to that observed for
72  alkanethiols were stably immobilised on the halogenated carbon, with electrochemical chlorination be
73 ons have found that oxidative "breakers" can halogenate certain additives, but these pathways are unv
74                                              Halogenated chemical substances are used in a broad arra
75 ntially novel persistent and bioaccumulative halogenated chemicals.
76  profiles allowed the selective detection of halogenated (Cl and Br) molecules.
77 Herein, we explored the possibility of using halogenated cocaine haptens to enhance the immunological
78 togram algorithm was used to isolate unknown halogenated components using high-resolution mass spectr
79  bioinformatics tool named MeHaloCoA (Marine Halogenated Compound Analysis) was developed and include
80  was demonstrated by repetitive injection of halogenated compound into measurement solution.
81  structure proposal of a previously reported halogenated compound was revisited.
82           Decadal differences in the unknown halogenated compounds (or features) were compared with t
83 alococcoides mccartyi strains transform many halogenated compounds and are used for bioremediation.
84 rometry (HPLC-HRMS) in order to prospect for halogenated compounds and to identify potentially new on
85                           Naturally produced halogenated compounds are ubiquitous across all domains
86          A new script for the recognition of halogenated compounds based on combining a simplified is
87                  Diverse patterns of unknown halogenated compounds between lakes suggested that there
88  to mapping interaction sites using a set of halogenated compounds expressing paired hydrogen-bonding
89  demonstrate that volatilization of the four halogenated compounds from water does not cause a measur
90                 The synthesis of these inter-halogenated compounds has been enabled by our recently d
91  allowed the identification of known and new halogenated compounds in a competitive amount of time.
92 nique for the speciation analysis of organic halogenated compounds in environmental matrixes.
93            A key issue is how plants produce halogenated compounds such as 4-Cl-IAA.
94 ate binding pocket to accommodate a range of halogenated compounds that satisfy minimal structural cr
95                     The presence of multiple halogenated compounds usually poses toxicity to dehaloge
96  ratio mass spectrometry (LC-IRMS) for polar halogenated compounds was evaluated.
97 ower relative abundance of product ions from halogenated compounds was generally observed.
98                           Previously unknown halogenated compounds were detected during the analysis
99    Relative peak abundances of these unknown halogenated compounds were in the same order of magnitud
100                                       Higher halogenated compounds were not observed due to difficult
101 dicted (*)OH rate constants for 5 additional halogenated compounds within a factor of 2.
102    It initiated a renaissance of interest in halogenated compounds, and later on, when found also on
103 phenyls (PCBs) frequently coexist with other halogenated compounds, such as polybrominated diphenyl e
104 d-specific stable isotope analysis (CSIA) of halogenated compounds.
105 cal roles in environmental bioremediation of halogenated compounds.
106  at sites cocontaminated with PCBs and other halogenated compounds.
107 e capable of detoxifying a broad spectrum of halogenated compounds.
108 rylcyclopropanes under suggested nitrosating-halogenating conditions.
109 an in situ dehalogenation reaction between a halogenated conjugated diene and nitrogen-containing nuc
110                                       Legacy halogenated contaminants have been monitored in the Grea
111 here continues to be unidentified sources of halogenated contaminants in the Great Lakes missed by cu
112 he device is applicable for the detection of halogenated contaminants in water samples with pH rangin
113 cades, but there are many additional unknown halogenated contaminants potentially affecting the Great
114 or method development of LC-IRMS methods for halogenated contaminants that are known as potential thr
115 siderations and environmental remediation of halogenated contaminants.
116 defect filtering to identify bioaccumulative halogenated contaminants.
117 present a rapid and efficient synthesis of 2-halogenated cordycepins, also useful synthons for the de
118  abundant than their brominated and/or mixed halogenated counterparts.
119                             The synthesis of halogenated cyclic guanidines through iodine(III)-mediat
120 hyl)amine) complexes that can preferentially halogenate cyclohexane.
121 ctively bind methylated DNA, suggesting that halogenated cytosine damage products can potentially mim
122                            Unsymmetrically C-halogenated DBAs are formed via an electrophilic solvent
123                              Symmetrically C-halogenated DBAs are obtained through the condensation o
124                 Regardless, the reduction in halogenated DBP formation during postchloramination achi
125      O(3)/GAC was more effective at reducing halogenated DBP formation during postchloramination.
126  water led to increases in N-nitrosamine and halogenated DBP formation, suggesting the release of pre
127    Our results show the formation of complex halogenated DBPs that are formed in the treatment of wat
128                                 Unregulated, halogenated DBPs were the dominant contributors to the e
129       However, BPC promoted the formation of halogenated DBPs while a free chlorine residual was main
130                       Halofuginone (HF), the halogenated derivative of febrifugine, has been tested i
131 to the halogen free parent compounds, some 7-halogenated derivatives exhibited slightly improved inhi
132                              Analysis of the halogenated derivatives of two well-known TTR inhibitors
133 characterized by NMR spectroscopy, and their halogenated derivatives were fully characterized by NMR
134                         Brominated and mixed halogenated dibenzo-p-dioxins (PBDDs and PXDDs) may well
135 reliable and valid technique for analysis of halogenated dioxins and furans that could be used in pla
136        Here we investigated the formation of halogenated dipeptides from three aromatic dipeptides, p
137                                 To determine halogenated dipeptides in authentic water samples, we de
138 uence of CuO on the formation of BrO3(-) and halogenated disinfection byproducts (DBPs) (e.g., trihal
139 ave difficulty removing low molecular weight halogenated disinfection byproducts (DBPs) and industria
140 loramination of 35 regulated and unregulated halogenated disinfection byproducts (DBPs), 8 N-nitrosam
141 ion of bromate, 35 regulated and unregulated halogenated disinfection byproducts (DBPs), and 8 N-nitr
142 ducts (PPCPs), alkylphenols, and 21 of their halogenated disinfection byproducts.
143 es or by aqueous cross-coupling reactions of halogenated dNTPs is discussed.
144 e partially responsible for the formation of halogenated DOM, haloacetic acids, and haloacetonitriles
145 ntion toward the contribution of promiscuous halogenating enzymes in further expanding the diversity
146 rther investigate the action and activity of halogenating enzymes in plants.
147  unknown diversity of genes encoding for (de)halogenating enzymes in the soil metagenome including sp
148      The high diversity and abundance of (de)halogenating enzymes suggests a strong microbial contrib
149 er treatment plants and receiving waters and halogenated estrogens are likely produced during wastewa
150 tive mode) ionization efficiency of free and halogenated estrogens by factors of 20 and 2.6, respecti
151 ltaneously quantifying free, conjugated, and halogenated estrogens in treated wastewater effluent, in
152 ston metropolitan area, where conjugated and halogenated estrogens made up 60-70% of the steroidal es
153 urrently characterized free, conjugated, and halogenated estrogens.
154                                        The 2-halogenated ethanols activate wild-type TASK-3 with the
155 ousness associated with isoflurane, a potent halogenated ether in common clinical use.
156                   We show that both of these halogenated ethers interact with pairs of 800 nm entangl
157 ear and non-linear optical properties of the halogenated ethers sevoflurane (SEVO) and isoflurane (IS
158      The IPDC algorithm resolved 313 and 855 halogenated features in positive and negative modes, res
159                    Greater than 2000 unknown halogenated features were detected.
160 erior contained the lowest number of unknown halogenated features, whereas Lake Ontario contained the
161  legacy contaminants and a series of unknown halogenated features.
162 als to biota and do not provide the complete halogenated fingerprint of the biota.
163 hod was used to determine the presence of 65 halogenated flame retardants (HFRs) in the United Sates
164 (OCPs), 14 current use pesticides (CUPs), 47 halogenated flame retardants (HFRs), and 19 organophosph
165 brominated diphenyl ethers (PBDEs) and novel halogenated flame retardants (NHFRs) are ubiquitous, per
166 raBHD, MeO-PBDEs, Q1, and related PMBPs) and halogenated flame retardants (PBDEs, HBB, Dec 602, Dec 6
167 mpounds were detected during the analysis of halogenated flame retardants in two sediment cores colle
168                        A method to determine halogenated flame retardants was developed that utilizes
169 tant anthropogenic contaminants, such as the halogenated flame-retardants and pesticides.
170             We synthesized 700-nm and 800-nm halogenated fluorophores that show high uptake into thes
171 secticides); we then selected fludioxonil, a halogenated fungicide, as a model compound for more deta
172                             Edge-selectively halogenated graphene nanoplatelets (XGnPs, X = Cl, Br, o
173 nvolving hydrogen are still lacking for many halogenated groundwater contaminants and degradation pat
174                                            8-Halogenated guanine (haloG), a major DNA adduct formed b
175  features the formation of C-C bonds between halogenated (hetero)arenes and simple (hetero)arenes wit
176 eve the selective cross-coupling of multiply halogenated heteroarenes.
177  direct C-H arylation of nitrogen-containing halogenated heterocycles is possible without protection
178 od gives highly selective access to valuable halogenated heterocycles with regiochemistry complementa
179 an be very facile and are effective means of halogenating heterocycles.
180 nitrated and halogenated aromatic compounds, halogenated heterocyclic aromatic compounds, and halogen
181                                              Halogenated homo- and heterocyclic aromatics including d
182 e of PXDD/Fs from dihalogenated through hexa-halogenated homologue groups.
183 in film sensors using Fujiwara reactions for halogenated hydrocarbon detection.
184            During the physical adsorption of halogenated hydrocarbon vapours, such as dibromomethane,
185  one of the only known methods for detecting halogenated hydrocarbons in the visible spectrum.
186 onitrile)), and undisclosed compounds (e.g., halogenated hydrocarbons, such as 2-bromohexane or 4-bro
187 romatic hydrocarbons, siloxanes, and certain halogenated hydrocarbons.
188                             A variety of C-3 halogenated imidazo[1,2- a]pyridines and benzo[d]imidazo
189 yclization reaction of aryldiynes to produce halogenated indeno[1,2-c]chromene derivatives is describ
190 of Na+ and K+ channels strongly suggest that halogenated inhalational general anesthetics interact wi
191                                              Halogenated inhaled general anesthetic agents modulate v
192                                              Halogenated ions were assigned in four DBP elemental gro
193 ipt is based on the recognition of a generic halogenated isotope cluster pattern that allows for the
194 agents with N-heterocyclic halides, aromatic halogenated ketones or imines, and alkenyl iodides.
195                                              Halogenated l- or d-tryptophan obtained by biocatalytic
196                                   Twenty-one halogenated legacy and current-use pesticides and pestic
197 this article, we investigated the ability of halogenated ligands to modulate the self-assembly of amy
198 aining either halogenated building blocks or halogenated ligands.
199                                              Halogenated membranes were characterized after treatment
200 e polycycles merochlorin A and B are complex halogenated meroterpenoid natural products with signific
201           In contrast, the identification of halogenated methanes and acetones suggested that those c
202 oral hydrate), to ethanol, and to a panel of halogenated methanes and alcohols.
203 ehalobacter strains in the transformation of halogenated methanes.
204 ethod is robust for a wide range of nonpolar halogenated micropollutants in all matrices.
205 thod to detect and quantify diverse nonpolar halogenated micropollutants in wastewater treatment plan
206                                              Halogenated molecular formulas were identified and confi
207         After DICD treatment, a total of 213 halogenated molecular ions with relative abundance of at
208 halogenases are useful enzymes for providing halogenated molecules with improved biological activity,
209 n reactions provide efficient access to many halogenated molecules, the use of typical protocols for
210 windmill" pattern of bonding among the fully halogenated molecules.
211 oped procedure results in extremely valuable halogenated N-arylcarbmates that can further be hydrolyz
212                                 Thousands of halogenated natural products (HNPs) pervade the terrestr
213                                              Halogenated natural products (MHC-1, TriBHD, TetraBHD, M
214                                        Plant halogenated natural products are rare and harbor various
215                                              Halogenated natural products constitute diverse and prom
216 ntermediates in the biosynthesis of numerous halogenated natural products from Laurencia species.
217                   At last count, nearly 5000 halogenated natural products have been discovered.
218 enzymes, responsible for the biosynthesis of halogenated natural products, as biocatalysts.
219 s technology that would aid the synthesis of halogenated natural products, as well as existing method
220                                      Six new halogenated natural products, breitfussin C-H (3 - 8) we
221 able screening of a large number of reported halogenated natural products, resulting in expedient str
222 cetogenins is Nature's largest collection of halogenated natural products, with many of its members p
223 this is the first time that the formation of halogenated nitrogenous heterocyclic compounds is report
224  A vast majority of the X-bonds is formed by halogenated nucleobases, such as bromouridine, and featu
225 ough aqueous Suzuki-Miyaura crosscoupling of halogenated nucleosides or nucleotides with 4-(trifluoro
226                                              Halogenated o-methylbenzene, dimethoxybenzene, and thiop
227                                However, many halogenated oligocyclic aromatic compounds occur in natu
228 on of these emerging solvents, in particular halogenated ones, but also at providing a medium term pe
229                            Concentrations of halogenated OPEs seemed to be driven by river discharge
230                Chloroform is an example of a halogenated organic compound with natural formation as i
231                                      We used halogenated organic compounds (HOC), a chemical class th
232    To catalog the diversity and abundance of halogenated organic compounds (HOCs) accumulating in hig
233                              This library of halogenated organic compounds (HOCs) consisted of 180 an
234 Lake Ontario had the largest number of novel halogenated organic compounds (NHOCs).
235                                     Volatile halogenated organic compounds (VOX) contribute to ozone
236 t Lakes to characterize a more robust set of halogenated organic compounds across species and among l
237                                              Halogenated organic compounds are also common intermedia
238                          The high utility of halogenated organic compounds has prompted the developme
239                             The abundance of halogenated organic compounds in flowback fluids rather
240 ng recognition of the occurrence of natural, halogenated organic compounds in marine and terrestrial
241                 Electrochemical reduction of halogenated organic compounds is gaining increasing atte
242 f organic compounds (e.g., carbon disulfide, halogenated organic compounds).
243                                              Halogenated organic compounds, also termed organohalogen
244                               The identified halogenated organic compounds, particularly iodinated or
245 ia Bight (SCB) are exposed to high levels of halogenated organic contaminants (HOCs), which have prev
246 ) operations reveal consistent detections of halogenated organic species , yet the source of these co
247 further investigation into the occurrence of halogenated peptides in other drinking water systems.
248                                    Seven new halogenated peptides termed svetamycins A-G (1-7) have b
249 s for future studies on remediation of other halogenated persistent aromatic pollutants by advanced o
250                                              Halogenated phenazine 14 proved to be the most potent bi
251 ucture-activity relationships of a series of halogenated phenazines (HP) inspired by 2-bromo-1-hydrox
252                        We report a series of halogenated phenazines (HP), inspired by marine antibiot
253 e first modular synthesis of a library of 20 halogenated phenazines (HP), utilizing the Wohl-Aue reac
254                                              Halogenated phenolic compounds (HPCs) including hydroxyl
255 yzed mussel samples after methylation of the halogenated phenolic compounds (HPCs).
256 ding polybrominated diphenyl ethers (PBDEs), halogenated phenols and bisphenols, and their metabolite
257 164 persistent organic pollutants (POPs) and halogenated phenols in 53 Hawaiian green turtle (Cheloni
258                              The presence of halogenated phenols in sea turtles is a novel discovery;
259               Four classes of POPs and seven halogenated phenols were detected in at least one of the
260 ctively as a peroxidase on the full range of halogenated phenols.
261 rahydropyridazine-3-carboxylic acid, a gamma-halogenated piperazic acid, and a novel delta-methylated
262 trochemical studies of various categories of halogenated pollutants (chlorofluorocarbons; disinfectio
263 plied for the detection of several important halogenated pollutants under laboratory conditions, e.g.
264                    The majority of these are halogenated polycyclic aromatic hydrocarbons (halo-PAHs)
265 ontaining formulas suggested the presence of halogenated polyphenolic and aromatic acid-type structur
266 mmetrically functionalized BODIPYs involving halogenated positions) can now be made.
267                                          The halogenated products obtained in this reaction are highl
268                                          The halogenated products were deoxygenated by PCl3 or PBr3.
269 -H bond, which results in good yields of the halogenated products with excellent regioselectivity.
270 xidation capacity of PDS and producing toxic halogenated products.
271 coupling aryl or alkyl Grignard reagents and halogenated purine nucleosides in the presence of Fe(aca
272 tal complexes, but strategies to selectively halogenate pyridine C-H precursors are lacking.
273 ocontrol, where single-electron reduction of halogenated pyridines regiospecifically yields the corre
274                                              Halogenated pyrroles (halopyrroles) are common chemical
275 dichloromethyl)-5-hydroxy-2(5H)-furanone) or halogenated pyrroles.
276                                     RSEs for halogenated rings rise significantly from 8-9 kcal mol(-
277                               Closantel is a halogenated salicylanilide with a potent anti parasitic
278 t simple liquid electrolytes reinforced with halogenated salt blends exhibit stable long-term cycling
279  is similar to the percentage of misassigned halogenated sesquiterpenes reported previously.
280 loSeeker's ability to filter and investigate halogenated signals was demonstrated and illustrated by
281             A global strategy aiming to seek halogenated signatures in full-scan high-resolution mass
282 rescence quenching response, and low cost of halogenated solvent composites, the sensor system presen
283 phenyl (DPI-BP), which can be dissolved into halogenated solvents (e.g., CHCl3, CH2Cl2) to enable ins
284         When exposed to gamma radiation, the halogenated solvents decompose into various radicals, in
285 ly thick BHJ layer and processed through non-halogenated solvents, indicating these high-performance
286   Pristine DPI-BP is strongly fluorescent in halogenated solvents.
287                            The coemission of halogenated species has also been speculated to have led
288 ctivated by a multiple agents and requires a halogenated substituent between approximately 30 and 232
289 ery similar dinitrobenzene isomers and three halogenated, substituted benzene compounds.
290 he most electron-rich position of the (multi)halogenated substrates, complementing established method
291 achieve this, we devise a synthetic route to halogenated sulfonated carbofluoresceins from readily av
292               A new convenient and versatile halogenating system (R(4)NHal/NOHSO(4)), giving straight
293 aper, we examine more than 100 structures of halogenated terpenoids and other natural products with t
294 e sulfoxide and the amide functional groups, halogenating the phenyl rings, and/or functionalizing th
295 ogenated, which is evident from the ratio of halogenated to nonhalogenated species.
296                                        Other halogenated trace gases were also measured, and there we
297                                              Halogenated triarylboranes (BAr(3)) have been known for
298 ophenyl)borane [B(C(6)F(5))(3)] to the other halogenated triarylboranes, to give a greater breadth of
299 sthetics, recent studies suggest that modern halogenated volatile anesthetics induce potent anti-infl
300                   Salicylic acid was readily halogenated, which is evident from the ratio of halogena

 
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