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1 2H-5,10,15,20-Tetrakis-(3,5-di-tert-butyl)-phenylporphyr
4 e-catalyzed amination of 4-bromophthalazin-1(2H)-ones 4 with primary amines generates aminophthalazin
5 tetrahydroxy-6-methyl-3,4-dihydroanthracen-1(2H)-one (up to 82% for AflM) has also been observed in p
6 3,5-trifluoro-4-(4-oxo-3,4-dihydropyridin -1(2H)-yl)phenyl)oxazolidin-2-one (MRX-I), distinguished by
7 henyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acet amide (PF-06282999, 8) upon oral administrat
8 1H-inden-1-one (3), 3,4-dihydro-naphthalen-1(2H)-one (4), and cycloalkanones (5-7) were studied for t
9 t regioselective bromination of phthalazin-1(2H)-ones 3 with benzyltrimethylammonium tribromide (BTMA
11 onate ([Cp*Rh(MeCN)3](SbF6)2) reacts with 1-(2H)-phthalazinones to promote a C-H functionalization ev
12 9-def :6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone) (PNPDI); and poly(9,9-bis(2-butyloctyl)
16 ntification of [Ru(eta(6)-p-cymene)Cl2(1H,1H,2H,2H-perfluorodecyl-3-(pyridin-3-yl)propanoate)], a rut
17 2H-perfluorooctyl) trichlorosilane or (1H,1H,2H,2H-perfluorooctyl) dimethylchlorosilane to a specific
18 By controlling the contact angle of (1H,1H,2H,2H-perfluorooctyl) trichlorosilane or (1H,1H,2H,2H-pe
19 ips were functionalized with trichloro(1H,1H,2H,2H-perfluorooctyl)silane on one side, to render the s
20 the FET performance, suggesting that the 1T/2H interface controls carrier injection into the channel
25 (+) dioxygen-reduction (to water) to a 2e(-)/2H(+) process (to hydrogen peroxide) only by increasing
27 to 2-(1,3-dihydroxyallylidene)-1H-indene-1,3(2H)-dione or by loss of alcohol to indeno[1,2-b]pyran-4,
29 ve compound, 2-phenyl-1,2-benzisoselenazol-3(2H)-one (ebselen), displayed Ki values equal to 2.11 and
30 ion of 7-nitro-2-aryl-1,2-benzisoselenazol-3(2H)-ones 3 and 6 with sodium benzenetellurolate, NaTeC6H
34 F-7-carboxamide) and 2,3-dihydrobenzofuran-3(2H)-one-7-carboxamide (DHBF-3-one-7-carboxamide) derivat
35 ene affords the corresponding dihydrofuran-3(2H)-ones in excellent yields via a formal 5-endo-trig cy
36 ng, amongst others, 4-hydroxy-2,5-dimethyl-3(2H)-furanone (furaneol), vanillin, (E)-4,5-epoxy-(E)-2-d
37 oil roasted almonds 4-hydroxy-2,5-dimethyl-3(2H)-furanone, 2,3-pentanedione, methional and 2-acetyl-1
38 the biosynthesis of 4-hydroxy-2,5-dimethyl-3(2H)-furanone, a major component in the characteristic fl
39 overall aroma were 4-hydroxy-2,5-dimethyl-3(2H)-furanone, methyl benzoate, (E)-2-hexenal, and hexana
42 one (6-(4-fluorophenyl)-4-hydroxypyridazin-3(2H)-one) also retained modest activity as an inhibitor.
43 Several varied 6-phenyl-4-hydroxypyridazin-3(2H)-ones and 2-phenyl-5-hydroxypyrimidin-4(3H)-ones were
45 ave identified 2-phenyl benzo[d]isothiazol-3(2H)-ones as species-selective inhibitors of Plasmodium s
48 p henyl)amino)-1H-pyrazolo[3,4-d]pyrimidin-3(2H)-one] using simultaneous and sequential dosing schedu
49 carbanion reagent studies suggest that the 3(2H)-furanone is formed in a cascade of reactions involvi
51 ylene] amino}spiro[isoindole-1,9'-xanthen]-3(2H)-one (DEMAX) for Al(III) chelation is described herei
52 gies, derivatives of 4, 4'-bis(5-nitro-1,2,3-2H-triazole) were designed, synthesized, and characteriz
53 perfluorophenyl; 3d, heptafluoropropyl; 3e, 2H-pyrroliumyl) were synthesized in two or three steps f
54 2-(naphthalen-1-ylmethyl)-1,2,4-triazine-3,5(2H,4H)-dione 11h was found to be selective over a number
55 f 2-substituted 6-hydroxy-1,2,4-triazine-3,5(2H,4H)-dione derivatives were synthesized as inhibitors
58 8-fluoro-3,4-dihydro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetic acid (1, Setipiprant/ACT-129968) were synt
59 -fluoro-3,4-dihyd ro-1H-pyrido[4,3-b]indol-5(2H)-yl)acetic acid, respectively, each composed of two e
60 The synthesis of 3,4-dihydro-1,2-oxazepin-5(2H)-ones and 2,3-dihydropyridin-4(1H)-ones from beta-sub
62 copper nanocluster, [Cu20H11{Se2P(OiPr)2}9] (2H), which exhibits an intrinsically chiral inorganic co
65 aldehydes and 2-bromoallyl sulfones afforded 2H- and 4H-chromenol derivatives endowed with a 3-arylsu
66 of substituted, functionalized alpha-alkoxy 2H-naphthalenones from readily available N-tosylhydrazon
67 c route provides practical access to 2-alkyl-2H-indazol-3-yl benzoates and 2-alkyl-1,2-dihydro-3H-ind
71 rogen bond between the carboxylate group and 2H of the quinolinium ring, in addition to a 1,5-interac
73 yl-lithium are a mixture of 1T (primary) and 2H (secondary) phases and oxidize rapidly with a typical
74 nitrogen leading to the synthesis of 2-aryl-2H-benzotriazoles has been accomplished with the help of
75 ithioates and alkyl 3,4-dihydro-2-oxo-4-aryl-2H-chromen-3-ylcarbamodithioates from 2-(alkylthio)thioa
76 rgent, one-step benchtop syntheses of N-aryl-2H-indazoles and furans by C-H bond additions to aldehyd
78 f diastereomeric 2-silyl-5,6-dihydro-6-aryl-(2H)-pyrans via [1,2]- and [1,4]-Wittig rearrangements to
79 homojunctions have abrupt interfaces between 2H and 1T' MoTe2 domains, possessing a potential differe
81 atalytic site chemistry was slowed for both [2H]PNP and [13C, 15N]PNP in proportion to their altered
83 mportant electronic band parameters for bulk 2H-MX2, including the band gap, direct band gap size at
85 hexagonal dislocation spirals form the bulk 2H layer stacking commonly observed, and plates containi
87 ar copolymer chains containing phenyl-Si(CH3)2H pendants were the major product for both DMSS comonom
89 lling microscopy, the canonical CDW compound 2H-NbSe2 intercalated with Mn and Co, and show that the
94 itrile-functionalized porphyrin derivatives (2H-TPCN) with Co atoms in an ultrahigh vacuum environmen
95 for the preparation of allylic amide derived 2H-chromenes using an Overman rearrangement and a 6-endo
97 droxymethyl-4-piperidyl]-3-ethyl-1,3-dihydro-2H benzimidazol-2-one] and the DOP receptor agonist SNC-
98 ymethyl)-4-piperidinyl]-3-ethyl -1,3-dihydro-2H-benzimidazol-2-one] to explore structure-activity rel
99 nthesis of highly functionalized 1,3-dihydro-2H-benzimidazol-2-ones via a ring opening of thiazolo[3,
100 scopy demonstrates that 1-methyl-1,3-dihydro-2H-benzimidazole-2-selone, H(sebenzim(Me)), a structural
101 = 1,3-bis[2,6-diisopropylphenyl]-1,3-dihydro-2H-imidazol-2-ylidene) provided only the alkene hydroary
102 ylphenyl)piperazine-1-yl]butyl}p-1,3-dihydro-2H-indol-2-one) and Cimbi-717 (3-{4-[4-(3-methoxyphenyl)
103 oxyphenyl)piperazine-1-yl]butyl}-1,3-dihydro-2H-indol-2-one) as selective 5-HT7R PET radioligands in
104 tory activity, and (4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N'-[(4-ethoxyphenyl)methylidene]benzo
106 d for 7-chloro-4-(2-fluoroethyl)-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide (BPAM121) at the h
109 cyclopropyl-7-(3-methoxyphenoxy)-3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxide, EC50 = 2.0 nM).
110 nthesis of 7-phenoxy-substituted 3,4-dihydro-2H-1,2,4-benzothiadiazine 1,1-dioxides and their evaluat
111 of (S)-(-)-7,8-difluoro-3-methyl-3,4-dihydro-2H-benzo-[b][1,4]oxazine, which is a key precursor of th
112 sis of a wide family of 3-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazines bearing different pattern subst
113 a new class of 2-benzyl-3-phenyl-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazines has been discovered durin
115 eceptor antagonist JNJ16259685 ((3,4-Dihydro-2H-pyrano[2,3-b]quinolin-7-yl)-(cis-4-methoxycyclohexyl)
118 ts in the pairwise generation of 3,4-dihydro-2H-pyrrole and an allylruthenium complex, which combine
122 thermore, oxidative couplings of 3,4-dihydro-2H-pyrrole-2-carbonitriles with copper(II)-salts furnish
123 s developed, employing 4-methoxy-1,5-dihydro-2H-pyrrol-2-one (13) as a single starting material to pr
124 cid (2) and 3-((5-butyl-3-methyl-5,6-dihydro-2H-pyran-2-yl)-methyl)-4-methoxy-4-oxobutyl benzoate (3)
125 rs in cis- and trans-substituted 3,6-dihydro-2H-pyrans allows the relative configuration at the C3 an
126 ration of 4,5-bis(organoselanyl)-3,6-dihydro-2H-pyrans and to 4-amino-butynol for the preparation of
127 udied using 5-bis(organoselanyl)-3,6-dihydro-2H-pyrans as substrate in a Kumada-type cross-coupling r
128 ive coupling reactions furnished 3,6-dihydro-2H-pyrans through a chemo- and regioselective 6-endo cyc
129 tion of 2,5-dihydro-1H-pyrroles, 3,6-dihydro-2H-pyrans, and pyrroles has been achieved through switch
133 -2-ones 15-20, 8,9-disubstituted-3,9-dihydro-2H-purin-2,6-diamines 21-24 and 6-imino-1-phenyl-8,9-dis
134 9-14, 6-amino-8,9-disubstituted-3,9-dihydro-2H-purin-2-ones 15-20, 8,9-disubstituted-3,9-dihydro-2H-
136 nes, resulting from reaction of 2,3-diphenyl-2H-azirine and diazo compounds, do not produce indoles v
139 rence of different reaction paths of double (2H(+)/2e(-)) free radical scavenging mechanisms was esti
142 is generates a new FeMo-co state, denoted E4(2H)*, through the photoinduced re of the two bridging hy
143 ryoannealing at temperatures above 175 K, E4(2H)* reverts to E4(4H) through the oxidative addition (o
145 oyloxy)-ethyl)-hexahydro-4-((E)-pent-2-enyl)-2H-chromene-6-carboxylate of polyketide origin, with act
146 A series of N(6)-substituted-5'-C-(2-ethyl-2H-tetrazol-5-yl)-adenosine and 2-chloro-adenosine deriv
148 in downregulated PTEN protein levels (Figure 2H), downregulation of both mRNAs (Figure 2G), and incre
151 H substitution for F on the alpha carbon for 2H polyfluorocarboxylic acids (2HPFCAs) and (ii) bearing
152 and a lowering of DeltaG(H) from +1.6 eV for 2H to +0.18 eV for 1T', comparable to 2H molybdenum disu
153 elds catalytic exchange rates (at the formal 2H(+)/H2 potential, at 0 degrees C) of 157 electrons (78
155 mately 50 mV per decade can be achieved from 2H-phase catalysts where only the basal plane is exposed
156 ional analysis of the C-C bond cleavage from 2H(+) gives an intrinsic CKIE of 1.051 and suggests two
158 4-triazol-4-ium bromides, were prepared from 2H-azirines and triazolium phenacyl bromides using a sim
161 (11)C]-(+)-4-propyl-3,4,4a,5,6,10b-hexahydro-2H-naphtho[1,2-b][1,4]oxazin-9-ol) to test the hypothesi
162 pp}2C5H3N (II) (hppH = 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine) were protonated using [HNE
163 red the role of hppH [=1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine] to act not only as a base
164 omer yields the parent 4,5,6,7,8,9-hexahydro-2H-cyclooctatriazole, which could be characterized as a
165 d acids, the reaction provides the hexahydro-2H-thieno[3,2-c]pyran skeleton predominantly via oxonium
166 wis or Bronsted acids provides the hexahydro-2H-thiopyrano[4,3-b]furan preferentially through thioniu
167 tion to afford well-characterized hydrides ([2H](+) and [3H](+)) and mixed-valence derivatives ([2](+
168 he synthetically important lactol, 6-hydroxy-2H-pyran-3(6H)-one (3), proceeds cleanly in the presence
169 o be 2-amino-4-(2-hydroxy-3-(2-hydroxyethyl)-2H-benzo[b][1,4]oxazin-5-yl)-4-oxobutanoi c acid, which
170 t the Zeeman splitting, however, persists in 2H-MoTe2 bilayers, as a result of an additional degree o
172 a constant drive the moving vortex state in 2H-NbS2 superconductor exhibits a negative differential
174 lective catalytic synthesis of 2H-indazoles, 2H-benzotriazoles, and related fused heterocyclic system
175 rgy demanding than the first ones indicating 2H(+)/2e(-) processes as inherent to catechol moiety.
177 hylsilyl)aryl triflates smoothly insert into 2H-azirines to form 2,3-diarylindoles with high selectiv
178 tion to ammonia is enabled by intramolecular 2H(+)/2e(-) proton-coupled electron transfer from the sa
180 guided isolation of 3-(octahydro-9-isopropyl-2H-benzo[h]chromen-4-yl)-2-methylpropyl benzoate and met
182 t exciton resonance A and B of the few layer 2H-MoS2 affecting optical absorption and subsequent mech
185 sile strains to the semiconducting few-layer 2H-MoS2 crystals in the nanocomposite resulted in spatia
189 of the stoichiometric reaction between [(LCu)2H](+) and CO2 is dramatically increased in the presence
192 gnificantly enhanced CO2 reactivity of [(LCu)2H](+) under these catalytically relevant conditions, LC
194 e addition of a large excess of DBU to [(LCu)2H](+) results in an equilibrium that forms LCu(DBU)(+)
198 al isomers (AT-hook peptide 3 KRGRGRPRK [M + 2H](+2)), and a complex mixture of polyaromatic hydrocar
201 ionized preferentially as the dianion ([M - 2H](2-)) with a small contribution of the monoanion ([M
202 Product ion spectra generated from the [M - 2H](2-) precursor ions were dominated by the loss of HSO
205 yloxy)-10-methylpentyl)-tetrahydro-13-methyl-2H-pyran-17-car boxylate (2) and (13-(methoxycarbonyl)-1
206 43654 [(2S)-1-(1H-indol-3-yl)-3-[5-(3-methyl-2H-indazol-5-yl)pyridin-3-yl]oxypropan-2-a mine; ATP-com
207 S)-6-(2,9-dihydroxynonyl)-4-hydroxy-3-methyl-2H-pyran-2-one, 4-hydroxy-3-methyl-6-((2S,4R)-2,4,11-tri
209 yl-(1H)-tetrazole-5-amine (1a) and 2-methyl-(2H)-tetrazole-5-amine (1b), although resulting in a comm
210 S6180 (4-[[3-(trifluoromethyl)phenyl]methyl]-2H-1,4-benzothiazin-3(4H)-one) inhibition at the atomist
211 optimization of the basal plane of monolayer 2H-MoS2 for HER by introducing sulphur (S) vacancies and
212 ineered low-resistance contacts on monolayer 2H-phase MoS2 basal plane lead to higher efficiency of c
213 A novel phase transition, from multilayered 2H-MoTe2 to a parallel bundle of sub-nanometer-diameter
214 Our efforts have led to compound 1, N-((2H-tetrazol-5-yl)methyl)-4-((R)-1-((5r,8R)-8-(tert-butyl
216 thoxy-4-2-[(4-methylpentyl)oxy]-3,4-dihydr o-2H-6-pyranylbutanoic acid (2) and 3-((5-butyl-3-methyl-5
217 dehydes provides the corresponding octahydro-2H-cyclopenta[c]furo[2,3-d]pyran derivatives in good yie
218 Ruthenium-catalyzed oxidative annulation of 2H-chromene-3-carboxamides with alkynes has been achieve
220 icient Pd-catalyzed C-H functionalization of 2H-indazole at C3-position via an isocyanide insertion s
222 (S)-vacancies created on the basal plane of 2H-molybdenum disulfide (MoS2) using argon plasma exposu
223 ting patterns in multinuclear NMR spectra of 2H indicate that the chiral Cu20H11 core retains its C3
224 of these intermediates for the synthesis of 2H-1,4-oxazine N-oxides has been developed for a variety
225 scope of the new method for the synthesis of 2H-1,4-oxazine N-oxides is discussed, in addition to ini
226 ides a chemoselective catalytic synthesis of 2H-indazoles, 2H-benzotriazoles, and related fused heter
228 Al composites reinforced with either IF- or 2H-WS2 particles, so as to elucidate their mechanism of
230 dro-16-hydroxy-15-(methyl pentanoate)-14-oxo-2H-pyran-13-yl)-9-methyl-but-11-enyl benzoate (1), isobu
232 stituted phenylacetones to substituted 2-oxo-2H-pyran-3-carbonitriles at room temperature under alkal
235 In contrast, photolysis of 2-methyl-3-phenyl-2H-azirine (1b) in acetonitrile yields heterocycles 6 an
236 scover modified salicylanilides and 3-phenyl-2H-benzo[e][1,3]oxazine-2,4(3H)-dione derivatives as pot
237 oic acid, HAvo; and 4-(2,2-difluoro-6-phenyl-2H-1lambda(3),3,2lambda(4)-dioxaborinin-4-yl)benzoic aci
238 06 (8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H-[1,2,4]triazolo[3,4-f][1,6]naphthyri din-3-one;dihydr
242 copy and Raman mapping confirm that in-plane 2H-1T' MoTe2 homojunctions have abrupt interfaces betwee
243 2) or [2,6-((i)Pr2PO)2-4-(MeO)C6H2]Fe(PMe2Ph)2H (3) have been tested for catalytic dehydrogenation of
244 the formula of [2,6-((i)Pr2PO)2C6H3]Fe(PMe2R)2H (R = Me, 1; R = Ph, 2) or [2,6-((i)Pr2PO)2-4-(MeO)C6H
246 ural transformation from trigonal prismatic (2H) to octahedral (1T) upon lithium or sodium intercalat
249 cle N(2) arylation in 1-beta-d-ribofuranosyl-2H-1,2,3-triazole substrate were designed in this study.
250 m dioxygenation of pyrene at an apical ring, 2H-naphtho[2,1,8-def]chromen-2-one (NCO), which was conf
251 lap near the Fermi level, but semiconducting 2H-MoTe2 is more stable and therefore more accessible sy
254 ever, metals deposited on the semiconducting 2H phase usually form high-resistance (0.7 kOmega mum-10
257 ms exhibit a well-defined crystal structure (2H phase) and large grains reaching several hundred micr
259 nedicarboxylate to access highly substituted 2H-furo[2,3-c]pyrrole bearing two rings and four stereoc
260 e and furnishes a wide range of 2-substiuted 2H-thiochromenes with excellent enantioselectivities (up
261 a higher-energy protonated phenyl tautomer (2H(+)) prior to C-C bond breaking would produce protonat
262 ructural data for [Cp(C5F4N)FeH(P(tBu)2N(tBu)2H)](+) provide a glimpse of how the H-H bond is oxidize
263 group A rotavirus VP3 contains a C-terminal 2H-phosphodiesterase domain that can cleave 2'-5' oligoa
264 7 (3-[(3-Chlorophenoxy)methyl]-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrim idin-4-amine hydr
265 ymethyl)-3-pyridinyl]-4-{[(1R)-1-(tetrahydro-2H-pyran-4-yl)ethyl]amin o}-3-quinolinecarboxamide (72)
266 of cis- and trans-fused 3,4,4a,8a-tetrahydro-2H,5H-pyrano[2,3-b]pyran-7-carboxylates have been obtain
268 ctions produced diverse 1,3a,4,9b-tetrahydro-2H-furo[2,3-c]chromene-2,7-diols and 3,4,4a,9a-tetrahydr
269 ed 1,4-oxazines (morpholines) and tetrahydro-2H-1,4-thiazines (thiomorpholines), and seven-membered 1
270 azine (6) obtained from 4,4',5,5'-tetranitro-2H,2'H-3,3'-bipyrazole (4) by N-amination and N-azo coup
279 r 1b points to the possibility that only the 2H-tetrazoles forms can give a direct access to nitrile
281 sible electrocatalytic behavior close to the 2H(+)/H2 potential, making them paradigms for efficiency
284 tion of thiazolo-, thiazino-, and thiazepino-2H-indazoles from o-nitrobenzaldehydes or o-nitrobenzyl
286 e derived from acyclic 2-oxo-butanoate 10 to 2H-azirine phosphine oxide 1 led to vinylogous N-acyl-al
287 ates derived from indenone-carboxylate 15 to 2H-azirines 1 led to the formation of functionalized N-s
288 eV for 2H to +0.18 eV for 1T', comparable to 2H molybdenum disulfide edges on Au(111), one of the mos
289 somerization, transformation of isoxazole to 2H-azirine, which is compatible with Ph3PAuNTf2, catalyz
290 entially alters the yields of 2,2,4-triamino-2H-oxal-5-one (Z) and 8-oxo-7,8-dihydro-2'-deoxyguanosin
291 -methyl-6-((2S,4R)-2,4,11-trihydroxyundecyl)-2H-pyran-2-one, and its unnatural 2R,4R-isomer starting
292 l recessive Charcot-Marie-Tooth disease type 2H on chromosome 8q13-21.1 was excluded by linkage analy
293 easuring the conversion of hyperpolarized [U-2H, U-13C]glucose to lactate using 13C magnetic resonanc
296 nalyzed using in vivo 13C/31P/1H and ex vivo 2H magnetic resonance spectroscopy before and during hyp
297 ent highly selective reaction of arynes with 2H-azirines allowing the synthesis of either N-unsubstit
298 d reactions of diazo carbonyl compounds with 2H-azirines, dramatically depend on the nature of substi
299 roxy-2,8-dimethyl-6-(3-methyl-2-bute n-1-yl)-2H-1-benzopyran-4,7(3H,8H)-dione; 3-[(2-O-beta-d-glucopy
300 occurring sibirinone, (E)-6-(pent-1-en-1-yl)-2H-pyran-2-one, and (E)-6-(hept-1-en-1-yl)-2H-pyran-2-on
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