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1 enediamine, 1,2-pn; isobutylenediamine, ibn; trans-(+/-)-1,2-diaminocyclohexane, dach; 1,3-propylened
2  A healthy man was given an oral dose of all-trans [10,10',11,11'-(14)C]-beta-carotene (1.01 nmol; 10
3    Following photoaffinity labeling with all-trans-[11,12-(3)H]retinoic acid, the most abundant label
4                        Automerization in tri-trans-[12]annulene (1) was investigated by DFT, MP2, and
5 anar, bond-equalized radical anion of 1,7-di-trans-[12]annulene (4a(*-)) is lowest in energy; several
6 l anion, [16]annulene radical anion, and tri-trans-[12]annulene radical anion indicate that electron
7 to a highly twisted structure for the 1,7-di-trans-[12]annulene radical anion.
8 the formation of the anion radical of 1,5-di-trans-[12]annulene, which loses hydrogen and undergoes r
9 o yield two isomers of [12]annulyne (3,11-di-trans-[12]annulyne and 5,9-di-trans-[12]annulyne), both
10                       A third isomer (3,9-di-trans-[12]annulyne) was generated via the complete dehyd
11 ulyne (3,11-di-trans-[12]annulyne and 5,9-di-trans-[12]annulyne), both of which exhibit a weak paratr
12 -(+)-MR200], cis-(-)-1a [cis-(-)-MR201], and trans-(+/-)-1a [trans-(+/-)-MR204], have been identified
13 hese data clearly demonstrated that compound trans-(+)-1d, due to its sigma1 agonist activity and fav
14         An in vivo evaluation evidenced that trans-(+)-1d, in contrast to trans-(-)-1d, cis-(+)-1d, o
15                 The most promising compound, trans-(+)-1d, showed remarkable selectivity over a panel
16  evidenced that trans-(+)-1d, in contrast to trans-(-)-1d, cis-(+)-1d, or cis-(-)-1d, which behave as
17  to 1-carboxy-2-aryl-cyclopropanes with high trans-(1R,2R) selectivity and catalytic activity.
18 DPE (100 nmol), but not by the kappa agonist trans-(1S,2S)-3,4-dichloro-N-mathyl-N-[2-(1-pyrrolidinyl
19 propanation biocatalysts complements that of trans-(1S,2S)-selective variants developed here and prev
20                    The metabotropic agonist, trans-(1S,3R)-1-amino-1,3-cyclopentanedicarboxylic acid
21                              (+)-2-Cyano-1-{[trans-(1S,3S)-3-(1H-imidazol-4-yl)cyclopentyl]methyl}-3-
22 opropane-1-carboxylic acid], and trans-DCCA [trans-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-car
23 .68%), d-allose (3.67%) and 5-Caranol, trans,trans-(+)- (2.14%) were identified from Halodule pinifol
24 MAPA are mostly close to statistical (gauche/trans = 2/1) in other protic solvents, e.g., alcohols.
25 ioavailability of cis (24.5% +/- 6%) and all-trans (23.2% +/- 8%) isomers did not differ, endogenous
26       We have located six minima: two doubly trans (26, 27), one triply trans (28), one singly trans
27 inima: two doubly trans (26, 27), one triply trans (28), one singly trans (29), one quintuply trans (
28  (26, 27), one triply trans (28), one singly trans (29), one quintuply trans (trannulene-type, 33), a
29  synthesis of a C-activated N-Fmoc-protected trans-(2S,3S)-3-aminotetrahydrofuran-2-carboxylic acid a
30 it 2, resulting in identification of racemic-trans-(3-((4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-
31 received an intraperitoneal injection of all-trans ((3)H)retinol.
32 (DAMGO), [D-Ala2,D-Leu5]-enkephalin (DADLE), trans-(+/-)-3,4-dichloro-N-methyl-N-(2-[1-pyrrolidinyl]c
33 H-3-benzaze pine hydrochloride) and U50488H (trans-(+/-)-3,4-dichloro-N-methyl-N-[2-(pyrrolidinyl)cyc
34                            Incubation of all-trans [(3)H]-retinyl palmitate with RPE microsomes gener
35 y for cyano(6-methoxy-naphthalen-2-yl)methyl trans-[(3-phenyloxiran-2-yl)methyl] carbonate.
36                        The conversion of all-trans-[3H]retinol to 11-cis-[3H]retinol was used as the
37 ectric field showed a significant release of trans-(4.01+/-0.48) and cis-(5.04+/-0.26mug/g) lycopene,
38  enriched not naturally occurring isomers of trans-(-)-(4R,5S)-4b or cis-(+)-(4R,5R)-4a were formed p
39 idiella resinae KCH50 afforded a mixtures of trans-(+)-(4S,5R)-4b with enantiomeric excess ee=99% and
40                                              Trans-(+)-(4S,5R)-isomer (ee=99%) of whisky lactone 4b w
41 egioselectively at the 15-position to give a trans-(5,15)-AB-bacteriochlorin building block.
42 y established by X-ray analysis of precursor trans-(+)-5a as camphorsulfonyl derivative 9.
43 esion exists as a mixture of cis-(5R,6S) and trans-(5R,6R) epimers; these modulate base excision repa
44               We examine the 7:3 cis-(5R,6S):trans-(5R,6R) mixture of epimers paired opposite adenine
45 hat over three-quarters of these eQTL act in trans (78%) and that 86% of these differentially regulat
46 3.1.0(2,7)]dodecane moiety having either the trans (8a-e) or cis (9a-e) relative configuration of the
47 w specificity: many aldehydes, including all-trans-, 9-cis-, 11-cis-, and 13-cis-retinals and even be
48 ,O = kappa2-O,O-acetylacetonate, -Ir- is the trans-(acac-O,O)2Ir(III) motif, R = CH3, C2H5, Ph, PhCH2
49 f libraries to provide a prediction of which trans -acting factors binding sites are disrupted/create
50  human immunodeficiency virus type 1 (HIV-1) trans- activation-responsive (TAR) RNA.
51 ffinity of r(K57D)K3 for the lysine analogue trans-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) wa
52 B-DNA complex formation was similar with (+)-trans- and (+)-cis-BPDE-adducted substrates, suggesting
53  study, we have measured the effects of all -trans- and 11- cis-retinals and -retinols on the opsin's
54 that RDH12 utilizes the unbound forms of all-trans- and 11-cis-retinoids.
55 mitoyl coenzyme A-dependent synthesis of all-trans- and 11-cis-retinyl esters.
56 ocols for the high-yielding synthesis of 2,3-trans- and 2,3-cis-6-methoxy-3-substituted morpholine-2-
57 sis and the stereoselective synthesis of 2,5-trans- and 2,6-trans-piperazines.
58                The vitamin A metabolites all-trans- and 9-cis-retinoic acid regulate gene expression
59  weak acid to give the 1,2-difurylethylenes, trans- and cis-1,2 di(2-(5-phenylfuryl))ethene (trans-1
60 uction" protocol was successfully applied to trans- and cis-2-methyl-N-(pyridin-2-yl)-6-undecylpiperi
61 573 K, and the relative epoxidation rates of trans- and cis-alkenes showed that calixarene ligands di
62 owever, we have successfully docked both the trans- and cis-amide isomers of the benzoquinone ansamyc
63 oxidoreductase 1 (NQO1) in the metabolism of trans- and cis-amide isomers of the benzoquinone ansamyc
64  results of these studies indicate that both trans- and cis-amide isomers of the hydroquinone ansamyc
65                                              trans- and cis-beta-Carotenes were analyzed by reversed-
66 arietal difference in carotenoids as well as trans- and cis-beta-carotenes were noted in both the raw
67 ports the analysis of total carotenoids, and trans- and cis-beta-carotenes, in different varieties of
68  product distributions from the reactions of trans- and cis-beta-methylstyrene reveal that the reacti
69 d for alpha, beta, and gamma isomers of HCH, trans- and cis-chlordane, oxychlordane, or SigmaCHB.
70 pounds determined in both air and water were trans- and cis-chlordanes (TC, CC), trans- and cis-nonac
71 obviating the usual requirement for both the trans- and cis-cinnamylsilanes.
72              The PL2 protease possessed both trans- and cis-cleavage activities, which were distingui
73 difference between the responses of Notch to trans- and cis-Delta: whereas the response to trans-Delt
74 romatography analysis, which can resolve the trans- and cis-diastereoisomers of alpha-(N(2)-deoxyguan
75                        The synthesis of both trans- and cis-diastereomers of pyrrolidinine-thioxotetr
76 emonstrated here would be useful to evaluate trans- and cis-elements that affect rate of the translat
77           The main phenolic acids in WF were trans- and cis-ferulic acids (257 and 165.57mg/100g dw,
78 type 1 (HIV-1) to CD4(+) T cells through the trans- and cis-infection pathways; however, little is kn
79 n elaborately designed process in which both trans- and cis-interactions are fine-tuned collectively
80 uces intercellular adhesion clusters through trans- and cis-intercadherin bonds, and the intracellula
81  a convenient reaction sequence for both the trans- and cis-isomers.
82  the aqueous ozonolysis reaction products as trans- and cis-lactols [4-(5-hydroxy-2,2-dimethyltetrahy
83 ter were trans- and cis-chlordanes (TC, CC), trans- and cis-nonachlors (TN, CN), heptachlor exo-epoxi
84                    Although the influence of trans- and cis-regulatory mutations is well known, the g
85      One key question concerns the extent of trans- and cis-regulatory variation in how co-expressed
86 RH transcription factors, but vary widely in trans- and cis-requirements for these inputs and their b
87 ulfide cross-links provide clear readouts on trans- and cis-SNARE arrangements during this fusion eve
88 m 3' splice site via exon definition in both trans- and cis-splicing systems.
89 ficant differences in total UCA content, and trans- and cis-UCA contents between the two samples.
90 s study, the amino acid, biogenic amine, and trans- and cis-urocanic acid (UCA) contents of fifteen c
91 nactivation of GRASP55-KR first affected the trans- and not the cis-Golgi.
92 ter of seven OR genes has been proposed as a trans- and pan-enhancer for OR gene expression.
93  barrier dysfunction that includes increased trans- and para-cellular leakage caused by impaired ente
94 in the transition structures determines high trans- and syn-diastereoselectivities for aldol reaction
95         The reaction is highly selective for trans- and trisubstituted alkenes and can be selective f
96 etone catalyst for asymmetric epoxidation of trans- and trisubstituted olefins was efficiently prepar
97 died catalysts, is an effective catalyst for trans- and trisubstituted olefins, and up to 97% ee has
98 nantioselectivity for hydroboration of cis-, trans-, and gem-disubstituted alkenes in excellent agree
99 eQTL) mapping by jointly utilizing cis-, cis-trans-, and trans-regulation.
100 in the highest quartile of trans-zeaxanthin, trans -anhydro-lutein, and trans-, cis-, and total beta-
101 [ a]pyrene-derived N (2)-dG adduct, 10 S(+)- trans- anti-[BP]- N (2)-dG ([BP]G*), reveal that an inco
102 he RPTPmu ectodomain that forms a homophilic trans (antiparallel) dimer with an extended and rigid ar
103 YP26A1, which catalyzes the oxidation of all-trans (at)-retinoic acid (RA), is induced moderately by
104 induced receptor dimerization and consequent trans- auto-phosphorylation are among the earliest event
105 ably efficient translesion bypass of the (+)-trans-[BP]-N(2)-dG adducts is observed in all sequences
106                       Thus the bypass of (+)-trans-[BP]-N(2)-dG adducts under conditions when [dNTP]
107  or even enhanced in the presence of the (+)-trans-[BP]-N(2)-dG adducts.
108 n cell signaling revealed that expression of trans- but not cis-null JAM-A mutants decreased Rap2 act
109 cular docking simulations indicated that the trans- but not the cis-amide isomers of the benzoquinone
110 ts the disassembly of SNARE complexes in the trans-, but not in the cis-, configuration.
111 hat consist of flavan-3-ol units such as 2,3-trans-(+)-catechin and 2,3-cis-(-)-epicatechin.
112  C. polonica revealed that the levels of 2,3-trans-(+)-catechin and PAs that are produced in the tree
113 orescence anisotropy analysis, for which the trans (cis) isomer in DOPC (DPPC) presents a fast decay
114 e variety of substituted styrenes, including trans-, cis-, and beta,beta-disubstituted styrenes, to y
115 ction was further studied by the reaction of trans-, cis-, and gem-ethylene-d2 upon activation of Cr(
116 trans-zeaxanthin, trans -anhydro-lutein, and trans-, cis-, and total beta-carotene had significant 43
117            They are Os(II)-dinitrogen (e.g., trans-, cis-, or fac-[Os(II)-N(2)]), Os(II)-nitrosyl [Os
118 nd Ac-NDP-gamma-MSH-NH(2) replaced by Pro or trans-/cis-4-guanidinyl-Pro derivatives were designed an
119 OH)](+)), and Os(IV)-methoxyhydrazido (e.g., trans-/cis-[Os(IV)-N(H)N(H)(OMe)](+), and trans-/cis-[Os
120 ., trans-/cis-[Os(IV)-N(H)N(H)(OMe)](+), and trans-/cis-[Os(IV)-N(H)N(Me)(OMe)](+)) adducts.
121 2))][PF(6)](2), 2[PF(6)](2), a derivative of trans-[Cl(dppe)(2)Ru(C triple bond C)(6)Ru(dppe)(2)Cl] f
122  MCl2; cagelike adducts of the in,in isomer, trans- Cl2(P((CH2)14)3 P) (M = 2/Pt, 3/Pd, 4/Ni), then f
123 ariants were identified that were encoded in trans (compound heterozygosity).
124 cts of both long-range intra-chromosomal and trans (cross-chromosomal) regulation, we observe modular
125 ost stable in vacuo, while the cis-trans-cis-trans (ctct) or trans-cis-trans-cis (tctc) amide conform
126 ts have been achieved using compounds with a trans-[CuX(4)Y(2)] coordination sphere, which seems to a
127 species could be attributed to both cis- and trans- DNA sequence changes during evolution, but it is
128 ngle configurational isomer, assigned to the trans (E) configuration.
129  rotary motors that harness photoinduced cis-trans (E-Z) isomerization are promising tools for the co
130 atory evolution in both cis (e.g., Creb) and trans (e.g., fork head) for nearly 2000 genes, many of w
131    As we expected, both significant cis- and trans- effects are responsible for the expression diverg
132  expression markers, by integrating cis- and trans- effects from many genomic loci, may overcome limi
133 one, two, or four cis (oleic or linoleic) or trans (elaidic or linoelaidic) double bonds.
134                                              trans-(-)-epsilon-Viniferin (viniferin), a natural produ
135                                  A series of trans-(FcC(2n))Ru(2)(Y-DMBA)(4)(C(2m)Fc) with n, m = 1 a
136 , CH2Cl2, reflux) give the cage-like trienes trans- Fe(CO)3(P((CH2)mCH horizontal lineCH(CH2)m)3 P) (
137 , 60-80 degrees C) yield the title compounds trans- Fe(CO)3(P((CH2)n)3 P) (4a-c,e, 74-86%; n = 2m + 2
138 )2)4) afford the metal hydride complexes mer,trans-[ Fe(CO)3(H)(P((CH2)n)3 P)](+)BArf(-) (6a-c,e(+)BA
139 n alcohol, new iron dicarbonyl complexes mer-trans-[Fe(Br)(CO)2(P-CH horizontal lineN-P')][BF4] (wher
140 atmosphere to produce the complexes cis- and trans-[Fe(Br)2(CO)(P-CH horizontal lineN-P')]; (2) the r
141 active system generated from the precatalyst trans-[Fe(CO)(Br)(Ph(2)PCH(2)CH horizontal lineN-((S,S)-
142 he mechanism of transfer hydrogenation using trans-[Fe(NCMe)CO(PPh(2)C(6)H(4)CH horizontal lineNCHR-)
143 s, leading to the formation of catechin [2,3-trans-(+)-flavan-3-ol] and epicatechin [2,3-cis-(-)-flav
144 e with their role in the biosynthesis of 2,3-trans-(+)-flavan-3-ols, transcript abundance of Norway s
145 t enzyme involved in the biosynthesis of 2,3-trans-(+)-flavan-3-ols, were identified and functionally
146 -handed all-cis (Form I) and left-handed all-trans (Form II), were determined in the crystalline stat
147          Baseline separation of the cis- and trans- forms of both hydroxyproline and fluoroproline wa
148   Importantly, expression of gB and gH/gL in trans (gB-expressing cells mixed with other gH/gL-expres
149  NMR dynamics studies show monomers with all trans (Gly-Pro-Hyp)(4) are less flexible than monomers c
150 ivity of aza-peptide epoxides is S,S > R,R > trans > cis.
151                         Azobenzene undergoes trans-->cis isomerization when irradiated with light tun
152 ups ortho to the azo group, exhibits minimal trans-->cis photoisomerization and extremely rapid cis--
153 structure of the retinal chromophore and all-trans --> 13-cis isomerization.
154 oreaction pathway that leads normally to all-trans --> 13-cis isomerization.
155 xhibit a high photochemical conversion rate (trans --> cis > 98%) and no measurable fatigue over a la
156                                      Pro-238 trans --> cis isomerization is not a simple on/off switc
157 contractions up to 13 A in the backbone upon trans --> cis photoisomerization.
158 and 19-20 kcal/mol for the cis --> trans and trans --> cis processes, respectively.
159 all isomeric states of an azobenzene moiety (trans --> cis-(M) --> cis-(P)) are passed step by step.
160 2 elimination the chlorostannylidene complex trans-[H(dmpe)2Mn horizontal lineSn(Cl)(C6H3-2,6-Mes2)]
161 tatively into the stannylidyne complex salts trans-[H(dmpe)2Mn identical withSn(C6H3-2,6-Mes2)]A [A =
162                                              trans-[(H(2)NCH(2)CH(2)C triple bond N)(dppe)(2)Ru(C tri
163 rmation of endo (4a) and exo (4b) isomers of trans-[HFe(PNHP)(dmpm)(CH(3)CN)](BPh(4))(2).
164                                  The complex trans-[HFe(PNP)(dmpm)(CH(3)CN)]BPh(4), 3, (where PNP is
165 eplication, some of which can be provided in trans (i.e., via expression from a separate RNA molecule
166 mechanistic study of the reaction of O2 with trans-(IMes) 2Pd(H)(OBz), 1 (IMes = 1,3-dimesitylimidazo
167 3-dimesitylimidazol-2-ylidene), which yields trans-(IMes) 2Pd(OOH)(OBz), 2.
168 plicable for large-scale mapping of cis- and trans- interaction networks of genomic elements and for
169                       To prove this concept, trans-/intramucosal and lymph-node delivery of PLGA-PEG
170 th both C-F and P-C bond activation to yield trans-[Ir(C6F5)(PEt3)2(PEt2F)], C2H4, and CH4.
171 onditions in CH3CN/TEOA, a common reactive C-trans-[Ir(tpy)(ppy)](0) species, irrespective of the sta
172                           Only one isomer, C-trans-[Ir(tpy)(ppy)H](+), reacts with CO2 to generate th
173                       Using a model species, trans-[IrMe(PH3)2(PH2Et)], a low-energy mechanism involv
174 d with the more electron-rich model reactant trans-[IrMe(PMe3)2(PMe2Et)] and the higher barriers foun
175 s were modeled using HCCR as weak acids, and trans-{kappaC,N-(3,4,5-(F)3-C6H2)CH2N horizontal lineCH(
176                 Asymmetric reductions in the trans [KCl] produced noticeable asymmetric shifts in the
177                                    As cis or trans [KCl] was reduced by 25%, 50%, or 75% relative to
178             To examine this question, cis or trans [KCl] was systematically lowered and the equilibri
179 ged from 0.61 at 25% cis [KCl] to 1.4 at 25% trans [KCl], with a Hill coefficient of 1.0.
180 2)(PhCN)(2)] afforded the Group 10 complexes trans-[MCl(2)(1)(2)] (3a-c, M = Ni, Pd, and Pt, respecti
181  crystal structures of a family of compounds trans-[MCl(2)(NC(5)H(4)X-3)(2)] (M = Pd(II), Pt(II); X =
182        DFT calculations on the model dimers {trans-[MCl(2)(NH(3))(NC(5)H(4)X-3)]}(2) show association
183 = N,N,N',N'-tetramethylethylenediamine) with trans-[MCl(2)(Pn-Bu(3))(2)] [M = Ni (trans-6a) and Pd (t
184  samples of the cyclic phosphazenes, cis- or trans-[Me(Ph)PN](3), yielded mixtures of the cis and tra
185 actors as mega transcription factor-bound in trans (MegaTrans) enhancers.
186  of its components, suggest that for G:C W:W Trans , Mg(2+) binding can fine tune the basepair geomet
187 lfide/peroxide bonds, relative to the end-on trans- micro -1,2 structure, which forms two bonds to th
188 -(-)-1a [cis-(-)-MR201], and trans-(+/-)-1a [trans-(+/-)-MR204], have been identified as new potent s
189 l effects on CHGA expression, and that a cis:trans (mRNA:miR) interaction regulates the association o
190 e activates the kinase domain of Stt7 on the trans (negative) side, leading to phosphorylation and re
191 ion of O2 into the palladium-hydride bond of trans-(NHC)2Pd(H)OAc (NHC = N-heterocyclic carbene).
192 n investigated for both mono- and bimetallic trans-(NHC)PtX2(amine) complexes.
193 omplexes featuring a single fluoride ligand (trans-[Ni(F)(2-C5NF4)(PR3)2], R = Et 1a, Cy 1b, trans-[P
194                             The synthesis of trans-[Ni(F){2-C5NF3(NH2)}(PEt3)2], which exhibits an ex
195 in a 1:1 ratio between cis (fluorescent) and trans (nonfluorescent) conformations.
196 ession in cis (in the sensory neurons) or in trans (on neighboring visceral mesoderm) transforms abdo
197 or interaction with both cis (same cell) and trans (opposite cell) ligands.
198 -bp oligonucleotides containing a single (+)-trans- or (+)-cis-BPDE adduct.
199 ls and cell membrane were incubated with all-trans- or 11-cis-retinol to study retinyl ester synthesi
200  dsDNA can serve as coenzymic DNA for PARP-1 trans- or auto-modification activity.
201 ng a saturated alpha-isoprene to unsaturated trans- or cis- alpha-isoprene units.
202      The stereoselective synthesis of either trans- or cis-3,5-disubstituted pyrazolidines is accompl
203 lyze the hydrolytic dehalogenation of either trans- or cis-3-haloacrylates to yield malonate semialde
204                          Treatment of either trans- or cis-4-N,N-dibenzylaminocyclohex-2-en-1-ol with
205                          Treatment of either trans- or cis-4-N-benzylaminocyclohex-2-en-1-ol with Cl3
206 (2)]), Os(II)-nitrosyl [Os(II)-NO](+) (e.g., trans- or cis-[Os(II)-NO](+)), Os(IV)-hydroxyhydrazido (
207                                              Trans- or cis-disubstituted alkenes can be used; alkyl-
208 the precursor alkene (i.e., monosubstituted, trans- or cis-disubstituted and cyclic alkenes).
209 orphyrin ligands or additives, giving either trans- or cis-dominant cyclopropanes.
210 c dihydroxylation is converted into either a trans- or cis-epoxide, and these are subsequently conver
211 onditions for maintenance of and invasion by trans- or cis-plus-trans-controlled hotspots are broader
212  Amino acid-dependent selectivity for either trans- or cis-substituted piperazinone products has been
213 at it represents an intermediate step in the trans- or dedifferentiation of neurons into astrocytes.
214 SR events occur between chromosome homologs (trans- or interallele CSR), suggesting that the homologo
215 chromosome kissing" between two DNA sites in trans (or in cis) is known to facilitate three-dimension
216 e)]PF(6) = [2]PF(6)), and phosphoraniminato (trans-[Os(IV)(Tp)(Cl)(2)(NP(H)(Et)(2))] = [3], Tp(-) = t
217 ydroquinone (H(2)Q) by the Os(IV) hydrazido (trans-[Os(IV)(tpy)(Cl)(2)(N(H)N(CH(2))(4)O)]-PF(6) = [1]
218  tpy = 2,2':6',2"-terpyridine), sulfilimido (trans-[Os(IV)-(tpy)(Cl)(2)(NS(H)-4-C(6)H(4)Me)]PF(6) = [
219 ions between the Os(VI)-nitrido salts (e.g., trans-[Os(VI)(tpy)(Cl)(2)(N)]PF(6) (tpy = 2,2':6',2"-ter
220 ization of the air-stable nickel(II) complex trans-(PCy(2)Ph)(2)Ni(o-tolyl)Cl is described in conjunc
221 ns-[Ni(F)(2-C5NF4)(PR3)2], R = Et 1a, Cy 1b, trans-[Pd(F)(4-C5NF4)(PCy3)2] 2, trans-[Pt(F){2-C5NF2H(C
222 on that kinetic factors inhibit formation of trans-[Pd(IMes)2(eta(1)-O2)2] at the low temperatures at
223 tion diagram is constructed for formation of trans-[Pd(IPr)2(eta(1)-O2)2] and leads to the conclusion
224 d(IPr)2(eta(2)-O2)] adds a second O2 to form trans-[Pd(IPr)2(eta(1)-O2)2].
225  with H2O in methanol/ether solution to form trans-[Pd(IPr)2(OH)(OOH)].
226                     The crystal structure of trans-[Pd(IPr)2(OOH)(OH)] is reported.
227 o detect the predicted T-shaped intermediate trans-[Pd(NHC)2(eta(1)-O2)] for either NHC = IMes or IPr
228 ic potential distributions for the compounds trans-[PdCl(2)(NC(5)H(4)X-3)(2)] (X = F, Cl, Br, I) demo
229 nsmetalation from 2 to [NiCl(2)(PPh(3))(2)], trans-[PdCl(2)(PhCN)(2)], or trans-[PtCl(2)(PhCN)(2)] af
230 cinchona alkaloid derivatives; surprisingly, trans-(Ph(3)P)(2)PdCl(2) was found to afford the most dr
231 3)Rh(F)] reacts with CF(3)SiMe(3) to produce trans-[(Ph(3)P)(2)Rh(CF(2))(F)] (1; X-ray), which is equ
232  conditions (3 h at 80 degrees C) to produce trans-[(Ph(3)P)(2)Rh(Ph(2)PF)(Cl)] (2) and ArPh as a res
233 degrees C), 1 decomposes to a 1:1 mixture of trans-[(Ph(3)P)(2)Rh(Ph(2)PF)(F)] (3) and the cyclometal
234 the thermodynamics of addition of methane to trans-(PH3)2IrX are generally strongly disfavored by inc
235 disfavors oxidative addition of N-H bonds to trans-(PH3)2IrX.
236 ons were performed on an extensive series of trans-(PH3)2IrXL complexes (L = NH3 and CO; X = various
237 form the palladium cyclopentylmethyl complex trans-[(phen)Pd[CH2CHCH2C(CO2Me)2CH2CHCH2SiEt3](NCAr)]+
238     Thus cis-(PMe(3))Cr(CO)(4)(H(2)) (3) and trans-(PMe(3))Cr(CO)(4)(H(2)) (4) were prepared and char
239 C(5)H(4)N)(2)-p-C(2)B(10)H(10) (1) and 1,12-(trans-(Pt(PEt(3))(2)I)CC)(2)-p-C(2)B(10)H(10) (2), are r
240 pped intermediates to the native molecule by trans-[Pt(en)(2)Cl(2)](2+) may be helpful in facilitatin
241  1a, Cy 1b, trans-[Pd(F)(4-C5NF4)(PCy3)2] 2, trans-[Pt(F){2-C5NF2H(CF3)}(PCy3)2] 3 and of group 4 dif
242    The octahedral Pt(IV) complex trans,trans,trans-[Pt(N(3))(2)(OH)(2)(py)(2)] (1) is potently cytoto
243  anticancer platinum(IV) complex trans,trans,trans-[Pt(N3 )2 (OH)2 (MA)(Py)] (MA=methylamine, Py=pyri
244 d, consequently, the cytotoxicity of cis,cis,trans-[Pt(NH3)2Cl2(O2CCH2CH2COOH)(OCONHR)], 4, where R i
245 ands (and carboxylate ligands in general) in trans-[Pt(OAc)(2)(L)(L')] results in significantly enhan
246                By use of XANES spectroscopy, trans-[Pt(OAc)2(ox)(en)] and trans-[PtCl2(OAc)2(en)] wer
247 )OH)(2)], trans-[PtCl(2)(s-PhobPBu)(2)], and trans-[PtCl(2)(a(7)-PhobPBu)(2)] are reported.
248 bPBu)(2)], (iii) (1)J(PtP) for the PEt(3) in trans-[PtCl(2)(PEt(3))(PhobPBu)].
249 2)(PPh(3))(2)], trans-[PdCl(2)(PhCN)(2)], or trans-[PtCl(2)(PhCN)(2)] afforded the Group 10 complexes
250 ]Cl(2), cis-[PtCl(2)(a(5)-PhobPCH(2)OH)(2)], trans-[PtCl(2)(s-PhobPBu)(2)], and trans-[PtCl(2)(a(7)-P
251 S spectroscopy, trans-[Pt(OAc)2(ox)(en)] and trans-[PtCl2(OAc)2(en)] were observed to be reduced at a
252 oduced instead, along with novel difluorides trans-[(Py)(2)Pd(F)(2)] (3) and trans-[(t-BuPy)(2)Pd(F)(
253                                    Complexes trans-[(Py)(2)Pd(Ph)(F)] (1; Py = pyridine) and trans-[(
254  Direct and selective mono-N-pyridylation of trans-(R,R)-cyclohexane-1,2-diamine is described here.
255        Our data support a mechanism in which trans- rather than cis-amide forms of benzoquinone ansam
256 -), cis-[Re(4)Os(2)Se(8)(CN)(6)](2-/3-), and trans-[Re(4)Os(2)Se(8)(CN)(6)](2-/3-) couples at E(1/2)
257   An S = 3/2, high-anisotropy building unit, trans-[ReCl(4)(CN)(2)](2-), representing the first param
258 urces of information, we identified putative trans- regulators for a variety of metabolic pathways.
259 ated carbon powder with one of the complexes trans-[ReO(2)(py-X)(4)](+) (py-X = 4-substituted pyridin
260 ) (1)J(PSe) for PhobP(Se)Bu; (ii) nu(CO) for trans-[RhCl(CO)(PhobPBu)(2)], (iii) (1)J(PtP) for the PE
261 mers (PAOs) with the general structure trans,trans-[(RO)3Ph-C[triple bond]C-Pt(PMe3)2-C[triple bond]C
262 u((R,R)-Me-DuPHOS)(2)(eta(2)-C(2)H(4))], and trans-[Ru((R,R)-Me-DuPHOS)(2)(C(6)F(5))(H)].
263 fac-[Ru(II)Cl(2)(DMSO)(3)(CTZ)] (1), cis,cis,trans-[Ru(II)Cl(2)(DMSO)(2)(CTZ)(2)] (2), Na[Ru(III)Cl(4
264 I analogs of a general structure [4-R-pyH](+)trans-[Ru(III)Cl4(DMSO)(4-R-py)](-), where 4-R-py stands
265 odefluorination (HDF) of fluoroarenes by the trans-[Ru(IMe4 )4 H2 ] catalyst, 3, is reported.
266 ammatory activity of ruthenium(II) complexes trans-[Ru(NO(+))(NH3)4(L)](BF4)3 and [Ru(NH3)5(L)](BF4)3
267 ld (Phi(S)(-->)(O) = 0.25), isomerization of trans-[Ru(tpy)(pic)(dmso)](+) occurs with a time constan
268                                          For trans-[Ru(tpy)(pic)(dmso)](+), global analysis of the tr
269 xes [Ru(tpy)(bpy)(dmso)](OSO(2)CF(3))(2) and trans-[Ru(tpy)(pic)(dmso)](PF(6)) (tpy is 2,2':6',2' '-t
270 nation of acetophenone by the chiral complex trans-[RuCl2{(S)-binap}{(S,S)-dpen}] and KO-t-C4H9 in pr
271 CHPh)2NH2}] and the 18e(-) Ru alkoxo complex trans-[RuH{OCH(CH3)(R)}{(S)-binap}{(S,S)-dpen}] (R = CH3
272  of the Noyori ketone hydrogenation catalyst trans-[RuH2((R)-BINAP)((R,R)-dpen)] (1a) yields trans-M[
273 -[RuH2{(S)-binap}{(S,S)-N(K)H(CHPh)2NH2}] or trans-[RuH2{(S)-binap}{(S,S)-N(K)H(CHPh)2NH(K)}].
274 formation of the potassium amidato complexes trans-[RuH2{(S)-binap}{(S,S)-N(K)H(CHPh)2NH2}] or trans-
275               Resveratrol (3,5,4'-trihydroxy-trans -stilbene) is a well-known polyphenolic compound o
276 e example is the 1:1 charge-transfer complex trans--stilbene-2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoqu
277 on reaction and the ratio of trans,cis/trans,trans (t,c/t,t)-conjugated diene oxidation products form
278  difluorides trans-[(Py)(2)Pd(F)(2)] (3) and trans-[(t-BuPy)(2)Pd(F)(2)] (4).
279 ns-[(Py)(2)Pd(Ph)(F)] (1; Py = pyridine) and trans-[(t-BuPy)(2)Pd(Ph)(F)] (2; t-BuPy = 4-tert-butylpy
280 ticancer agents, especially NKP-1339 (sodium trans-[tetrachloridobis(1H-indazole)ruthenate(III)]), wh
281                                   Indazolium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (1, KP
282 te(III)] (1, KP1019) and its analogue sodium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (2, KP
283 especially the clinically studied indazolium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (KP101
284 enate(III)] (KP1019) and its analogue sodium trans-[tetrachlorobis(1H-indazole)ruthenate(III)] (NKP-1
285             The anticancer ruthenium complex trans-[tetrachlorobis(1H-indazole)ruthenate(III)], other
286                  The organometallic compound trans-(tetrafluoropyrid-2-yl)bis(triethylphosphine)-fluo
287               Our results show that both the trans- TF features and the cis- motif features are predi
288 ch indicates that mitofusin complexes act in trans (that is, between adjacent mitochondria).
289 cis (the GlnRS N-terminal Yqey domain) or in trans (the Arc1p protein associating with GluRS).
290 mains of both the cis (GS(m)-bound ring) and trans (the opposite substrate-free ring) show counterclo
291 ly transformed to the corresponding cis- and trans- title compounds, respectively.
292 th the low thermal activation barrier of the trans- to cis-isomerization typical for imine derivative
293 -12)) and one variant regulating 53 genes in trans (top trans interaction: ZNF423, rs3851570, p = 8.2
294 s (28), one singly trans (29), one quintuply trans (trannulene-type, 33), and one all-cis (31).
295 s and presents IL-15 to neighboring cells in trans (trans-presentation of IL-15) through cell-cell co
296     This study revealed the preferential all-trans (TTT) conformation of the three ethylenedioxy link
297 ry that two aspects of lectin functionality (trans- versus cis-activity) respond non-uniformly to a s
298                         Here, we examine how trans- versus cis-silenced genes in a somatic cell type
299 s N1 cyclization) and the stereoselectivity (trans- vs cis-fused ring system) of the cyclization proc
300 he form H(2)[pz(A(4-n);C(n))], n = 1, and 2 (trans-), where "A" represents peripheral heteroatom (S-

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