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1 complete chemoselectivity (exclusive [2 + 2] photoproduct).
2 rent species (reactants and initially formed photoproducts).
3 usion of the metastable leuco-methylene blue photoproduct.
4  discovery of 2,8-dichlorodibenzodioxin as a photoproduct.
5 g the UV-induced pyrimidine-pyrimidone (6-4) photoproduct.
6 observed to contain detectable levels of any photoproduct.
7  token ligand to two spin states of the same photoproduct.
8 e dimers (CPDs), the primary ultraviolet DNA photoproduct.
9                The other state is an ICT-EPT photoproduct.
10 abatic relaxation to the ground state of the photoproduct.
11 crystallography to further characterize this photoproduct.
12  constitute the most frequent UV-induced DNA photoproduct.
13 taining the phenolate group becomes the sole photoproduct.
14 onds 5' and 5 phosphodiester bonds 3' to the photoproduct.
15 5'-N, 3'-S conformer gives rise to the (6-4) photoproduct.
16 t in the electronically excited state of the photoproduct.
17 ng to [Cl2Sb(IV)Pt(I)Cl(o-dppp)2] (1) as the photoproduct.
18 ood pathways that can culminate in mutagenic photoproducts.
19 ference for an adenosine downstream from 6-4 photoproducts.
20 o a lesser extent, affects the repair of 6-4 photoproducts.
21  for the dioxin, biphenyl, and phenoxyphenol photoproducts.
22 ost-photochemical transformations of primary photoproducts.
23 assess the fate of TBA metabolites and their photoproducts.
24 ssipating excess photoenergy and deleterious photoproducts.
25 ormation of emissive spectrally blue-shifted photoproducts.
26 leavage and the formation of highly oxidized photoproducts.
27 ly formed via subsequent reaction of primary photoproducts.
28 pplied radioactivity) and smaller amounts of photoproducts.
29 c acid, increasing the diversity of observed photoproducts.
30 emphasis was placed on identification of the photoproducts.
31 volunteers in vivo, whereas UVB induced both photoproducts.
32 ttack on cancer cells by radicals and Pt(II) photoproducts.
33 r PARP activity in the repair of UVR-induced photoproducts.
34  energy and prevent the formation of harmful photoproducts.
35 hen DNA is replicated before repair of these photoproducts.
36 sylase that can initiate BER of dipyrimidine photoproducts.
37 ty in MC and XP cells for ODD and UV-induced photoproducts.
38 rm the respective carbodiimides 5a,b as sole photoproducts.
39 n repair of replication forks stalled at DNA photoproducts.
40 h no effect was observed for repair of (6-4) photoproducts.
41 se might be responsible for the diversity of photoproducts.
42  -distorting DNA lesions, such as UV-induced photoproducts.
43 ion of oxidative modifications in bacitracin photoproducts.
44 imers (CPDs) and pyrimidine-pyrimidone (6-4) photoproducts.
45 induced DNA lesions, namely, thymidine (6-4) photoproducts.
46 arlier results reporting ketones as the main photoproducts.
47 excited states in DNA that lead to mutagenic photoproducts.
48 ed manually generating a suspect list of 108 photoproducts.
49 s C in aqueous NaOH forms three substitution photoproducts: 2-methoxy-5-nitrophenol (2), 2-chloro-4-n
50 n authentic samples of two of the identified photoproducts, 5-chloro-methylaminobenzophenone and 2-am
51                               The tryptophan photoproduct 6-formylindolo[3,2-b]carbazole (FICZ), an a
52 CPD), but not of pyrimidine (6, 4)pyrimidone photoproducts (6-4PP) following UV irradiation of mammal
53 imers (TTs), and pyrimidine (6-4) pyrimidone photoproducts (6-4PPs) in DNA.
54 wo containing pyrimidine (6-4')-pyrimidinone photoproducts ([6-4]s).
55 let (UV)-induced (6-4) pyrimidine-pyrimidone photoproduct [(6-4) PP] confers a large structural disto
56 24, and 48 h) and (6-4)pyrimidine-pyrimidone photoproducts [(6-4)PPs] (at 5 and 20 min and 1, 2, and
57 imers (CPDs) and pyrimidine-pyrimidone (6-4) photoproducts [(6-4)PPs] from UV-irradiated cellular and
58 imers (CPDs) and pyrimidine (6-4) pyrimidone photoproducts [(6-4)PPs] that must be repaired for the s
59 clobutane pyrimidine dimers (CPDs) and (6-4) photoproducts [(6-4)PPs], based on direct UV absorption
60 imers (CPDs) and (6-4) pyrimidine-pyrimidone photoproducts [(6-4)PPs].
61 diation on DNA is the formation of the (6-4) photoproduct, 6-4PP, between two adjacent pyrimidine rin
62 rimidine dimers, pyrimidine (6-4) pyrimidone photoproducts (64PPs) and their related Dewar valence is
63 ormed, which cyclizes to stable naphthofuran photoproducts 9-12.
64                                          Two photoproducts accounted for 15-30% of radioactivity in t
65 o metarhodopsin-II-like species and aberrant photoproduct accumulation with prolonged illumination.
66  these unique nonadjacent anti thymine dimer photoproducts also form in vivo, they would constitute a
67 an alter ovarian follicular development, and photoproducts alter whole-body 17beta-estradiol levels.
68 stem cells (CD34LC) were treated with the UV photoproduct and AhR ligand 6-formylindolo[3,2-b]carbazo
69 lindolo[3,2-b]carbazole (FICZ), a tryptophan photoproduct and endogenous high-affinity aryl hydrocarb
70  <or=1 nm, limits aggregation of the primary photoproduct and favors smaller particles.
71  ps to 1 ns within the spectral range of the photoproduct and is attributed to an equilibration betwe
72 etical study of the reaction between the NH2 photoproduct and O2 in the presence of H2O supports the
73 on adds to MV(2+) to form a covalently bound photoproduct and, subsequently, evolves toward a conical
74 ing 2H-azirine 3 and ketenimine 6 as primary photoproducts and also to nitrile ylide 4 and 2,5-dimeth
75 reactive oxygen species (ROS) as well as 6-4-photoproducts and cyclobutane pyrimidine dimers (CPD) in
76 mage sites; and (iv) increased repair of 6-4 photoproducts and cyclobutane pyrimidine dimers.
77 olesions such as (6-4) pyrimidine-pyrimidone photoproducts and cyclobutane pyrimidine dimers.
78 degradation and the bioactivity of resulting photoproducts and metabolites, pesticide photochemistry
79                          Accumulation of the photoproducts and sulfamethazine in sediment may have im
80  (320-400 nm) irradiation-induced ODD and UV photoproducts and the repair capacity in MC and XP cells
81 s the sole pathway in humans for removing UV photoproducts, and DNA replication are regulated by the
82 is of the QD-molecule systems shows that the photoproduct aniline, left unprotonated, serves as a poi
83 bovine serum albumin (BSA), and intermediate photoproducts are allowed to decay, mouse rods are stabl
84                                        These photoproducts are important oxidants and reactants in su
85 UVA/6-TG, indicating that potentially lethal photoproducts are not selectively excised from transcrib
86                             UV light-induced photoproducts are recognized and removed by the nucleoti
87 ma, suggesting that sunlight-induced "bulky" photoproducts are responsible for melanomagenesis.
88          The resultant photostable secondary photoproducts are subject to thermal dehydration in dark
89                      This indicates that DNA photoproducts are the most important premutagenic lesion
90 cological implications by characterizing the photoproducts arising from the direct photolysis of 17be
91 t previously been characterized nor have any photoproducts arising from this transition been identifi
92        This analogue gives rise to the (6-4) photoproduct as efficiently as the dithymine dinucleotid
93                            The biogenesis of photoproduct-associated siRNAs involves the noncanonical
94 FS, and XANES results give no indication the photoproducts bind to either silica matrix, and consolid
95 mation of two distinct solvated monocarbonyl photoproducts, both of which arise from the same triplet
96               In both mechanisms, the direct photoproduct Br(*) subsequently reacts with Br(-) to yie
97 ase excision repair of pyrimidine-pyrimidine photoproducts but produce all the other proteins require
98 cleotide excision repair (NER) removes these photoproducts, but whether NER functions at telomeres is
99 etylated and this enhances the repair of DNA photoproducts by the nucleotide excision repair (NER) pa
100 amage, cyclobutane pyrimidine dimers and 6,4-photoproducts, by facilitating DNA repair.
101 ion can greatly exceed the rate at which the photoproduct can be recycled back to the chromophore by
102                                              Photoproducts can also react to produce structural analo
103                         The formation of the photoproducts can be attributed to photoinduced oxidatio
104  that the formation of blue-shifted emissive photoproducts can have implications for analyzing single
105  in promoting replication through a (6-4) TT photoproduct carried on a duplex plasmid where bidirecti
106 Stat3 influenced the survival of ultraviolet-photoproduct cells, including those located in the hair
107  ranging from 310 to 500 nm reveal two major photoproduct channels corresponding to homolysis of aryl
108 o effect on the identity of the two dominant photoproduct channels.
109 elomeres exhibit approximately twofold fewer photoproducts compared with the bulk genome in cells, an
110 3 ps, whereas the rest goes on to the Lumi-R photoproduct consistent with the 15% photochemical quant
111 hat were no longer photoactive, with primary photoproducts consisting of monohydroxy species and pres
112 chemiluminescent detection of the excised UV photoproduct-containing oligonucleotides that are releas
113 nt spin state equilibrium in the 16-electron photoproduct CpCo(CO).
114 ron and proton transfer steps, the resulting photoproduct decays via concerted PCET (tau = 4.7 mus) w
115 an spectroscopy of the corresponding trapped photoproduct demonstrates that this rapidly formed P1 in
116                            Occurrence of new photoproducts derived from desulfonation and/or denitrif
117 lysis of these materials yields a mixture of photoproducts deriving from the presence of both carbene
118 delayed appearance after that of the primary photoproduct, diiodide radical I2(*)(-), indicates that
119 y translocated to sites of UVR-induced (6-4) photoproduct DNA damage in the nucleus.
120 ry complex, and time-resolved probing of the photoproduct dynamics by using ultraviolet-visible absor
121  cob(II)alamin-5'-deoxyadenosyl radical pair photoproduct, either through an increased barrier to rec
122 dent manner, showing that the presence of UV photoproducts enhances spontaneous unwrapping of DNA fro
123 aging agents such as UV light (generating UV photoproducts), ethyl methanesulfonate (generating alkyl
124 at UV-stalled replication forks, it promotes photoproduct excision, suppression of translesion synthe
125  CBCRs; some examples were stable as the 15E photoproduct for days, while others reverted to the 15Z
126 d axis of a nucleosome and find that whereas photoproduct formation and deamination is greatly inhibi
127                   We have now determined the photoproduct formation and deamination rates for 10 cons
128 nospot blotting to examine the efficiency of photoproduct formation and removal at telomeres purified
129 e-binding protein TRF1 significantly reduces photoproduct formation in telomeric fragments in vitro.
130                                              Photoproduct formation was also highly suppressed at one
131 ctural reorganization of Cph1 during primary photoproduct formation.
132 oth the quantum yield and the selectivity of photoproduct formation.
133 inguish between sites of cyclobutane and 6-4 photoproduct formation.
134 site cyclobutane pyrimidine dimers and (6-4) photoproducts formed at the TT, TC, and CC dipyrimidine
135 2)) during all the experiments, and the main photoproducts formed were characterized through accurate
136          The spectral properties of emissive photoproducts, formed upon 633 nm irradiation of a terry
137 the sole mechanism for removing the major UV photoproducts from genomic DNA in human cells.
138 or some Delta-S,S-Ru2H(2)/Lambda-R,R-Ru2H(2) photoproducts from Lambda to Delta (or vice versa) while
139 sion repair pathway removes ultraviolet (UV) photoproducts from the human genome in the form of short
140 ally excited molecules instead form a stable photoproduct G*C* that has undergone double hydrogen-ato
141                     Acidic hydrolysis of the photoproduct gave a product with the same retention time
142 s have a reduced repair capacity for ODD and photoproducts; H(2)O(2) modified- and UVC-irradiated DNA
143 ionalities, and interestingly, the resulting photoproducts had spectral characteristics similar to th
144 rine bacteria, and unlike the latter, the VF photoproduct has no measurable affinity for iron.
145 ional characterization of both reactants and photoproducts has been undertaken.
146                         These green emissive photoproducts have spectral properties that resemble tho
147 oncentrations of the still-bioactive primary photoproduct hydroxylated 17alpha-TBOH, produced via pho
148 UVA in the induction of ODD but not bulky UV photoproducts; (ii) the high susceptibility to UVA-induc
149 (GTATCATGAGGTGC) gave rise to an unknown DNA photoproduct in approximately 40% yield at acidic pH of
150 ies determine the spin state of the CpCo(CO) photoproduct in solution on the picosecond time scale.
151 n the ratio between the different classes of photoproducts in basal and induced DNA damage suggests t
152 wavelengths of light induce the formation of photoproducts in DNA that are potentially mutagenic if n
153 s use blue light to reverse UV-induced (6-4) photoproducts in DNA.
154 tastatic melanoma cells to repair UV-induced photoproducts in DNA.
155 ate TLS across cyclobutane pyrimidine dimers photoproducts in living cells, presenting a novel role o
156     To better define the nature of these DNA photoproducts in marine bacterioplankton and eukaryotes,
157            Sunlight UV exposure produces DNA photoproducts in skin that are repaired solely by nucleo
158 uch as cyclobutane pyrimidine dimers and 6-4 photoproducts in skin.
159  ring closure leading to bicyclo-beta-lactam photoproducts in solution.
160 epair of carcinogenic UV irradiation-induced photoproducts in the DNA, such as cyclobutane pyrimidine
161  presence and cycling of altrenogest and its photoproducts in the environment.
162 tifacts due to rotation of rhodopsin and its photoproducts in the membrane, probe light in the time-r
163 oate series; (2) their transformation to the photoproducts in the pentaenoate and then mycolactone se
164  via (1) structure determination of the four photoproducts in the tetraenoate series; (2) their trans
165                     As a result, the primary photoproducts in the xerogel do not achieve sufficient s
166 s for the first time the production of these photoproducts in UV irradiated mushrooms.
167 derlines the pivotal role of UVA-induced DNA photoproducts in UVA mutagenesis and carcinogenesis.
168 ions and nucleotide excision repair of (6-4) photoproducts in vitro.
169 mage, including cyclobutane dimers and (6-4) photoproducts, in the etiology of melanoma.
170 et reactivity for 16-electron organometallic photoproducts, in which triplets were not believed to in
171 sis of triclosan resulted in several primary photoproducts including the following: 2,8-dichlorodiben
172                          A total of fourteen photoproducts, including benzophenones, acridinones and
173                               In vitro, 6-TG photoproducts, including the previously characterized gu
174                              Analysis of the photoproducts indicated the deoxygenation occurred by at
175 he (6-4) pyrimidine:pyrimidone [(6-4) Py:Py] photoproducts induced by UVB/C radiation.
176 diation with 254 nm light indicates that the photoproduct is a cyclobutane thymine dimer.
177 sorbing like that of phytochrome but the 15E photoproduct is instead green-absorbing.
178  at 500 +/- 10 nm, an electron-transfer (ET) photoproduct is observed to form with a time constant of
179  containing a cis-syn TT dimer or a (6-4) TT photoproduct is severely inhibited in human cells and th
180                          In the case of this photoproduct, it appears that spin crossover does not pr
181 Cyclobutane pyrimidine dimers (CPDs) are DNA photoproducts linked to skin cancer, whose mutagenicity
182                                  The charged photoproducts locally perturb electroneutrality due to d
183                     Formation of the primary photoproduct Lumi-R is not affected by changes in solven
184  excited-state population, while the initial photoproduct Lumi-R was depleted by only 11%.
185                                        Spore photoproduct lyase (SPL) repairs 5-thyminyl-5,6-dihydrot
186                                        Spore photoproduct lyase (SPL) repairs a covalent UV-induced t
187 SAM (S-adenosylmethionine) enzyme, the spore photoproduct lyase (SPL), at the bacterial early germina
188  and repaired by a radical SAM enzyme, spore photoproduct lyase (SPL), at the early germination phase
189 ir of accumulated damage by the enzyme spore photoproduct lyase (SPL).
190 derivatives, most of the aldehyde and ketone photoproduct mass spectra observed from the aqueous phas
191              Furthermore, these unusual anti photoproducts may be used to establish the presence of G
192 nts of the azido probes even in the inactive photoproduct Meta I, well before the active receptor sta
193 oplasmic surface to form the active receptor photoproduct Meta II.
194  motif and the possibility that this type of photoproduct might also form in other folded structures,
195 cate that low concentrations of 17alpha-TBOH photoproduct mixtures can alter ovarian follicular devel
196 ed that transcription-coupled repair of both photoproducts occurs exclusively on the template strand.
197              Furthermore, the solvated Re(I) photoproduct of CO release (2) is also luminescent, a fe
198 , indicating that I(2)(-*) was not a primary photoproduct of excited state electron transfer.
199 3,4-dihydroxybenzoic acid (3,4-DHB), and the photoproduct of FePB (FePB(nu)) also mediate iron delive
200 ein YclQ, are unable to use either PB or the photoproduct of FePB (FePB(nu)) for iron delivery and gr
201 s identified as a significant and stable UVA photoproduct of free 6-TG, its 2'-deoxyribonucleoside, a
202 Here we show that the 221 cm(-1) mode of the photoproduct of iNOS(P420) does not exhibit any H(2)O-D(
203                              As a likely UVB photoproduct of intracellular tryptophan, FICZ represent
204    Although thymidine is the predominant UVA photoproduct of S(4)TdR in dilute solution, more complex
205 rmylindolo[3,2-b] carbazole (FICZ), is a UVB photoproduct of tryptophan and a powerful UVA chromophor
206 mistry and photosynthetic dynamics--in which photoproducts of chemical and biochemical reactions can
207           As a proof-of-concept, fluorescent photoproducts of the hydroxyindoles, 5-hydroxytryptamine
208                    Isolation and analysis of photoproducts of these diazochlorins formed within n-but
209 se phase HPLC compared to known dipyrimidine photoproducts of this sequence.
210 ng to reversion to the primary cycloaddition photoproduct on a time scale of hours to days, with the
211 yminyl-5,6-dihydrothymine (also called spore photoproduct or SP) is the exclusive DNA photodamage pro
212 yl-5,6-dihydrothymine (commonly called spore photoproduct or SP) is the exclusive DNA photodamage pro
213 minyl)-5,6-dihydrothymine, also called spore photoproduct or SP, is commonly found in the genomic DNA
214 re easily contaminated by contributions from photoproducts or higher excitons.
215  abasic site, a cis-syn TT dimer, a (6-4) TT photoproduct, or a G-AAF adduct--we show that Rad5 is ne
216 tion of 5-thyminyl-5,6-dihydrothymine (spore photoproduct, or SP), coupled with the efficient repair
217                   The observation of heme-CO photoproduct oscillations is unusual because most other
218 rent wavepacket motion in the bathorhodopsin photoproduct over the full vibrational manifold.
219 r periphery of the particle, and the primary photoproduct oxidizes, forming only Fe(2)O(3).
220                            The corresponding photoproducts PhBNN and PhBCO have triplet electronic gr
221                The sole isolated interlocked photoproduct (Phi = 0.06) is a [2]rotaxane, with the dim
222 taining cyclobutane pyrimidine dimers or 6-4 photoproducts photolesions.
223                             All porphyrinoid photoproducts possess intense absorption bands throughou
224 er of forms of damage in DNA, of which (6-4) photoproducts present the most formidable challenge to D
225 ring RNAs (siRNAs) in the recognition of DNA photoproducts, prevalently in intergenic regions.
226        In this study, the ergosterol-derived photoproducts previtamin D(2), lumisterol(2) and tachyst
227               The stereogenic methine on the photoproduct, rac-2-(p-hydroxyphenyl)propanoic acid (rac
228 he protein binding site therefore suppresses photoproduct radical pair formation.
229 samples of large amounts of DEWs, a class of photoproducts rarely considered outside photochemical st
230 ir proteins survey the genome for UV-induced photoproducts remains a poorly understood aspect of the
231 ound that although p53 status contributed to photoproduct removal efficiency, its role did not seem t
232 that the Ino80-C contributes to efficient UV photoproduct removal in a region of high nucleosome occu
233 protein indicates the mechanism of telomeric photoproduct removal is NER.
234  similarly increased XPC mRNA expression and photoproduct removal with less toxicity than with the am
235 ess to diverse core scaffolds in the primary photoproducts, rendering the approach compatible with th
236 ently available methods for investigating UV photoproduct repair in vivo, we developed a convenient n
237 ithout diminishing cellular UV resistance or photoproduct repair in vivo.
238 t in 11 of 12 melanoma cell lines tested, UV photoproduct repair occurred as efficiently as in primar
239 ymes responsible for NER, did not accelerate photoproduct repair.
240 xidized 6-TG and a previously identified UVA photoproduct--replaces 6-TG, suggesting that G(SO3) is a
241 e generation or enhancement of repair of DNA photoproducts, respectively.
242 play a crucial role for obtaining long-lived photoproducts resulting from multiphoton, multielectron
243 r, it is often thought that any diversity of photoproducts results from different conical intersectio
244 one receptor screening revealed that certain photoproducts retain significant androgenic activity, wh
245 fter visible irradiation, SFM imaging of the photoproducts revealed both the structural implications
246 e 1.55 A resolution crystal structure of the photoproduct reveals retention of the O-binding mode for
247 deoxyuridine and pyrimidine (6-4) pyrimidone photoproduct, reveals that neither reaction is reversibl
248 n was used to quantify the appearance of two photoproducts [Ru(bpz(-))(bpz)(deeb)](+) and I(2)(-*).
249 ch that neither the carbonyl complex nor its photoproduct(s) exits the polymer at any time.
250           Loss of either the nitrosyl or its photoproduct(s) from these materials in biological media
251 y) in the reactant to point chirality in the photoproduct(s).
252                                  The primary photoproducts-secondary or tertiary anilines which are n
253 nes, suggesting that the fate and effects of photoproducts should also be incorporated into future ri
254                     Interestingly, these two photoproducts showed relatively higher persistence than
255 hermore, spectral analysis of the melanopsin photoproduct shows the formation of a protonated metarho
256 s a covalent UV-induced thymine dimer, spore photoproduct (SP), in germinating endospores and is resp
257  thymine dimer that is also called the spore photoproduct (SP), in germinating endospores.
258 othymine, which is commonly called the spore photoproduct (SP), the Cadet laboratory found an incompl
259 thyminyl-5,6-dihydrothymine, i.e., the spore photoproduct (SP).
260 othymine, commonly referred to as the "spore photoproduct" (SP), and 5,6-dihydro-2'-deoxyuridine (dHd
261             Facile hydrolysis of the primary photoproducts, spiro-oxazolidines and thiazolidines, und
262 otolysis in CooA, which revealed very strong photoproduct state coherent oscillations.
263                                        Three photoproduct states are populated following a saturating
264      Our results will allow disentangling of photoproduct states in flavoproteins in often-encountere
265                                        Three photoproduct states, P(f), P(s), and P(c), are identifie
266 ral similarity to parent steroids, and these photoproducts still retain enough biological activity to
267                               The long-lived photoproduct stores energy in the form of a radical pair
268 efficient formation of this interstrand-type photoproduct suggests the existence of a new type of fol
269         The X-ray structure of silyl hydride photoproducts suggests a residual H(1)...Si(1) interacti
270 oheptane thioketones by (1)O2 can yield more photoproducts than exclusively ketones and sulfines.
271 wledge, the first observation of a transient photoproduct that exhibits an equilibrium between two st
272 roposed where an iodine atom was the primary photoproduct that subsequently reacted with iodide, I(*)
273 sulting in chemically reduced and persistent photoproducts that are likely to exhibit transport and t
274 ndiscriminate, leading to a large mixture of photoproducts that are observed using high-resolution el
275 om cyclobutane pyrimidine dimers (CPDs), DNA photoproducts that are typically created picoseconds aft
276 of the tolerance of the UV light-induced 6-4 photoproduct, the tobacco smoke-induced benzo[a]pyrene-g
277                         This approach allows photoproducts to be detected free from interferences fro
278 lations, allow us to assign the two solvated photoproducts to singlet and triplet CpCo(CO)(solvent) c
279                                   Mapping of photoproducts to the hormone-binding domains of the insu
280 by a quantum chain process where the excited photoproducts transfer energy to neighboring molecules o
281 n determined that this primary cycloaddition photoproduct undergoes photohydration.
282                  The high selectivity in the photoproduct upon reaction from the triplet excited stat
283                The enantioselectivity in the photoproducts varied from 22 to 95% depending on the rea
284 hemical capstone modification of the primary photoproducts via Suzuki coupling provides rapid access
285                                  The primary photoproduct was identified as an isomer formed via an i
286 verse photoconversion of the green-absorbing photoproduct was not significant in restoring the dark s
287   The percent conversion to dioxin and other photoproducts was determined and the natural product, 6-
288 f PUV irradiation and the formation of major photoproducts was observed to increase as a function of
289                The repair of UV-induced (6-4)photoproducts was severely impaired in these cells, and
290                                          The photoproducts were identified (i) by comparison with inf
291               Between two and nine confirmed photoproducts were identified for SMX-metabolites throug
292                  Over 80 aldehyde and ketone photoproducts were observed from scan range 200-1000 ato
293                          Aldehyde and ketone photoproducts were observed in the aqueous phase under o
294 r column at the end of the 63-day study; the photoproducts were the major degradates in the aqueous a
295 e dimers (CPD) and pyrimidine(6-4)pyrimidone photoproducts, which interfere with DNA replication and
296 ion, leading to two regioisomeric (exo/endo) photoproducts with complete chemoselectivity (exclusive
297          Therefore, direct photolysis yields photoproducts with strong structural similarity to paren
298  retinal binding pocket, converting into the photoproduct within about 100 ps, whereas the blue form
299                                          The photoproducts within these porous silica matrices reflec
300 r structural features of aldehyde and ketone photoproducts without interference from the many tens of

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