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1 his paper, we report the formation of highly electrophilic 1,1-deactivated olefins, their use as nove
2 nes with triflic anhydride (Tf(2)O) forms an electrophilic 1-trifloyl-aziridin-2-yl triflate species
3 oup, oxidation of an alpha-boryl radical, or electrophilic activation of an alkenyl boronate complex.
4 the concept of boronic acid catalysis (BAC), electrophilic activation of carboxylic acids leads to th
5                                          The electrophilic activation of double bonds in the bicyclic
6                               The C-terminal electrophilic activation of peptides by alpha-thioesteri
7   The opening of epoxides typically requires electrophilic activation, and subsequent nucleophilic (S
8  Together, these observations show that more electrophilic active-oxygen species (i.e., lower-energy
9 roperoxy derivative 7'' that evolved into an electrophilic acyl azolium, opening to the aldehyde-to-e
10  a vinyl cation from arylglyoxal and alkyne, electrophilic addition of the vinyl cation to the ipso c
11 as synthesized using a straightforward click/electrophilic addition or click/oxidative coupling tande
12 b (m/z 295 and m/z 323, respectively) via an electrophilic addition pathway.
13 tu under catalytic hydrogenation conditions, electrophilic addition to the keteniminate was achieved
14  describe a panel of novel C3-symmetric tris-electrophilic agents and their use for the cyclization o
15 A showed increased tolerance to oxidants and electrophilic agents.
16 al Cu(II)-bisoxazoline catalysts initiate an electrophilic alkene arylation, triggering a 1,2-alkyl m
17  acid from the 4-position to afford a highly electrophilic alkenediazonium ion.
18   A novel reaction of tetranitromethane with electrophilic alkenes in the presence of triethylamine a
19 s, with alpha,beta-unsaturated aldehydes and electrophilic alkenes proceed with total periselectivity
20 polar cycloaddition between imino esters and electrophilic alkenes, employing chiral metal complexes
21 is process provides the heterocyclization of electrophilic alkenes.
22 , this ligand-free CrCl(2) enables efficient electrophilic alkenylations of primary, secondary, and t
23  nucleophilic attack at the less substituted electrophilic alpha'-carbon.
24 based key intermediates including a 1,4-(bis)electrophilic alpha,beta-unsaturated ketenyl phosphonium
25 egrees C generated in situ the corresponding electrophilic alpha-trifluoromethyl N-acyliminium ions t
26                               In the case of electrophilic amidyl radicals, cascade processes involvi
27 d is dependent on the generation of a potent electrophilic aminating agent released by in situ deprot
28                This copper can react with an electrophilic aminating reagent, 1,2-benzisoxazole, to p
29                                    Attempted electrophilic amination of aromatics such as benzene and
30  describe a chiral phosphoric acid catalyzed electrophilic amination of enecarbamates with dibenzyl a
31  the enantioselective tandem three-component electrophilic amination of enecarbamates.
32                                              Electrophilic amination often requires a disparate toolk
33 ly formation of the heterotricyclic core, an electrophilic amination, and the stereoselective hydroge
34 n and chemically intuitive to assign cations electrophilic and anions nucleophilic reactivity, respec
35 ir molecular analogues because they are less electrophilic and dynamic, as revealed by their (13)C NM
36 depends strongly on the distance between the electrophilic and nucleophilic carbon atoms and the stru
37 droxy groups can be exploited to enable both electrophilic and nucleophilic modes of activation in va
38  complexes with beta-diketiminate ligands in electrophilic and nucleophilic oxidation reactions is re
39 ble to quantitation of other nucleophilic or electrophilic and perhaps even more reactive metabolites
40 l or aryl group; M = a transition metal) are electrophilic and thermally unstable.
41 allenging to identify and study due to their electrophilic and transient nature.
42 w chemical concept of "dipole-discriminating electrophilic anions."
43                        Nitro-fatty acids are electrophilic anti-inflammatory mediators which are gene
44  polycyclic compounds have relied heavily on electrophilic aromatic chemistry, such as the Pictet-Spe
45                                    Classical electrophilic aromatic halogenations are a powerful type
46                             Enantioselective electrophilic aromatic nitration methodology is needed t
47 the rich mechanistic landscape of the iconic electrophilic aromatic substitution (EAS) reaction class
48 eveal two mechanisms for C-H borylation, (i) electrophilic aromatic substitution (prevalent with B-X
49 ort the development of remote regioselective electrophilic aromatic substitution (S(E)Ar) reactions t
50 s was achieved with a highly atroposelective electrophilic aromatic substitution catalyzed by a chira
51 gh the nature of the oxidants that carry out electrophilic aromatic substitution has been deduced fro
52                                              Electrophilic aromatic substitution is one of the most i
53                                          The electrophilic aromatic substitution of a C-H bond of ben
54                 Ability of indole to undergo electrophilic aromatic substitution reaction was studied
55                   Here we perform an abiotic electrophilic aromatic substitution reaction, which is d
56 odel able to predict the reactive site of an electrophilic aromatic substitution with an accuracy of
57 ing cyclization of the E-enone (via Nazarov, electrophilic aromatic substitution, and elimination rea
58       The reaction is thought to proceed via electrophilic aromatic substitution, catalyzed by enzyma
59 the catalytic residue determines the site of electrophilic aromatic substitution.
60 ngement, 6-exo-trig cyclization, and a final electrophilic aromatic substitution.
61  rings can be exploited to precisely control electrophilic aromatic substitutions.
62  an anionic CF(3) group is transferred to an electrophilic aryl group.
63 chemiluminescence (CL) based on the specific electrophilic attack of (*)OH.
64 ssential step in the mechanism that makes an electrophilic attack on the olefin bond possible as the
65 heterolytic cleavage, sigma-bond metathesis, electrophilic attack, etc.
66 ole in activating the olefin for concomitant electrophilic attack.
67 s, iodine(III) salts feature two directional electrophilic axes perpendicular to each other.
68 y an intermolecular C-N bond formation using electrophilic azidoiodinane.
69 igations reveal the intermediacy of a highly electrophilic Bi(V) species, which rapidly eliminates ph
70 rylation of (hetero)arenes and alkenes using electrophilic boranes is a powerful transition metal fre
71 ategy that applies unique features of highly electrophilic boron catalysts, such as tris(pentafluorop
72                                Acyl-directed electrophilic borylation can be extended to carbazoles a
73       Herein, a facile one-pot hydroboration electrophilic borylation cascade/dehydrogenation approac
74 pyridyl ring have been prepared via directed electrophilic borylation.
75      We also show for the first time that an electrophilic borylene such as 1 can react with N2 rever
76 his mechanism and is found to involve double-electrophilic bromination followed by thermal eliminatio
77                            A highly reactive electrophilic bromodifluoromethylthiolating reagent, alp
78 ing between a tertiary carbon radical and an electrophilic butenolide resulting in the stereoselectiv
79 is typically nucleophilic, has been rendered electrophilic by changes to the oxidation state.
80 dented pathway that avoids the production of electrophilic byproducts, a severe limitation that has p
81  with no evidence for attachment at the more electrophilic C(2)-position.
82  undergoes a C-C bond cleavage to produce an electrophilic C-3 site in N-pyridyl indole.
83 zirconia, imbuing high levels of activity in electrophilic C-H bond functionalization reactions such
84 hetic procedures reported for intramolecular electrophilic C-H borylation contain many common feature
85 s, with acyl group installation and directed electrophilic C-H borylation enabling selective formatio
86                      To date, intramolecular electrophilic C-H borylation is utilised mainly for acce
87                Less prevalent intramolecular electrophilic C-H borylation reactions that proceed by i
88 nts are used for sequential nucleophilic and electrophilic C-N bond formations, with the latter effec
89 4+1]-cycloaddition between diazooxindoles as electrophilic C1 synthons and 1,3-heterodienes for the c
90 nation, the pentacyclic core was accessed by electrophilic C19-amide activation and transannular spir
91     We show that despite the presence of the electrophilic carbamoyl chloride function the products s
92  previously demonstrated that stable singlet electrophilic carbenes can behave as metal surrogates in
93 Cl](+) ([4](+) ; Xan=9-xanthylium) where the electrophilic carbenium moiety is juxtaposed with the me
94 mplex that controls the configuration at the electrophilic carbon and a copper catalyst that controls
95 tional reactions, such as methyl transfer to electrophilic carbon atoms, sulfur to Calpha atom thioet
96 he nucleophile prefers to attack at the more electrophilic carbon of the pai-allyl iridium intermedia
97 ave been dicarbofunctionalized here with two electrophilic carbon sources under reductive conditions.
98 ually, ynamides are excellent acceptors for "electrophilic" carbon-centered radicals.
99 ofur is an antineoplastic drug containing an electrophilic carbonyl reactive group that targets the c
100  With the view of developing self-activating electrophilic catalysts, we are now investigating comple
101 relectrophiles that are composed of a strong electrophilic center firmly embedded in a negatively cha
102 bond formation and at a later stage a remote electrophilic center to facilitate OH(-) nucleophilic at
103 inetics, consistent with the presence of two electrophilic centers in NO2-CLA located on the beta- an
104 ch as TiO(2), constitute remarkable powerful electrophilic centers, capable of capturing an electron
105 f Z-type ligands can be used to modulate the electrophilic character and catalytic properties of coor
106                            Most notably, the electrophilic character at the 4-position of pyridine in
107 h molecular orbital analysis, which suggests electrophilic character at the nitride functionality.
108 65e and +0.64e, respectively, indicating the electrophilic character of the phosphinidene {(NHC)C(Ph)
109 gations is the development of catalysts with electrophilic character that transfer electrophilicity t
110  presents a unique challenge for introducing electrophilic chemical groups.
111                    Directed nucleophilic and electrophilic chemistry was developed to vary this 5-pos
112 We report a highly efficient ortho-selective electrophilic chlorination of phenols utilizing a Lewis
113 oate esters via the activation of alkynes by electrophilic chlorine, generated in situ from N-chloros
114 (E=S, Se) dianion, which can be reacted with electrophilic [ClP(mu-NR)]2 to give P(III) /P(V) hexamer
115         MPMN is a bench-stable, carbon-bound electrophilic CN reagent that does not release cyanide u
116 ethod to monitor the metabolic regulation of electrophilic cofactors and discover novel types of elec
117 s are typical hydroxylations, mediated by an electrophilic compound I mechanism.
118                         We further show that electrophilic compounds can impair T cell activation by
119                                              Electrophilic compounds originating from nature or chemi
120 in mass spectrometry to profile specifically electrophilic compounds originating metabolites.
121 and-gated channel, TRPA1 can be activated by electrophilic compounds such as allyl isothiocyanate (AI
122        The TRPA1 ion channel is activated by electrophilic compounds through the covalent modificatio
123  an enzyme that catalyzes the conjugation of electrophilic compounds with glutathione to facilitate t
124 forms covalent bonds between GSH and various electrophilic compounds, through covalent adduct formati
125 s occurs to access a uniquely effective acyl electrophilic coupling partner.
126 ides or pseudohalides were the only suitable electrophilic coupling partners.
127                                Employing the electrophilic cyanating reagent N-cyano-N-phenyl-p-tolue
128  to internally substituted 1,3-dienes and an electrophilic cyanating reagent with high regio and ster
129 nzonitriles from aryl (pseudo)halides and an electrophilic cyanating reagent, 2-methyl-2-phenyl malon
130 organylchalcogenyl)isoquinoline-2-oxides via electrophilic cyclization between alkynylbenzaldoximes a
131 inolines and azido-iodo-pyranoquinolines via electrophilic cyclization of o-alkynylaldehydes in the p
132 lenides and iron(III) chloride, but a direct electrophilic cyclization, promoted by the in situ forme
133 ts new role as an alkynophilic Lewis acid in electrophilic cyclization/dealkylation reactions.
134   The angular methyl groups were attached by electrophilic cyclopropanation-ring opening.
135 propane hydrolase activity that converts the electrophilic cyclopropane of the colibactins into an in
136 NRPS-PKS assembly line and incorporating two electrophilic cyclopropane warheads into the final natur
137 hat colibactin alkylates DNA with an unusual electrophilic cyclopropane.
138 iotic fungal metabolites possessing a masked electrophilic cyclopropane.
139 or 12% of the oxidation products, as well as electrophilic dehydration products of the cholesterol hy
140 sphirene (1) was prepared by treatment of an electrophilic diamidocarbene with tert-butylphosphaalkyn
141 ity toward diacetyl and methylglyoxal, toxic electrophilic dicarbonyls.
142 ion of chlorine gas followed by Cl2-mediated electrophilic dichlorination.
143 n, hydrodehalogenation of halothiophenes, or electrophilic "dimerization".
144 ctive interactions between a nucleophile and electrophilic dye in complex environments is a central g
145                                     However, electrophilic early transition metal (groups 3 and 4)-ca
146                                           An electrophilic enantioselective catalytic method for the
147 t umpolung via N-oxide addition generates an electrophilic enolonium species that can be coupled with
148 bs molecular O(2), forming a rarely reported electrophilic eta(2)-O(2) species at 298 K.
149 ated dienes enable the formation of a highly electrophilic eta(3) Pd-allyl species and greatly facili
150   Herein, the anti-neoplastic effects of the electrophilic fatty acid nitroalkene derivative, 10-nitr
151                                   Endogenous electrophilic fatty acids (EFAs) mediate anti-inflammato
152 l bromides is observed in the presence of an electrophilic fluorinating reagent containing a weak N-F
153 s of alpha-fluoro-beta-ketosulfides using an electrophilic fluorination method has been reported for
154                 The reaction proceeds via an electrophilic fluorination of alpha-sulfenyl-beta-diketo
155   The large majority of known methods employ electrophilic fluorination reagents, but methods combini
156      The main focus has been directed to the electrophilic fluoroalkylation and arylation methods.
157 report the synthesis of a diverse library of electrophilic fragments and demonstrate an integrated us
158 -NRF2 pathway, to discover cysteine-reactive electrophilic fragments from a reporter-based screen for
159 mits reversible fragment screening, but such electrophilic fragments were considered nonselective and
160 enge and constructed a library of 993 mildly electrophilic fragments.
161 ium methylating reagent that preserves other electrophilic functionalities on the substrate.
162 xploited the reactivity of novel unsaturated electrophilic functions such as vinyl-sulfones, -ketones
163  the carbonyl carbon of a peptide bond or an electrophilic group of an inhibitor.
164                                              Electrophilic groups that target amino-acid nucleophiles
165                                              Electrophilic halofunctionalization reactions have under
166 (XB), the noncovalent interaction between an electrophilic halogen atom and a Lewis base, with highly
167 ssically, this reaction is performed with an electrophilic halogen source and leads to regioselective
168 he first concept of copper-catalyst-promoted electrophilic halogenation of carbazoles.
169 al phosphoric acid catalyzed atroposelective electrophilic halogenation of N-aryl quinoids, a class o
170  intrinsic reactivity profile of the method (electrophilic halogenation or C-H borylation) so selecti
171 s reagent IPy2BF4 is used to generate a soft electrophilic halonium species for the iodination of the
172 ons of sodium thiomethoxide (NaSMe) with two electrophilic hemicyanine dyes bearing Btz (1) or Ind (2
173 7) which Fukui analysis shows to proceed via electrophilic insertion of the nitride into the Si-H bon
174 major line of defense to combat oxidative or electrophilic insults.
175 facilitated by an unusual interception of an electrophilic intermediate by water generated via acetat
176  is the first report of hydration through an electrophilic intermediate generated during [3,3]-acylox
177 in a ribosomally synthesized peptide, via an electrophilic intermediate that may be the intended prod
178               An oxidative procedure for the electrophilic iodination of phenols was developed by usi
179   Mechanistic investigations support that an electrophilic iron carbene mediates homolytic C-H cleava
180 e, were investigated in reactions with three electrophilic iron complexes of varying electronic prope
181 ow-threshold sensor for structurally diverse electrophilic irritants, including small volatile enviro
182 tions as a sentinel for structurally diverse electrophilic irritants.
183 opening for selective covalent attachment of electrophilic ligands in eubacterial TGTs.
184               A new study shows that a small electrophilic, lipid-derived molecule protects both land
185 al oxidation of TEMPO-Me produces a powerful electrophilic methylating agent in situ.
186 to directly interrogate how these individual electrophilic modifications at low occupancy functionall
187 philic cofactors and discover novel types of electrophilic modifications on proteins in human cells.
188 r has received clinical approval and several electrophilic modifiers of the cysteine-based sensor KEA
189  main line of cellular defense against these electrophilic molecules is conjugation to glutathione, t
190 d anilines has been developed to generate an electrophilic N-aryl nitrenoid intermediate that can eng
191 ate, radical C-H fluorinations mainly employ electrophilic N-F fluorination reagents but a unique Mn(
192                                          The electrophilic nature of the [B12 Cl11 ](-) anion is conf
193    The success of this pathway is due to the electrophilic nature of the Cp ligand in the cation, [OR
194 termined to be inversely correlated with the electrophilic nature of the sulfimide.
195 in a way that is not obvious considering the electrophilic nature of these activations.
196        This reactivity is facilitated by the electrophilic nature of these open-shell intermediates a
197                        Herein we report that electrophilic nitro-fatty acids (nitro-oleic acid and ni
198 -), and unsaturated fatty acids give rise to electrophilic nitro-fatty acids (NO2 -FAs), such as nitr
199                                 By contrast, electrophilic nitrogen-containing compounds are much rar
200 proved safety profiles compared to the known electrophilic Nrf2 inducers.
201                                         This electrophilic oncometabolite can alter gene activity at
202 to transient allylmetal species that display electrophilic or nucleophilic properties.
203  cyclization, promoted by the in situ formed electrophilic organoselenium species, cannot be ruled ou
204  intermediate to be ambiphilic, acting as an electrophilic oxidant in the initial N-hydroxylation of
205 osts accumulate lipid bodies (LB) containing electrophilic oxidatively truncated (ox-tr) lipids.
206 y of peroxides, including those in which the electrophilic oxygen is formally isobutyl or neopentyl.
207 opropanes using a bis(silyl) peroxide as the electrophilic oxygen source.
208 al that competition between nucleophilic and electrophilic palladium difluorocarbene ([Pd]=CF(2)) is
209  4,7-dihydroindole with aryl-aldehydes as an electrophilic partner followed by an oxidation step to d
210  hydrogen bonding (HB) a nucleophilic and an electrophilic partner form a new bond that is based on a
211                   Considering aryl azides as electrophilic partners for the TosMIC mediated Van Leuse
212  reaction conditions across a broad range of electrophilic partners remains elusive.
213 tion using trifluoroacetimidoyl chlorides as electrophilic partners.
214 ade reactions: those involving nucleophilic, electrophilic, pericyclic, and radical reactions.
215 addition is a classical reaction between the electrophilic phosphinidene and an alkene.
216 of pinacolborane through addition across the electrophilic phosphorus and nucleophilic N-methylanilid
217  most nucleophilic (sigma donating) and also electrophilic (pi-accepting) stable carbenes known to da
218                                 The covalent electrophilic polymerization generates polymers with liv
219 g their superior dienophilic, enophilic, and electrophilic power.
220                         Small-molecule-based electrophilic probes for H(2) O(2) require many minutes
221                                 Unlike other electrophilic probes, the current probe acts as a nucleo
222 he side chains of serine and cysteine, using electrophilic probes.
223  several reaction sites with nucleophilic or electrophilic properties.
224 rgets the same cysteine residue and that our electrophilic quinazolines modulate the function of V-AT
225      The process involves the addition of an electrophilic radical to the electron-rich alkenyl boron
226 re found between the experimentally observed electrophilic reactivities of 44 Michael acceptors and t
227                     In order to quantify the electrophilic reactivities of common Michael acceptors,
228 echanisms and to elucidate the origin of the electrophilic reactivities.
229 the method of choice for a rapid estimate of electrophilic reactivities.
230    Our bioconjugation technique exploits the electrophilic reactivity of an oxidized selenocysteine r
231 rmation, a new mechanism is proposed for the electrophilic reactivity of the phosphaethynolate ion.
232 by transformations relying on their inherent electrophilic reactivity.
233 tion reaction using substrate 2 as a 1,3-bis-electrophilic reagent.
234 roxyl group derivatization with a variety of electrophilic reagents are discussed.
235 heterocycles are easily functionalized using electrophilic reagents, enabling divergent access to var
236 ble and thermodynamically favored through an electrophilic rearrangement and concomitant 1,9-aryl mig
237 In the absence of an external Bronsted base, electrophilic, remote zeta C-H activation takes place, f
238 on of thiiranium ion derivatives became more electrophilic (rho = +1.69; R(2) = 0.974).
239       This study focuses on the formation of electrophilic ring cleavage products-a class of compound
240 verts nucleophilic cysteine residues into an electrophilic S-aryl-Pd-X unit by taking advantage of an
241 tablish a series of synthetically accessible electrophilic scaffolds tunable across multiple centers.
242          This Pd-catalyzed reaction using an electrophilic SCN source offered an efficient tool to ac
243 sition-metal catalyst, instead proceeding by electrophilic selenation or iodination of a vinyl borona
244 action of beta,gamma-unsaturated oximes with electrophilic selenium and tellurium species, affording
245 ustrates the pharmacological utility of this electrophilic series.
246 nge of hydrosilation mechanisms that feature electrophilic silicon centers.
247                          Additionally, other electrophilic silicon species, such as silylene complexe
248 lladium cations to behave as sources of both electrophilic silylium ions and nucleophilic L(n)Pd(0).
249  of a heteroatom nucleophilic site and a pai-electrophilic site.
250 nconventional new platform for incorporating electrophilic sites at remote sp(2) C-H linkages.
251 e use of ES(r), one can identify the various electrophilic sites within a molecule and correctly pred
252 fication of the surface and formation of the electrophilic sites.
253 able cysteines in human T cells and point to electrophilic small molecules as a fertile source for ch
254 d rapid profiling of the cellular targets of electrophilic small molecules.
255 onal sites and can frequently be targeted by electrophilic small molecules.
256  are susceptible to covalent modification by electrophilic small molecules.
257  the targets and signaling roles of reactive electrophilic species (RES) at a specific cellular space
258 d crosstalk choreographed by native reactive electrophilic species (RES).
259  visible light, probably due to formation of electrophilic species such as QMs.
260                                 These highly electrophilic species undergo polarized radical addition
261 gh protonation of an oxo ligand to give more electrophilic species.
262 intermediate as the more plausible transient electrophilic species.
263 te connecting cell metabolism, oxidative and electrophilic stress responses and immune responses.
264 ne of the master regulators of oxidative and electrophilic stress responses.
265 omine (HOBr) was found to react with DOM via electrophilic substitution (</=40%), forming AOBr, and t
266 ct as alkenyl silanes in Hiyama coupling and electrophilic substitution and as dienes in Diels-Alder
267 l NHCs, which show superior stability toward electrophilic substitution and cyclometalation chemistry
268 gated terminal alkyne toward Lewis-activated electrophilic substitution and led to the isolation of F
269 through sequential nucleophilic addition and electrophilic substitution followed by a Mamedov rearran
270                 [B(12)X(11)](-) reacts by an electrophilic substitution of a proton in an alkane resu
271 ns as well as provide new strategies for the electrophilic substitution of aromatic rings.
272                  The chlorination pathway of electrophilic substitution of Cl at the ortho or para po
273 led) by chlorine to HOBr, leading to further electrophilic substitution of unaltered DOM sites and ch
274 in, we report a new approach that allows the electrophilic substitution of YMs.
275                                          The electrophilic substitution reaction of 4,7-dihydroindole
276                             One consisted of electrophilic substitution, whereby the nitrosonium ion
277 acidic and therefore require highly reactive electrophilic substrates to be effective.
278 ion of Cu-H monomer from Cu-H dimer for more electrophilic substrates, and hydride transfer from a tr
279 nsfer from a transient Cu-H monomer for less electrophilic substrates.
280 nantioselective, cyclization of phenols with electrophilic sulfenophthalimides onto isolated or conju
281  difunctionalization of alkenes initiated by electrophilic sulfenyl group transfer.
282                                 A method for electrophilic sulfenylation by organophosphorus-catalyze
283 C)(CO)(m) ](x) (n=5,6; m=15,16; x=0,-2) with electrophilic sulfur sources (S(2) Cl(2) , S(8) ) result
284                             Furthermore, the electrophilic sulfur strategy has been extended to provi
285 n anchors the organometallic proximal to the electrophilic, tetrasubstituted sulfone to override comp
286 ligands render a Mo-alkylidyne a priori more electrophilic than analogous monodentate triarylsilanols
287 ly activating the alkyne, despite being less electrophilic than other known alkyne-activating reagent
288     Lewis base/Bronsted acid cocatalysis for electrophilic thiocyanation of olefins is reported.
289 ic route to convert nucleophilic thiols into electrophilic, thiol-selective vinylphosphonothiolates:
290 rein, we report a ligand-free Cu(I) mediated electrophilic thiolation of organostannanes with sulfur
291  substitution of the heteroaryl halide by an electrophilic thiyl radical, highlighting an underdevelo
292 t, by rendering the alpha-position of amides electrophilic through a mild and chemoselective umpolung
293 hilic substitution, photoredox coupling, and electrophilic transfer reactions allowing the generation
294  relevant conditions via isomerization to an electrophilic vinyl sulfone.
295  surface while simultaneously introducing an electrophilic 'warhead' to covalently react with a nucle
296 xplored di- and tripeptides with beta-lactam electrophilic warheads as inhibitors of dengue and West
297                 Their utility as alternative electrophilic warheads for chemical biological probes an
298 X4-inhibiting molecules have uncovered novel electrophilic warheads that bind and inhibit GPX4.
299 re equal in terms of their reactivity toward electrophilic warheads.
300 inding ligands with appropriately positioned electrophilic warheads.

 
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