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1 ese TMP salts were demonstrated to be highly chemoselective.
2 te experimental data showing that it is less chemoselective.
3 al environments and then undergo a rapid and chemoselective 1,4-Michael addition with the pKa-perturb
4                            Additionally, the chemoselective 1,4-reduction of the enone products provi
5               Furthermore, this allows for a chemoselective 1,5-HAT over competing direct cyclization
6                           This has enabled a chemoselective 1,6-HAT over a competing 1,5-HAT.
7 oxazolidinone-substituted oxyallyl undergoes chemoselective (3 + 2) cycloaddition onto the carbonyl g
8 n with photoredox catalysis allows for mild, chemoselective access to a wide array of related structu
9          Driven by the unmet need to develop chemoselective access to boron chemotypes, we report her
10                                          The chemoselective acetoxylation of the epsilon-C-H bond was
11                    Especially, the BDG-aided chemoselective acetoxylation of the remote epsilon-C(sp(
12 -catalyzed, bidentate directing group-aided, chemoselective acetoxylation/substitution of remote epsi
13                                              Chemoselective acidic hydrolysis of sulfonamides with tr
14                                          The chemoselective activation and coupling of C-terminal pep
15                                              Chemoselective activation of amide carbonyl functionalit
16 ysis has emerged as a powerful technique for chemoselective activation of chemical bonds under mild r
17 -amino acid selenoesters which are effective chemoselective acylating reagents.
18 etic derivatization of starting material via chemoselective acylation of the l-ornithine alpha-amino
19 th microscopic investigation that probes the chemoselective addition of Ag to Pt-Fe3O4 heterodimer se
20                                          The chemoselective addition of arenes and 1,3-diketones to a
21 a'-haloketones has been achieved through the chemoselective addition of halomethyllithium carbenoids
22                                          The chemoselective addition of N-heterocycle 1a onto alkyne
23 inert atmospheres in toxic organic solvents, chemoselective addition of organolithium reagents to non
24                                       Highly chemoselective addition of Schwartz's reagent to widely
25      An efficient organocatalytic method for chemoselective aerobic oxidation of secondary benzylic a
26                                The method is chemoselective against secondary and primary alcohols, t
27  a non-natural amino acid (NNAA) followed by chemoselective albumin conjugation to prolong therapeuti
28 tion that normally poses major challenges in chemoselective, aliphatic C-H functionalization.
29 es by a pyridinium dichromate (PDC)-mediated chemoselective allylic oxidation.
30 amily of iron catalysts capable of promoting chemoselective alpha-oxidation of a range of ethers with
31                                     Notably, chemoselective amidation of aliphatic amines takes place
32 (Asa) side chain can be easily prepared by a chemoselective amide-forming ligation that results in th
33                                 We show that chemoselective amide-forming ligations of potassium acyl
34 talysts capable of promoting predictable and chemoselective aminations solely through reagent control
35                 Herein, we report remarkable chemoselective aminations that employ a single metal (Ag
36  C, and D, through a route fueled by several chemoselective and carefully orchestrated steps.
37 y Z-selective alkene cross-metathesis, and a chemoselective and diastereoselective dichlorination of
38 lar nitrene transfer reactions that are both chemoselective and flexible for aziridination or C-H ins
39 s fast, operationally simple, high yielding, chemoselective and functional group tolerant method.
40                            The reactions are chemoselective and high yielding.
41 h repeat unit, which is enabled by perfectly chemoselective and highly syndiospecific coordination po
42 e-reduction methods, this reaction is highly chemoselective and is compatible with alcohols, phenols,
43                                     Multiple chemoselective and redox-economic functional group inter
44 proach outlined in this protocol enables the chemoselective and regioselective late-stage silylation
45 udo-single-atom structures as highly active, chemoselective and reusable catalysts for hydrogenation
46 that peptide fragments can be exchanged by a chemoselective and reversible native chemical ligation (
47 yne substrates are found to undergo a highly chemoselective and stereoselective domino Pauson-Khand a
48 ty of this catalyst system is evident in the chemoselective and stereospecific oxidation of the polyo
49                         The reaction is both chemoselective and syn-selective, making it complementar
50                                The method is chemoselective and tolerates a wide range of reducible f
51 igosaccharide synthesis including selective, chemoselective, and orthogonal strategies is demonstrate
52                   The reaction is efficient, chemoselective, and pH/redox neutral.
53 mer-polymer click reaction, achieving rapid, chemoselective, and quantitative coupling at room temper
54             This mild, operationally simple, chemoselective, and scalable difluoromethylation method
55        Discovery of this broadly applicable, chemoselective, and solvent-versatile reagent should all
56 gy involves low catalyst loadings, is highly chemoselective, and tolerates a wide variety of function
57 techol-boronate binding mechanism provides a chemoselective approach for controlling the release of B
58                                            A chemoselective approach was developed for the synthesis
59 d, among them the most recent strategies for chemoselective arene metalation on peptides.
60 useful toolkit of Cu-based catalysts for the chemoselective arylation of a wide-range of nucleophiles
61 clamp motif (Phe-Cys-Pro-Phe) for regio- and chemoselective arylation of cysteine in ribosomally prod
62                                     Notably, chemoselective arylation of diazo compounds over other e
63                         The method is highly chemoselective as a vast array of functional groups are
64 Reformatsky reactions as a powerful tool for chemoselective asymmetric carbon-carbon bond formations,
65                             The procedure is chemoselective, avoids the use of precious metals, and c
66 al C-H abstraction/rebound, as observed with chemoselective base metals such as iron.
67  lignin degradation strategy consisting of a chemoselective benzylic oxidation with a recyclable oxid
68 er as a mechanism towards enabling site- and chemoselective bioconjugation.
69 further method development in the context of chemoselective, bioorthogonal labeling.
70                  The identification of fast, chemoselective bond-forming reactions is one of the majo
71  for a range of organic reactions, including chemoselective borylation, silylation and amination of b
72                Also, Ag-mediated, completely chemoselective Br displacement from 2S leads to a range
73                     This reaction allows the chemoselective C-C bond formation between the pyrrole C3
74                                       Highly chemoselective C-S cross-coupling was achieved versus co
75 el gold surface in regards to NO2 reduction, chemoselective C=O bond hydrogenation, ether formation,
76 f an entropic chemical ligation consist of a chemoselective capture step merging the N and C termini
77                                         This chemoselective carbene insertion into -NH bond over -COO
78  Relying on these factors, highly regio- and chemoselective carbene insertion reaction of C-H bonds i
79 to Dha, promoted by zinc and copper, enables chemoselective carbon-carbon bond formation.
80 trate the application of these catalysts for chemoselective carbon-halogen bond activation to achieve
81                          Palladium-catalyzed chemoselective carbonylation of aminophenols with iodoar
82           Disclosed is a mild, scalable, and chemoselective catalytic cross-dehydrogenative C-H bond
83                                            A chemoselective catalytic fluorination of alkyl triflates
84                                              Chemoselective catalytic oxidation of beta-O-4 linkages
85                      The reaction provides a chemoselective catalytic synthesis of 2H-indazoles, 2H-b
86                      The reaction provides a chemoselective catalytic synthesis of alpha-acyloxy este
87                      Here we report a highly chemoselective catalytic system for the indole oxidation
88  and stable cell-cell contacts in 3D through chemoselective cell-surface engineering based on liposom
89 ere labeled or immobilized by application of chemoselective chemistry at the anomeric center.
90 by chlorotrimethysilane is described for the chemoselective chlorination of polyprenoids.
91                                              Chemoselective cleavage of the Phen group was performed
92                                   A stepwise chemoselective click reaction was performed on nucleosid
93 for the synthesis of alkylated arenes by the chemoselective combination of two electrophilic carbons.
94 g molecules is also affected by geometry and chemoselective confinement via matrix binding.
95 issue assemblies through chemistry involving chemoselective conjugation and release.
96 licylate as a novel molecular switch for the chemoselective construction of the macrodiolide.
97 hydroxy ketone to a diketone was followed by chemoselective conversion of the methyl ketone in this s
98 alized cyclopentenones can be generated by a chemoselective copper(II)-mediated Nazarov/Wagner-Meerwe
99  the less reactive allylphenyl carbonates as chemoselective copper-hydride elimination is faster with
100  antero- and retrograde tracers in rats, and chemoselective, Cre-dependent viral constructs in parval
101 riazolium salts are shown to catalyze highly chemoselective cross-benzoin reactions between aliphatic
102 n iridium-catalyzed Krische allylation and a chemoselective cross-coupling approach toward the macroc
103  alpha,beta-unsaturated carbonyl compound by chemoselective cross-coupling of propargyl alcohols with
104 SCl, and a mild reductant can participate in chemoselective cross-coupling with aryl iodides using a
105 neous electrophile control allows sequential chemoselective cross-couplings in a single operation in
106        An efficient protocol for stereo- and chemoselective crystallization of (S)-1,2-dodecanediol a
107 on of primary alcohols to aldehydes, using a chemoselective Cu(I)/TEMPO (TEMPO = 2,2,6,6-tetramethyl-
108 systems and provides a unifying strategy for chemoselective CuAAC ligations in multialkyne/azide syst
109 ional design of carbonylacrylic reagents for chemoselective cysteine bioconjugation.
110  offer the greatest potential for regio- and chemoselective dehydrogenation of alkyl groups and alkan
111 ex catalyzes oxidant-free, acceptorless, and chemoselective dehydrogenation of primary and secondary
112                          By using the highly chemoselective depolymerization to prepare new ultra low
113                        A new, fast, mild and chemoselective deprotection method to cleave p-methoxybe
114 -irciniastatin A intermediate to implement a chemoselective deprotection/oxidation sequence to access
115                          We have synthesized chemoselective derivatives of the tarantula toxin guangx
116 n of interest in the first step, followed by chemoselective derivatization with a tetrazine-fluoropho
117                                       Highly chemoselective direct reduction of primary, secondary, a
118 f an activating Weinreb carboxamide, further chemoselective elaboration leads to the efficient format
119 Ps, the PRO-functionalized Pt NPs are highly chemoselective even at 100% conversion.
120 uinolinones, and quinolinols in a regio- and chemoselective fashion.
121 azole rings were formed in both a regio- and chemoselective fashion.
122 (OTf)2), N-fluoro-2-methylbenzamides undergo chemoselective fluorine transfer to provide the correspo
123         The polymerization by 1 is perfectly chemoselective for all four polar divinyl monomers, proc
124                        The reaction is fully chemoselective for amides even in the presence of esters
125                             This reaction is chemoselective for aromatic aldehydes, as an aliphatic a
126 port a new iridium catalyst that is strictly chemoselective for C-H borylation of terminal alkynes.
127            The method was shown to be highly chemoselective for cysteine over other potentially nucle
128 s onto diblock-copolymer-coated surfaces are chemoselective for the placement of thiol and alcohol nu
129           The key sequence features a highly chemoselective formamide activation that triggered a Vil
130 e Hg complex that drives the reaction to the chemoselective formation of 2,5-dihydrofurans.
131      Rhodium(I) and a new SDP ligand promote chemoselective formation of a cyclohex-3-enecarbaldehyde
132 inetic effects of DMSO provide the basis for chemoselective formation of cyclohexenones.
133 e addition and transmetalation, this enables chemoselective formation of two C-C bonds in a single op
134  to the assay is the utilization of a highly chemoselective Friedlander reaction that captures and si
135                    Cell surface tailoring of chemoselective functional groups was achieved by a lipos
136 ron products is demonstrated through several chemoselective functionalizations.
137 ive functional group, the reaction is highly chemoselective giving the dichloromethyl derivative.
138                   Applications of 2S include chemoselective Grignard coupling, enabling the very shor
139                                              Chemoselective GxTX mutants conjugated to dendrimeric be
140        Exceedingly facile (23 degrees C) and chemoselective H-CF3 activation with [(dppp)Pd(Ph)(OH)]
141      The stability of the borate unit allows chemoselective halogenation of the heteroaromatic ring,
142                                     A highly chemoselective heteroannulation protocol for the synthes
143 ][HBPh3], act as efficient catalysts for the chemoselective hydroboration of a wide range of aldehyde
144 r work up, 1 degrees and 2 degrees alcohols; chemoselective hydroboration of aldehydes over ketones i
145 droboration of styrenes as well as excellent chemoselective hydroboration of ketones over alkenes wer
146                                              Chemoselective hydroboration of nitriles over esters is
147 e consists of a C3 extension (allylation), a chemoselective hydroboration, an alkyne reduction, and a
148 ization/proto-desilylation sequence; and the chemoselective hydrogenation of a fully substituted dien
149 rity affords a flexible means to control the chemoselective hydrogenation of aromatic aldehydes.
150  remarkably prohibited the hydrogenolysis in chemoselective hydrogenation of C=C bonds, leading to an
151 nanoclusters were utilized as a catalyst for chemoselective hydrogenation of nitrobenzaldehyde to nit
152 C-enabled tunable heterogeneous catalyst for chemoselective hydrogenation.
153                                              Chemoselective hydrolysis of the resulting 5,6-dihydro-1
154                          A copper-catalyzed, chemoselective hydrometalation process enables the use o
155 mbination was explored to achieve regio- and chemoselective hydroxylation.
156                          Using these probes, chemoselective imaging of either H(2)O(2) or caspase 8 a
157 ulfamidate 17 and alcohol 4 and a remarkably chemoselective, improved palladium(II)-mediated Corey-Yu
158                                              Chemoselective interaction of aromatic enynes with Bu3Sn
159                A transprotection tactic by a chemoselective intramolecular 6-exo-trig iodoetherificat
160                                       Highly chemoselective intramolecular amination of propargylic C
161 odides in the presence of Mn2(CO)10 leads to chemoselective iodine atom abstraction and radical addit
162 ble indole-linked delta-lactams via a highly chemoselective iridium(I)-catalyzed reduction.
163 dendralene) and a new method for stereo- and chemoselective isocyanation.
164 hanced resolution and sensitivity offered by chemoselective isotope tags have enabled new and enhance
165 ess the pendant cyclopentenone, and a highly chemoselective lactam reduction delivered the natural pr
166 h native chemical ligation (NCL) and related chemoselective ligation approaches provide an elegant me
167                  Diversification of existing chemoselective ligations is required to efficiently acce
168                        Key steps include the chemoselective lithiation of a 1-iodo-2-bromoolefin, the
169 midazolidinone, which is followed first by a chemoselective malonate PMB ester removal and then a Cur
170 gnized as valuable synthetic handles for the chemoselective manipulation of peptides and proteins.
171 ion, the functionalized end groups allow for chemoselective manipulations and further elongation of t
172  cyclopropenes occur in a regioselective and chemoselective manner to produce either vinyl thioethers
173 amine linkages (secondary and tertiary) in a chemoselective manner under mild, biocompatible conditio
174 onalize the aromatic aminobenzoic acids in a chemoselective manner without implementing protection an
175 achieve patterned bioconjugation in a highly chemoselective manner.
176 The mechanism of a recently reported, highly chemoselective metal-free protocol of wide general appli
177 kyl peroxides with carbanions, generated via chemoselective metal-heteroatom exchange or deprotonatio
178               Here, we report a strategy for chemoselective methionine bioconjugation through redox r
179                                  This highly chemoselective method can tolerate labile and reactive c
180 proach takes advantage of a nonenzymatic and chemoselective method to rapidly generate A2AR embedded
181                          A non-enzymatic and chemoselective method to spontaneously generate phosphol
182 he present methodology provides an efficient chemoselective method to synthesize a variety of (Z)-ena
183          Here, we report a non-enzymatic and chemoselective methodology capable of autocatalytically
184 ires the development of a regioselective and chemoselective methodology.
185 acilitated greatly by recent developments in chemoselective methods for biomolecular modification.
186                      A suite of flexible and chemoselective methods for the transition-metal-free oxi
187                            Non-enzymatic and chemoselective methods to generate phospholipid membrane
188     A novel, organobase-catalyzed and highly chemoselective Michael-Michael-acetalization cascade is
189  catechols with aniline functional groups is chemoselective, mild, and rapid; however, the oxidativel
190 e soft-N-donors as effective complexants for chemoselective minor actinide extraction from used nucle
191 stic orthogonal recoding of translation with chemoselective modification (SORT-M) to address this cha
192 ting-group-free synthesis we demonstrate the chemoselective modification of 12 complex molecules that
193                                              Chemoselective modification of complex biomolecules has
194                                     However, chemoselective modification of the identical functional
195 ilability of a suitable functional group for chemoselective modification.
196 face syn to the ammonium moiety exclusively; chemoselective N-benzylation then provided either (1RS,2
197 d decarbonylative Heck reaction of amides by chemoselective N-C activation using N-acylsaccharins as
198 eck reaction of amides proceeding via highly chemoselective N-CO cleavage catalyzed by Pd(0) utilizin
199                                   Subsequent chemoselective N2'-functionalization and O3'-phosphityla
200                                              Chemoselective nanoporous membranes: tunably porous memb
201 ted peptide segments using site-specific and chemoselective native peptide ligation methods.
202  theory (DFT) was used to explore the highly chemoselective nature of the catalytic hydrogenation of
203                          The predictable and chemoselective nature of these transformations has led t
204 mino ketones with an aza-glycine equivalent, chemoselective nitrogen functionalization, and ring clos
205                                     Mild and chemoselective opening of lactones with sodium trimethyl
206 ectroscopic and kinetic studies suggest that chemoselective organic transformations occur on site-iso
207                        The highly regio- and chemoselective oxidation of activated C-H bonds has been
208                           Unusual regio- and chemoselective oxidation of aromatic amines hindered wit
209 ion conditions employed here is suitable for chemoselective oxidation of secondary alcohol in the pre
210  RuCl3-NaIO4 reagent system were crucial for chemoselective oxidation of sulfide in the presence of a
211                               The regio- and chemoselective oxidation of unprotected vicinal polyols
212 sopropenyllithium TMEDA complex and a facile chemoselective oxidation with selenium dioxide.
213                                          The chemoselective oxidations of akuammicine leading up to t
214 lectively produces the heterocycles based on chemoselective oxidative addition.
215 ble bonds have been exploited to demonstrate chemoselective oxidative cleavage in substrates containi
216                                            A chemoselective oxidative cleavage of synthetic gracilioe
217                              The reaction is chemoselective, oxidizing one alkene in the presence of
218 ross-couplings compared to halides, enabling chemoselective palladium- and nickel-catalyzed coupling
219                        Here, we describe the chemoselective partial reduction of silyl-protected C6O6
220        The chiral dienediynes undergo highly chemoselective Pauson-Khand (PK) cycloaddition in benzal
221 odified Hantzsch pyridine construction and a chemoselective Peng deprotection of a phenolic MOM ether
222         In this Communication, we develope a chemoselective photoacoustic sensor (LP-hCy7) composed o
223       In the present study, we used a unique chemoselective photoaffinity labeling strategy, the meth
224                                      A novel chemoselective polymerization control yields predictable
225                                 An efficient chemoselective practical route to fully substituted thia
226 ronically challenging substrates in a highly chemoselective, practical, and rapid manner.
227  boron atom of the boronic acids, leading to chemoselective primary amination.
228 c reactive handle on the NP is targeted by a chemoselective probe to enable its detection by mass spe
229 obtained from readily available amides via a chemoselective process involving Tf2O-mediated amide cyc
230 itroso compounds has been transformed into a chemoselective process that converts sulfinic acid into
231 tryptophan residue was shown to allow rapid, chemoselective protein modification using the azo-coupli
232 e recent progress made in the development of chemoselective protocols for amide reduction and gives a
233 allography and mass spectrometry confirmed a chemoselective reaction between the sulfonyl fluoride an
234                The results suggest that this chemoselective reaction can occur in the presence of exc
235                                          The chemoselective reaction of donor/acceptor (D/A) and acce
236                     We report the facile and chemoselective reaction of tyrosine-containing G-protein
237  to a given protein and then undergo a rapid chemoselective reaction to form a covalent conjugate hav
238                                 In addition, chemoselective reactions are possible when there are phe
239                Here, we show that reversible chemoselective reactions can be harnessed to achieve non
240                                              Chemoselective reactions for amide bond formation have t
241  of our group's recent advances in exploring chemoselective reactions for stitching together lipid fr
242 e various functional groups, allowing highly chemoselective reactions in the presence of halide, este
243                                    Combining chemoselective reactions with encoded amino acids has fa
244  of the past two decades, the demand for new chemoselective reactions with unique abilities, and thos
245 ehyde capture ligation that parlays the high chemoselective reactivity of aldehydes and amines to enf
246 y dramatic spectral shifts by leveraging the chemoselective reactivity of novel functional groups ins
247 aryl fluorosulfates studied thus far exhibit chemoselective reactivity toward Lys and, particularly,
248 fold to produce protein-like structures with chemoselective reactivity.
249 ast reaction rate with stable, nontoxic, and chemoselective reagents.
250 3-aminophenylboronic acid (FITC-APBA) as the chemoselective recognition probe of sialylation product,
251 ssing the power of high stereo-, regio-, and chemoselective redox biocatalysts and enabling reactions
252                                              Chemoselective reduction and functionalization of these
253 ical transformations were required to permit chemoselective reduction and oxidation reactions.
254 ned pendant hydroxyl group to facilitate the chemoselective reduction of an extremely unreactive lact
255                                              Chemoselective reduction of an intermediate enone requir
256 NHPtBu2] is the first efficient catalyst for chemoselective reduction of challenging unsaturated este
257 werful single electron donors for the highly chemoselective reduction of common functional groups.
258                                              Chemoselective reduction of nitro groups in the presence
259    The protocol exploits the mild and highly chemoselective reduction of the amide and lactam functio
260                         Herein we report the chemoselective reduction of the carbonyl functionality v
261                                Unprecedented chemoselective reductions of phosphine oxides to phosphi
262                  Stannous chloride catalyzed chemoselective reductive amination of a variety of carbo
263  thus formed to react with enals in a highly chemoselective, regioselective, diastereoselective and e
264                                         This chemoselective relay cyclization strategy was utilized i
265            Reported herein is an exceptional chemoselective ring-opening/C(sp(3) )-C(sp(3) ) bond for
266             An eight-sensor array coupling a chemoselective room-temperature ionic liquid (RTIL) with
267                             An efficient and chemoselective route for transforming BF2-BODIPYs to Et2
268                     Herein, we demonstrate a chemoselective, salicylideneanilines-based COF (SA-COF),
269 tial of soft-Lewis basic complexants for the chemoselective separation of trivalent actinides from la
270 mponent catalytic process that begins with a chemoselective, site-selective and diastereoselective co
271                                        These chemoselective solutions should have value to other prob
272 approach relies on the use of two successive chemoselective steps: (i) phosphoramidite coupling, and
273          This contribution reports the first chemoselective, stereospecific, and living polymerizatio
274                     We previously reported a chemoselective strategy for enrichment of hydroxyl-funct
275                                              Chemoselective Suzuki-Miyaura cross-coupling generally r
276 c substituent on the benzylic carbon atom, a chemoselective switch was observed, which preferred intr
277           An efficient, metal and base-free, chemoselective synthesis of aryl-, heteroaryl-, and alky
278                                     A highly chemoselective synthesis of beta-ketophosphonates from p
279 ation is presented as a new strategy for the chemoselective synthesis of boronic esters.
280 lished for [Pd(cinnamyl)Cl](2)/L1 toward the chemoselective synthesis of di-, tri-, and tetraamines w
281         An efficient tandem approach for the chemoselective synthesis of functionalized azido-pyranoq
282         This manuscript describes a one-pot, chemoselective synthesis of three 2,7-diaminosuberic aci
283 y enolsilanes with dienes provide a mild and chemoselective synthetic route to seven-membered carbocy
284 s aim to provide site-specific approaches by chemoselective targeting of canonical and noncanonical a
285 hio)-4-functionalized thiazoles via one-step chemoselective thionation-cyclization of highly function
286 ect synthesis of beta-Mannich products via a chemoselective three-component coupling of aryl aldehyde
287                                          The chemoselective transformation into these functional grou
288 ed amines can easily be accessed in a highly chemoselective transformation.
289        New applications in highly regio- and chemoselective transformations in short reaction times a
290 or the development of a broad range of novel chemoselective transformations via open-shell electron p
291                        A range of successful chemoselective transformations were investigated, which
292 ha-diimine nickel catalysts that promote the chemoselective triborylation of benzylic C(sp(3))-H bond
293                Our work establishes a unique chemoselective "unclickable" bioconjugation strategy to
294                             In addition, the chemoselective use of C-C and C-O pi-bond functionality,
295                   The latter was found to be chemoselective using platinum(IV) oxide as the catalyst
296            Reversible as well as stereo- and chemoselective: various proteases such as thermolysin an
297 and APC-2, a water-soluble congener) for the chemoselective visualization of Cu(II), a metal ion whic
298 s observed, including E/Z isomerizations and chemoselective Wagner-Meerwein shifts.
299 , which is less electrophilic and hence more chemoselective when reacting with nucleophiles.
300                  This method is scalable and chemoselective with broad functional-group tolerance.

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