ライフサイエンスコーパス: cross-coupling reaction

1 , has been established in the Suzuki-Miyaura cross-coupling reaction.

2 alation step required for the Suzuki-Miyaura cross-coupling reaction.

3 unctionality was accomplished by Sonogashira cross-coupling reaction.

4 ydro-2H-pyrans as substrate in a Kumada-type cross-coupling reaction.

5 equent conventional Pd-catalyzed coupling or cross-coupling reaction.

6 synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction.

7 idine ligands were synthesized by the Suzuki cross-coupling reaction.

8 sides were synthesized using the Sonogashira cross-coupling reaction.

9 a versatile catalyst for the Suzuki-Miyaura cross-coupling reaction.

10 ytic efficiency and the base employed in the cross-coupling reaction.

11 l esters and amides through a Suzuki-Miyaura cross-coupling reaction.

12 nistic underpinnings to a photocatalytic C-N cross-coupling reaction.

13 s of the palladium-catalyzed decarboxylative cross-coupling reaction.

14 nces the quantum yield and efficiency of the cross-coupling reaction.

15 nd (e.g., BIDIME) was reported in the Suzuki cross-coupling reaction.

16 lysis to predict the regioselectivity of the cross-coupling reaction.

17 hexagons, by means of a palladium-catalyzed cross-coupling reaction.

18 e MCF-7 lineage as an efficient catalyst for cross-coupling reaction.

19 ioethers via a Ni-catalyzed stereoconvergent cross-coupling reaction.

20 rins were synthesized through Suzuki-Miyaura cross coupling reactions.

21 e proposed key intermediates in Cu-catalyzed cross-coupling reactions.

22 w turnover numbers relative to non-oxidative cross-coupling reactions.

23 ve to traditional transition-metal-catalysed cross-coupling reactions.

24 ng complementary choices for further various cross-coupling reactions.

25 are particularly valuable in metal-catalyzed cross-coupling reactions.

26 the transmetalation step in Pd/Cu-catalyzed cross-coupling reactions.

27 olithium reagents in the palladium-catalyzed cross-coupling reactions.

28 t the stereochemical outcome of Pd-catalysed cross-coupling reactions.

29 nucleophiles in stereospecific, Pd-catalysed cross-coupling reactions.

30 abundance, and its ability to promote unique cross-coupling reactions.

31 ortant yet elusive objective for engineering cross-coupling reactions.

32 only proposed as the active intermediates in cross-coupling reactions.

33 lkyl groups to transition metal catalysts in cross-coupling reactions.

34 their impact on the stereochemical course of cross-coupling reactions.

35 nate can serve to direct palladium-catalyzed cross-coupling reactions.

36 of challenging C-C and C-X (X = heteroatom) cross-coupling reactions.

37 ign in facilitating challenging Pd-catalyzed cross-coupling reactions.

38 h electrophiles as well as Stille and Suzuki cross-coupling reactions.

39 idant-free Au(I)-catalyzed carbon-heteroatom cross-coupling reactions.

40 g, Suzuki-Miyaura, and metallophotoredox C-N cross-coupling reactions.

41 ials in the Suzuki, Sonogashira, and Ullmann cross-coupling reactions.

42 o competent catalysts for Kumada and Negishi cross-coupling reactions.

43 onstrated by applying it to literature known cross-coupling reactions.

44 synthesis, but have rarely been employed in cross-coupling reactions.

45 d several intermediates were seen in Negishi cross-coupling reactions.

46 e highly effective in Suzuki-Miyaura and C-N cross-coupling reactions.

47 ally prepared through kinetically controlled cross-coupling reactions.

48 of the heterocyclic ring via Suzuki-Miyaura cross-coupling reactions.

49 es a well-defined pincer-Rh catalyst for C-S cross-coupling reactions.

50 ts for metal-free formal C(sp(2) )-C(sp(2) ) cross-coupling reactions.

51 es high catalytic activity for carbon-sulfur cross-coupling reactions.

52 use of organo-halide reagents in traditional cross-coupling reactions.

53 ed from the precursor iodide 7 using Negishi cross-coupling reactions.

54 method to use secondary alkyltin reagents in cross-coupling reactions.

55 atalytic performance in an eclectic array of cross-coupling reactions.

56 bility and poor reactivity in Suzuki-Miyaura cross-coupling reactions.

57 nds as substrates for Suzuki and Sonogashira cross-coupling reactions.

58 ution and through transition-metal-catalyzed cross-coupling reactions.

59 visible light photoredox catalysts for aryl cross-coupling reactions.

60 nvolving two consecutive palladium-catalyzed cross-coupling reactions.

61 e precursors prepared by palladium-catalyzed cross-coupling reactions.

62 s the range of reagents available for N-C(O) cross-coupling reactions.

63 e scope of Ni-catalyzed reductive asymmetric cross-coupling reactions.

64 (CMPs) synthesized by Buchwald-Hartwig (BH) cross-coupling reactions.

65 nd alkynyl groups, in excellent yields using cross-coupling reactions.

66 ituent at the 3-position and Pd(0)-catalyzed cross-coupling reactions.

67 ovel approach to facilitate nickel-catalyzed cross-coupling reactions.

68 anding catalytic activity for Suzuki-Miyaura cross-coupling reactions.

69 are challenging targets for metal-catalyzed cross-coupling reactions.

70 limitations of iron-catalyzed Kumada-Corriu cross-coupling reactions.

71 echanisms in the growing class of HAT alkene cross-coupling reactions.

72 : 1) Palladium-nanoparticle-catalyzed Suzuki cross-coupling reactions, 2) palladium- or silver-nanopa

73 of anomeric configuration make the glycosyl cross-coupling reaction a practical tool for the synthes

74 ting the performance of a photocatalytic C-N cross-coupling reaction across multiple reactor sizes an

75 oducing biocatalysts with a Buchwald-Hartwig cross-coupling reaction, affording a variety of alpha-ch

76 al Cu-catalyzed stereocontrolled sp(3)-sp(3) cross-coupling reactions allowed convergent assembly of

77 In Pd-catalyzed C-N cross-coupling reactions, alpha-branched secondary amine

78 synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction and subsequent [2 + 2] cycloaddi

79 detailed mechanistic study of the aziridine cross-coupling reaction and the role of EDO ligands in f

80 ic alkylation expands the synthetic scope of cross-coupling reactions and can be further extended to

81 implications for the design of N-C(O) amide cross-coupling reactions and control of the molecular co

82 ladium nanoparticle-catalyzed Suzuki-Miyaura cross-coupling reactions and evaluated as human carbonic

83 rth-abundant" transition-metal catalysts for cross-coupling reactions and extraction and fractional c

84 ves through conventional palladium-catalyzed cross-coupling reactions and iodine-lithium exchange pro

85 t into the overall mechanism of Ni-catalyzed cross-coupling reactions and offers a basis for differen

86 lvement of organometallic Ni(III) species in cross-coupling reactions and oxidatively induced C-heter

87 derstanding the mechanisms of iron-catalyzed cross-coupling reactions and rational design of novel ir

88 The heteroarylsilane products undergo cross-coupling reactions and substitution reactions with

89 reaction, a palladium-catalyzed Stille-Kelly cross coupling reaction, and a carbon monoxide-mediated

90 ing Boc and Cbz groups are stable to further cross coupling reactions, and readily deprotected.

91 s alkynyl protecting groups, (2) Sonogashira cross-coupling reactions, and (3) the development of rin

92 nthetic transformations, including iterative cross-coupling reactions, and a Chan-Lam-type allyloxyla

93 (1) was prepared via two consecutive Suzuki cross-coupling reactions, and the three-dimensional stru

94 exert electric-field effects on the rate of cross-coupling reactions, and their cocatalytic effects

95 of transmetalation in aqueous Suzuki-Miyaura cross-coupling reaction are discussed.

96 talyzed C(sp)-C(sp(2)) and C(sp(2))-C(sp(2)) cross-coupling reactions are accomplished with aryldiazo

97 Nickel-catalyzed cross-coupling reactions are experiencing a dramatic res

98 Transition metal-catalysed cross-coupling reactions are widely used for constructio

99 Using palladium-catalyzed cross-coupling reactions as a test case, we developed au

100 arbon-halogen bond activation to achieve C-C cross-coupling reactions as well as reductive dehalogena

101 s been accomplished using the Suzuki-Miyaura cross-coupling reaction at or near physiological tempera

102 Its nucleophilic substitutions or cross-coupling reactions at position 8 and deprotection

103 In cross-coupling reactions, azobenzenes therefore usually

104 report a series of enantioselective C-O bond cross-coupling reactions based on remote symmetry breaki

105 The Buchwald-Hartwig cross-coupling reaction between 4-methylumbelliferone-de

106 Capitalizing on the Pd-catalyzed Suzuki cross-coupling reaction between a tris-triflate borazine

107 a copper-catalyzed domino Michael/oxidative cross-coupling reaction between adenines and nitroolefin

108 asymmetric iron-catalyzed C(sp(2))-C(sp(3)) cross-coupling reaction between Grignard reagents and al

109 erated through a palladium-catalyzed Ullmann cross-coupling reaction between o-iodonitrobenzene and a

110 The selective FeCl(3)-catalyzed oxidative cross-coupling reaction between phenols and primary, sec

111 estigation of the palladium-catalyzed Kumada cross-coupling reaction between PhMgBr and (pseudo-ortho

112 prepared using a palladium-catalyzed Ullmann cross-coupling reaction between the appropriate 2-iodocy

113 is a mild, scalable, visible-light-promoted cross-coupling reaction between thiols and aryl halides

114 Cross-coupling reaction between two C-H bonds has become

115 Suzuki-Miyaura cross-coupling reactions between a variety of alkyl hali

116 atalyst capable of promoting carbon-nitrogen cross-coupling reactions between a variety of primary am

117 s and have also been employed as partners in cross-coupling reactions between aromatic, alkenyl, alky

118 Csp(2)-Csp(2) cross-coupling reactions between arylboronic acid and ar

119 ss spectra suggests that there are extensive cross-coupling reactions between hydroxy-carbonyl produc

120 Selected examples of C-N cross-coupling reactions between nine classes of nitroge

121 Transition metal-catalyzed cross-coupling reactions between organic electrophiles a

122 ting group, which otherwise does not allow a cross-coupling reaction, by transformation to the N-oxid

123 c transformations such as the Suzuki-Miyaura cross-coupling reaction, C-H bond activation, dehydrogen

124 ized aryl iodides are introduced, subsequent cross coupling reactions can be used for further modific

125 A highly chemoselective phenol cross-coupling reaction catalyzed by a Cr-salen catalyst

126 A sp(3)-sp(2) C-C cross-coupling reaction catalyzed by gold in the absence

127 ingle kinetically relevant step in different cross-coupling reactions catalyzed by sub-nanometer Pt o

128 fective room-temperature palladium-catalyzed cross-coupling reactions (CCRs) of aryl and heteroaryl c

129 a directing group for C(sp(2))-H activation/cross-coupling reactions, circumventing the extra steps

130 o-metabolites, develop a mild Suzuki-Miyaura cross-coupling reaction compatible with cell growth and

131 However, under the optimized cross-coupling reaction conditions, the isomerization wa

132 Such stereospecific cross-coupling reactions constitute a powerful synthetic

133 This reductive cross-coupling reaction displays a fairly unusual anti s

134 spectroscopic studies suggest that this C-S cross-coupling reaction does not involve a Ni(0)-species

135 in monomers that participate in coupling and cross-coupling reactions during lignification in Norway

136 hentic monomer participating in coupling and cross-coupling reactions during lignification.

137 This method represents the first catalytic cross-coupling reaction employing a nonallylic and nonbe

138 ide N-C(O) bonds are generally unreactive in cross-coupling reactions employing low-valent transition

139 Cross-coupling reactions enable rapid, convergent synthe

140 This cross-coupling reaction enables the regioselective synth

141 terocycles participate in the Suzuki-Miyaura cross-coupling reaction, enabling entry into diverse bis

142 w compounds are also scaffolds for selective cross-coupling reactions, enabling further molecular div

143 ity of these intermediates is exemplified by cross-coupling reactions, enabling regiocontrolled synth

144 Starting with a Sonogashira cross-coupling reaction, enynol (10) was prepared.

145 an important role in a range of Ni-catalyzed cross-coupling reactions, especially those involving alk

146 ve been shown to undergo selective amide N-C cross-coupling reactions, feature a significantly decrea

147 chnology, high yield and reproducible Suzuki cross-coupling reaction for one of our key intermediates

148 ound to be the resting state in Pd-catalyzed cross-coupling reactions for a range of aryl halides and

149 Cross-coupling reactions for carbon-carbon and carbon-he

150 The utility of the Pd catalyst for the cross-coupling reactions for synthesizing branched conju

151 method complementary to the Stille or Suzuki cross-coupling reactions for the synthesis of cyclic or

152 e efficient synthetic tool, Buchwald-Hartwig cross-coupling reaction, for the functionalization of 1,

153 s have been synthesized by a modified Suzuki cross-coupling reaction from 3,4-dibromo-N-benzylmaleimi

154 ts into an iridium/nickel photocatalytic C-O cross-coupling reaction from time-resolved spectroscopic

155 t is noted that the one-pot pinacol boronate cross-coupling reaction generally provides products in h

156 We note that the tandem diboration/cross-coupling reaction generally provides products in h

157 Bronsted acid catalyzed dearomatizing redox cross coupling reaction has been realized, in which aryl

158 s in a challenging asymmetric Suzuki-Miyaura cross-coupling reaction has enabled enantioenriched (up

159 ant first-row metals, especially nickel, for cross-coupling reactions has attracted significant inter

160 he development of transition metal-catalysed cross-coupling reactions has greatly influenced the mann

161 and phenol derivatives as electrophiles for cross-coupling reactions has numerous advantages over co

162 e equivalents for transition metal-catalyzed cross-coupling reactions has the potential to substantia

163 proposed in numerous Ni-catalyzed reductive cross-coupling reactions-has been subject to speculation

164 rtant factors affecting the Buchwald-Hartwig cross-coupling reaction have been optimized.

165 Asymmetric Ni-catalyzed cross-coupling reactions have become a very attractive t

166 Transition-metal-catalysed cross-coupling reactions have become one of the most use

167 Csp(2)-Csp(3) cross-coupling reactions have been developed, but enanti

168 Examples of stereospecific, Pd-catalysed cross-coupling reactions have been reported for isolable

169 Transition-metal-catalysed cross-coupling reactions have been widely used for their

170 Advances in Pd-catalysed cross-coupling reactions have facilitated the developmen

171 Ni-catalyzed cross-coupling reactions have found important applicatio

172 Palladium-catalyzed cross-coupling reactions have transformed the exploratio

173 sters was obtained via a palladium-catalyzed cross-coupling reaction (Hirao coupling) of dialkyl phos

174 This elementary reaction enables a powerful cross-coupling reaction in which a chiral Pd catalyst me

175 catalysts opens new avenues in the design of cross-coupling reactions in organic synthesis.

176 Advances in metal-catalyzed cross-coupling reactions in the early 2000s brought a hi

177 e, purine, azaindole) can be utilized in the cross-coupling reaction, including those substituted wit

178 amental characterization of the key steps in cross-coupling reactions, including C-C bond-forming red

179 stration of three mild Pd/Cu-mediated Stille cross-coupling reactions, including the use of a one-pot

180 he useful two-step directed ortho metalation/cross-coupling reaction involving cryogenic temperature

181 Distinct from nickel-catalyzed cross-coupling reactions involving carbon-centered radic

182 ribe the use of MOFs as catalysts to promote cross-coupling reactions involving organometallic reacti

183 The Suzuki-Miyaura cross-coupling reaction is a foundation stone of modern

184 The SET-induced biaryl cross-coupling reaction is established as the first exam

185 media for thermomorphic palladium-catalyzed cross-coupling reactions is demonstrated.

186 effect of unprotected azoles on Pd-catalyzed cross-coupling reactions is described based on evidence

187 of gold as the organizing metal in homo- and cross-coupling reactions is explored in this paper combi

188 ubstrate class for nickel-catalyzed C(sp(3)) cross-coupling reactions is reported.

189 ugh an efficient palladium-catalyzed Ullmann cross-coupling reaction, is reductively cyclized under c

190 commercially available starting materials by cross-coupling reactions, many desirable and otherwise d

191 In the past 50 years, cross-coupling reactions mediated by transition metals h

192 yl: A significant development in alkyl-alkyl cross-coupling reactions, namely the nickel-catalyzed de

193 alyst under commonly employed conditions for cross-coupling reactions, noninhibitory byproduct releas

194 The Pd-catalyzed cross-coupling reaction of 1-acetyl-2-methyl-3H-pyrrolo[

195 oCl(2)/IAd.HBF(4) enables the Suzuki-Miyaura cross-coupling reaction of a broad range of aryl triflat

196 a quaternary center occurred through a rare cross-coupling reaction of a tertiary organometallic com

197 An efficient palladium-free Stille cross-coupling reaction of allylic bromides and function

198 xidative addition is the key step during the cross-coupling reaction of aryl halides has led to the d

199 atalyzed synthesis of diaryl selenides via a cross-coupling reaction of diaryl diselenides with aryl

200 Here, we report an iron-catalyzed cross-coupling reaction of electron-deficient heterocycl

201 The efficient Suzuki-Miyaura cross-coupling reaction of halogenated aminopyrazoles an

202 approach is based on the palladium-catalyzed cross-coupling reaction of halogenated azines with organ

203 Almost two decades passed before the first cross-coupling reaction of heteroatom-based electrophile

204 wn that the efficiency of the Suzuki-Miyaura cross-coupling reaction of nitroimidazoles is slightly l

205 An efficient Suzuki-Miyaura cross-coupling reaction of perfluorinated arenes with ar

206 is of (+)-ileabethoxazole (1) using a Stille cross-coupling reaction of propargylic stannanes with 5-

207 irst Negishi nickel-catalyzed stereospecific cross-coupling reaction of secondary benzylic esters is

208 al and highly stereoselective iron-catalyzed cross-coupling reaction of stereodefined enol carbamates

209 were prepared via the Liebeskind-Srogl (L-S) cross-coupling reaction of the Biellmann BODIPYs (1a,b)

210 the sp(2) C-H bond in water also allows the cross-coupling reaction of two different C-H bonds in th

211 l for the palladium-catalyzed Suzuki-Miyaura cross-coupling reaction of unprotected haloimidazoles is

212 This method relies on a palladium-catalyzed cross-coupling reaction of various brominated PAHs with

213 Palladium-catalyzed cross-coupling reactions of 2-bromobenzaldehyde and 6-br

214 Metal-catalyzed enantioconvergent cross-coupling reactions of alkyl electrophiles are emer

215 of our ongoing effort to expand the scope of cross-coupling reactions of alkyl electrophiles, we have

216 eavage of inert C(sp(2))-O bonds relevant to cross-coupling reactions of aromatic ethers catalyzed by

217 Cross-coupling reactions of aryl groups with alpha-fluor

218 that are typically used in Pd-catalyzed C-N cross-coupling reactions of aryl halides.

219 We report diverse C-N cross-coupling reactions of aryl thianthrenium salts tha

220 t adducts containing Si-O-Pd linkages in the cross-coupling reactions of arylsilanolates has been una

221 synthesis involved site-selective palladium cross-coupling reactions of chloropyrimidines with trior

222 Pd-catalyzed Suzuki-Miyaura and Sonogashira cross-coupling reactions of cyclic 1,3-diones in the syn

223 phosphorylation of nucleosides or by aqueous cross-coupling reactions of halogenated dNTPs is discuss

224 Suzuki-Miyaura cross-coupling reactions of heteroaromatics catalyzed by

225 d Suzuki, Negishi, Sonogashira, and Heck C-C cross-coupling reactions of iodo derivatives 1c, 1d, and

226 t adducts containing Si-O-Pd linkages in the cross-coupling reactions of organosilanolates has been u

227 Described herein are the cross-coupling reactions of sulfoxonium ylides with C(sp

228 Although metal-catalyzed cross-coupling reactions of unactivated alkyl electrophi

229 on condition screening for a radical-radical cross-coupling reaction on micro-fabricated interdigitat

230 ared by means of either the Liebeskind-Srogl cross-coupling reaction or the Vilsmeier reaction.

231 enamides that are useful building blocks for cross-coupling reactions or heterocyclic chemistry.

232 tions can be used directly in Suzuki-Miyaura cross-coupling reactions or isolated as air-stable potas

233 Within the realm of cross-coupling reactions, organotrifluoroborates provide

234 eterogeneous catalyst for the Suzuki-Miyaura cross-coupling reaction, outperforming its amorphous cou

235 Transition-metal-catalysed cross-coupling reactions, particularly those mediated by

236 Subsequent cross-coupling reactions proceed in excellent yields and

237 fluorinated amide, this palladium-catalyzed cross-coupling reaction provides a versatile platform to

238 ing of each module using palladium-catalyzed cross-coupling reactions provides both mono- and disubst

239 eboronative mechanisms with implications for cross-coupling reactions, regioselective deuteration/tri

240 secondary and tertiary alkyl nucleophiles in cross-coupling reactions remains a challenge because of

241 ication of C(sp3)-hybridized nucleophiles in cross-coupling reactions remains an unsolved challenge i

242 Employment of sulfoxides as electrophiles in cross-coupling reactions remains underexplored.

243 combining amination and palladium-catalyzed cross-coupling reactions, such as reductive dehalogenati

244 Reactions covered include common cross-coupling reactions, such as Suzuki, Heck, Kumada,

245 TTF building block using palladium-catalyzed cross-coupling reactions, such as the Suzuki reaction.

246 Moreover, 4,4'-bipyridine 2 was submitted to cross-coupling reactions (Suzuki and Sonogashira) which

247 In all cases, the cross-coupling reactions take place rapidly in DMSO in g

248 Pd-catalyzed cross-coupling reactions that form C-N bonds have become

249 In the area of transition metal-catalyzed cross-coupling reactions the C-S bond cleaving reactions

250 ces in transition-metal-catalyzed C(sp(3))-C cross-coupling reactions, there remain challenging bond

251 se apart from their effectiveness in Negishi cross-coupling reactions, they show more resistance to a

252 in photoredox Ni-catalyzed carbon-heteroatom cross-coupling reactions through a strategy that allows

253 uctions to build the polyol domain, a Stille cross-coupling reaction to assemble the polyene, and an

254 re used in a stereospecific nickel-catalyzed cross-coupling reaction to form C(sp(3))-C(sp(3)) bonds.

255 ynthesis features the stereoselective Stille cross-coupling reaction to set up the whole carbon frame

256 an also be accessed by harnessing the Suzuki cross-coupling reaction to the isomerization/N-acylimini

257 equent high yielding stereoretentive Negishi cross-coupling reactions to allow structural diversity t

258 An additional protocol that allows Suzuki cross-coupling reactions to be performed on bromo-substi

259 the most reactive precursors for N-C(O) bond cross-coupling reactions to date, wherein the reactivity

260 for subsequent oxidation, halogenation, and cross-coupling reactions to deliver benzylamine and aryl

261 ively proposed as a key step in Ni-catalyzed cross-coupling reactions to generate radical intermediat

262 ks late-stage diversification through Suzuki cross-coupling reactions to give mono-, di-, and trisubs

263 quinoline-based ligand is essential for the cross-coupling reactions to proceed.

264 ant (Hantzsch ester), whereas most reductive cross-coupling reactions use stoichiometric metals.

265 adium-catalyzed, enantioselective, aryl-aryl cross-coupling reaction using 1-naphthyldimethylsilanola

266 Iron-catalyzed cross-coupling reactions using alkynyl nucleophiles repr

267 s well as chemodivergent palladium catalyzed cross-coupling reactions using boronic acids are applied

268 In most cases, cross-coupling reactions using OACs proceed under milder

269 n the absence of Pd-catalyzed or Ni-mediated cross-coupling reactions, using 1,4-diketones as surroga

270 been synthesized by exploiting Pd-catalyzed cross-coupling reaction via C-H activation as a key step

271 The ability to perform the cross-coupling reaction was facilitated by the regio-con

272 The versatility of the glycosyl cross-coupling reaction was probed in the total synthesi

273 Their reactivity in a Negishi cross-coupling reaction was tested.

274 ruglike electrophiles (informers) in Negishi cross-coupling reactions was evaluated by high-throughpu

275 In a modular approach, using cross-coupling reactions, we synthesized a series of can

276 Using Suzuki-Miyaura cross-coupling reactions, we synthesized well-defined mo

277 oronic acid (p-tolyl-B(OH)2) in this type of cross-coupling reaction were evaluated (eg, ethyleneglyc

278 Suzuki and Sonogashira cross-coupling reactions were used to prepare the aryl a

279 Here, we present the first Suzuki cross-coupling reaction which utilizes dihalo compounds

280 ther been incorporated into a dual catalytic cross-coupling reaction, which requires both the supramo

281 e have on the dual-catalyzed decarboxylative cross-coupling reactions will be discussed.

282 ting oxidative additions upon d(0) metals or cross coupling reactions with cobalt(iii) without metal

283 fied by a palladium-catalyzed Suzuki-Miyaura cross-coupling reaction with (het)arylboronic acids.

284 anomeric stannanes undergo a stereospecific cross-coupling reaction with aromatic halides in the pre

285 through a palladium-catalyzed Suzuki-Miyaura cross-coupling reaction with arylboronic acids in good y

286 Pd(0)-catalyzed carbopalladation followed by cross-coupling reaction with boronic acids.

287 The compatibility of the Negishi cross-coupling reaction with the versatile B-Cl function

288 lic coupling partners in palladium-catalyzed cross-coupling reactions with (hetero)aryl halides.

289 roved to be more effective in catalyzing C-N cross-coupling reactions with a diverse selection of ami

290 these copper-rich complexes on the yields of cross-coupling reactions with an alkyl halide was tested

291 be used as nucleophilic components in Stille cross-coupling reactions with aryl bromides.

292 ter for onward reactivity as demonstrated in cross-coupling reactions with benzoyl chloride that prod

293 arries mechanistically distinct, traditional cross-coupling reactions with C-H functionalization usin

294 ed the development of elusive amide bond N-C cross-coupling reactions with organometallic reagents, a

295 is demonstrated to be effective in selective cross-coupling reactions with secondary alkyl reagents a

296 les broad compatibility of carbon-heteroatom cross-coupling reactions with sensitive substrates and f

297 While iron-catalyzed Kumada cross-coupling reactions with simple iron salts have bee

298 ondary alkyltrifluoroborate reagents undergo cross-coupling reactions with stereospecific inversion o

299 ant implications for the design of new amide cross-coupling reactions with the N-C(O) amide bond clea

300 phine ligands for efficient room temperature cross-coupling reactions with unactivated aryl chlorides