ライフサイエンスコーパス: cross-coupling reaction

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

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

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

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

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

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

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

8 the two positions toward the metal-catalyzed cross-coupling reaction.

9 a common intermediate using a silicon-based cross-coupling reaction.

10 amolecular enolate-driven palladium-mediated cross-coupling reaction.

11 as well as an alkenyl-alkenyl silicon-based cross-coupling reaction.

12 ti-substituted 3-fluorofurans using a Suzuki cross-coupling reaction.

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

14 unctionality was accomplished by Sonogashira cross-coupling reaction.

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

16 se cycloaddition reactions have been used in cross coupling reactions.

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

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

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

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

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

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

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

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

25 ally prepared through kinetically controlled cross-coupling reactions.

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

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

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

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

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

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

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

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

34 nsights into the mechanism of gold-catalyzed cross-coupling reactions.

35 re synthesized by double palladium-catalyzed cross-coupling reactions.

36 or exploited using versatile metal-catalysed cross-coupling reactions.

37 ion under the conditions of copper-catalyzed cross-coupling reactions.

38 kage and using multifold palladium-catalyzed cross-coupling reactions.

39 ification through S(N)Ar and metal-catalyzed cross-coupling reactions.

40 of chiral 4,4'-bipyridines by site-selective cross-coupling reactions.

41 on were further diversified via Pd-catalyzed cross-coupling reactions.

42 ersal partners (2 and 6) for metal-catalyzed cross-coupling reactions.

43 Diels-Alder cycloadducts were used in Hiyama cross-coupling reactions.

44 s such as arylboronic acids in Au(I)/Au(III) cross-coupling reactions.

45 ficiently be used as a precursor for Negishi cross-coupling reactions.

46 vinyl chlorides and subsequent Pd-catalyzed cross-coupling reactions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

64 rivative was synthesized via the Sonogashira cross-coupling reaction and radiolabeled via the tricarb

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

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

67 ecent findings in transition metal-catalysed cross-coupling reactions and detail several reports from

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

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

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

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

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

73 e, Suzuki, Buchwald-Hartwig, and Sonogashira cross-coupling reactions) and lithium-halogen exchange t

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

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

76 ely synthesized, using a palladium-catalyzed cross-coupling reaction, and identified as potent antipr

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

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

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

80 th the activity and regioselectivity of this cross-coupling reaction are correlated with the acidity

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

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

83 Cross-coupling reactions are among the most widely utili

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

85 Room-temperature Suzuki-Miyaura cross-coupling reactions are mediated by Pd(CNAr(Dipp2))

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

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

88 In cross-coupling reactions, azobenzenes therefore usually

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

90 ted a typically undesired elementary step in cross-coupling reactions, beta-hydride elimination, to a

91 diene was installed with a complex reductive cross-coupling reaction between a preformed Ti-alkyne co

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

93 ated the two-step, one-pot borylation/Suzuki cross-coupling reaction between aryl and heteroaryl hali

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

95 A nickel-catalyzed cross-coupling reaction between N-sulfonyl aziridines an

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

97 Weinreb amides through a palladium-catalyzed cross-coupling reaction between organoboronic acids and

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

99 Complex 3a was found to catalyze the Kumada cross-coupling reaction between PhMgCl and a range of br

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

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

102 Here, we describe a metal-promoted reductive cross-coupling reaction between vinylcyclopropanes and a

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

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

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

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

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

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

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

110 ed that an enolate-driven palladium-mediated cross-coupling reaction can be accomplished by a copper-

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

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

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

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

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

116 n and the sulfanyl group by Liebeskind-Srogl cross-coupling reaction, demonstrating the orthogonality

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

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

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

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

121 The cross-coupling reactions enable these silicon dienes to

122 This cross-coupling reaction enables the regioselective synth

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

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

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

126 Palladium-catalyzed cross-coupling reactions, especially those involving Zn,

127 The explication of how this new class of cross-coupling reactions evolved from problem formulatio

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

129 eature the development of the B-alkyl Suzuki cross-coupling reaction for direct access to (E)-cyclono

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

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

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

133 C,C cross-coupling reactions for the synthesis of nonsymmetr

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

135 lizing sequential, orthogonal Suzuki-Miyaura cross-coupling reactions from two late-stage intermediat

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

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

138 A subsequent cross-coupling reaction gives access to highly substitut

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

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

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

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

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

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

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

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

147 tility of these compounds is demonstrated in cross-coupling reactions, highlighting the potential of

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

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

150 nts 2a and 2b were prepared and subjected to cross-coupling reactions in the presence of a nickel cat

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

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

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

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

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

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

157 A Pd-catalyzed cross-coupling reaction is also described and easily yie

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

159 A novel catalytic alkyne cross-coupling reaction is reported which connects terti

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

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

162 roviding the full catalytic cycles for these cross-coupling reactions is described.

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

164 ysts as a convenient source of LPd(0) in C-N cross-coupling reactions is explored.

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

166 hos) that shows excellent reactivity for C-N cross-coupling reactions is reported.

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

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

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

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

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

172 One-pot tandem Diels-Alder/cross coupling reactions of 2-boron substituted dienes a

173 Formation on demand: An organocatalytic cross-coupling reaction of aldehydes with N-hydroxyimide

174 We report here the iron-catalyzed cross-coupling reaction of alkyl vinyl halides with thio

175 versal of regioselectivity in a Pd-catalyzed cross-coupling reaction of an aryl chloro triflate with

176 The cross-coupling reaction of aryl bromides and iodides wit

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

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

179 During work on a copper-catalyzed cross-coupling reaction of ethyl (E)- and (Z)-3-iodoacry

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

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

182 Palladium catalyzed cross-coupling reaction of hydrazones with aryl halides

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

184 sis was performed for the k(c) values of the cross-coupling reaction of nitroxides with tert-butoxylc

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

186 conditions were found for the Suzuki-Miyaura cross-coupling reaction of potassium cyclopropyl- and cy

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

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

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

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

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

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

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

194 , are shown to serve as suitable partners in cross-coupling reactions of (activated) secondary alkyl

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

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

197 xanediol ligand facilitated the Cu-catalyzed cross-coupling reactions of alkyl, aryl, or heterocyclic

198 The cross-coupling reactions of allylboronic acid pinacol es

199 Copper-catalyzed cross-coupling reactions of amidine salts were utilized

200 stereochemical course of palladium-catalyzed cross-coupling reactions of an enantioenriched, alpha-su

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

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

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

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

205 leoside triphosphates (dNTPs) by the aqueous cross-coupling reactions of biarylboronates is reported.

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

207 or 168 different Pd/Cu-catalyzed Sonogashira cross-coupling reactions of five arylacetylenes (phenyla

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

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

210 Selectivity of the palladium-catalyzed cross-coupling reactions of heterocycles bearing multipl

211 tematic study of titanium-mediated reductive cross-coupling reactions of internal alkynes with termin

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

213 ickel-based catalysts have been reported for cross-coupling reactions of nonactivated alkyl halides.

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

215 The mechanism of palladium-catalyzed cross-coupling reactions of potassium (4-methoxyphenyl)d

216 oduct total synthesis of palladium-catalyzed cross-coupling reactions of silicon derivatives.

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

218 e pyri(mi)dyl bromides and then Pd-catalyzed cross-coupling reactions of the amines and precursor bro

219 The Suzuki-Miyaura cross-coupling reactions of the borylated polysulfones w

220 The first Suzuki-Miyaura cross-coupling reactions of the synthetically versatile

221 subsequent TBAF-assisted/Pd-catalyzed Hiyama cross-coupling reactions of those Diels-Alder adducts.

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

223 In the cross-coupling reactions of unprotected oxindoles with a

224 l step was also possible by Liebeskind-Srogl cross-coupling reaction on the previously introduced C-2

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

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

227 iciently displaced by S(N)Ar, Suzuki-Miyaura cross-coupling reaction, or reduction.

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

229 eding through a Pd(II)-catalyzed Diels-Alder/cross coupling reaction pathway.

230 Subsequent cross-coupling reactions proceed in excellent yields and

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

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

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

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

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

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

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

238 different chemoselectivity than conventional cross-coupling reactions, such as the Suzuki-Miyaura, St

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

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

241 A catalytic intermolecular cross-coupling reaction that couples secondary alpha-bro

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

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

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

245 f styrene, followed by a palladium-catalyzed cross coupling reaction to install an electron donating

246 A mild cross-coupling reaction to access several N-alkenyl-subs

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

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

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

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

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

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

253 triflate products can be elaborated through cross-coupling reactions to generate synthetically usefu

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

255 This cross-coupling reaction tolerates various functional gro

256 Cross-coupling reactions typically rely on the use of tr

257 lete conversions of aryl chlorides in Suzuki cross-coupling reactions under Pd(I) dimer conditions.

258 The late-stage alkenyl-alkenyl silicon-based cross-coupling reaction uniting the core alkenyl iodides

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

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

261 thway is important in further development of cross-coupling reactions using different catalysts.

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

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

264 The critical copper-mediated cross-coupling reaction was expanded to include guanidin

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

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

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

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

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

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

271 The cross-coupling reactions were found to proceed best with

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

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

274 The strategic step is a Suzuki-Miyaura cross-coupling reaction, which has allowed the preparati

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

276 We anticipate that this Pd-catalyzed cross-coupling reaction will open new avenues for synthe

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

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

279 siloxane ring, followed by an intramolecular cross-coupling reaction with a pendant alkenyl iodide.

280 Palladium-catalyzed Suzuki-Miyaura (SM) cross-coupling reaction with allylboronic acid pinacol e

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

282 l anion equivalents in a palladium-catalyzed cross-coupling reaction with aryl bromides to give unsym

283 es undergo a stereospecific nickel-catalyzed cross-coupling reaction with aryl Grignard reagents (see

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

285 een prepared through a series of Sonogashira cross-coupling reactions with 62% overall yield.

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

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

288 rate both the importance of Fe(I) in Negishi cross-coupling reactions with arylzinc reagents and the

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

290 unds served as starting materials for Suzuki cross-coupling reactions with electron-poor arylboronic

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

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

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

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

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

296 boronate in nickel-catalyzed Suzuki-Miyaura cross-coupling reactions with the two C-O electrophiles,

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

298 (N-methylheteroaryl)borates and their use in cross-coupling reactions with various aryl and heteroary

299 philic addition followed by Liebeskind-Srogl cross-coupling reaction yielded unprecedented aryl intro

300 This reductive cross-coupling reaction yields anti-Markovnikov products