ライフサイエンスコーパス: olefin

1 + 2] photocycloaddition of the enone to the olefin.

2 strategies toward the stereochemistry of the olefin.

3 y of the enolate or the accompanying allylic olefin.

4 with excellent stereocontrol of the internal olefin.

5 alue products from simple feedstocks such as olefins.

6 xidative dehydrogenation (ODH) of alkanes to olefins.

7 in the hydrophosphanation of a wide range of olefins.

8 reochemical outcomes in the hydrogenation of olefins.

9 d by its high shape selectivity toward light olefins.

10 nertness of the typical unactivated internal olefins.

11 t the arylation of tri- and tetrasubstituted olefins.

12 copolymerization of polar vinyl monomers and olefins.

13 ew carbon-carbon bonds and two stereodefined olefins.

14 ge the gap" between polar vinyl monomers and olefins.

15 ve manner with electron-deficient dienes and olefins.

16 ant metal provides a sustainable strategy to olefins.

17 bstituted alkenes to form new trisubstituted olefins.

18 give the corresponding 1,2-difunctionalized olefins.

19 betulin with HCl or K10 produced abeo-lupane olefins.

20 despite its deactivation toward hydrocarbon olefins.

21 ng blocks on route to all-carbon substituted olefins.

22 the Rh-catalyzed asymmetric hydrogenation of olefins.

23 tion of new carbonyl reactivity to construct olefins.

24 these reactive intermediates with activated olefins, 1,3-dipoles, and dienes, the process generates

25 Fe-mediated HAT reaction of the intermediate olefin 2, effecting a transannular C20-C2 free radical c

26 hydrogenation sensitive examples such as an olefin, a ketone, nitriles, nitro groups, and an aryl io

27 tion of this alkyl radical with the revealed olefin acceptor in turn produces a ring-expanded ketone

28 f C(sp(3))-H bond of 8-methylquinolines with olefins (acrylates, styrenes, and aliphatic) is reported

29 scope with respect to quinoline N-oxides and olefins (activated acrylates and styrenes; unactivated a

30 vity relationships reflect the preference of olefin activation over free amine coordination, which is

31 a Cu(I) precatalyst that achieves selective olefin activation via coordination to the metal center.

32 e recent advances in selective reductions of olefins, alkynes, carbonyl and carboxylic derivatives, i

33 nes are established substrates for ARC-based olefin amination under similar conditions.

34 ules in a cross-coupling fashion we describe olefin amine (OLA) reagents for the transformation of al

35 A new class of intermolecular olefin aminooxygenation reaction is described.

36 vicinal 1,2-diamines using readily available olefin and amine building blocks.

37 .1]-bridged bicycles along with an exocyclic olefin and an all-carbon quaternary stereocenter.

38 retained the cis-stereoconfiguration of the olefin and yielded a hard semicrystalline polymer (T(m)

39 s were generally more reactive than terminal olefins and afforded appreciable quantity of cycloadduct

40 in homogeneous catalyzed hydrometalation of olefins and alkynes.

41 The direct coupling of olefins and amines would be an ideal approach to constru

42 A diverse array of olefins and amines, including hetreroarylamines that do

43 The often-utilized olefins and benzoates, as well as benzylidene-, silyl-,

44 ve multicomponent reactions (MCRs) involving olefins and C-N electrophiles are a powerful tool to rap

45 chnology that directly converts methane into olefins and higher hydrocarbons.

46 previously unreactive disubstituted terminal olefins and internal olefins, are compatible with this t

47 site site-selectivity pattern for both alpha-olefins and internal olefins, thus unlocking a new catal

48 and diastereoselective hydrogenation of such olefins and the mechanistic insights of the reaction.

49 s compatible with both internal and terminal olefins and tolerates a diverse array of functional grou

50 thesis involves halogenation of linear alpha-olefins and would be expected to produce linear alkanes.

51 ed from an aldehyde and an acyl bromide), an olefin, and a hydrosilane, catalyzed by nickel, an earth

52 f heteroaromatic carboxylic acids as well as olefins, and facilitates a diverse array of high-value o

53 ct, masking-reagent-free propylene and amino-olefin (AO, CH(2) =CH(CH(2) )(x) N(n) Pr(2) , x=2, 3, 6)

54 akes over long before significant amounts of olefins are formed, thus guiding the interpretation of e

55 A range of acyclic and cyclic cis-olefins are suitable substrates, and the reaction is ope

56 disubstituted terminal olefins and internal olefins, are compatible with this transformation.

57 hetically inert unactivated acyclic internal olefins as allylic surrogates.

58 of controlling molecular weight, using alpha olefins as chain transfer agents.

59 actor model that includes autocatalysis with olefins as cocatalysts is one able to understand the ini

60 saturated azacycles using readily available olefins as coupling partners.

61 ability to use readily accessible and stable olefins as surrogates for organometallic nucleophiles.

62 enzyme, a non-heme iron enzyme, can catalyze olefin aziridination and nitrene C-H insertion, and that

63 Olefin aziridination via organocatalytic nitrene transfe

64 Diaryl, aryl-alkyl, and alkyl-alkyl olefins bearing a variety of substituents are all diamin

65 , which shows poor activity towards terminal olefins because of the formation of a stable off-cycle m

66 en undergoes oligomerization into six-carbon olefins before polymerizing into indistinguishable carbo

67 ion kinetics were due to the cis-macrocyclic olefin being less flexible and having a larger populatio

68 ate involved in the catalytic epoxidation of olefins by [(cyclam)Fe(II) ](2+) and H(2) O(2) .

69 erization of 1-alkene monomers into internal olefins by adding a Lewis acid.

70 kovnikov hydroarylation of 1,1-disubstituted olefins by dual palladium and copper hydride catalysis a

71 Generated olefins can be further transformed in a highly stereosel

72 ive synthesis of all-carbon tetrasubstituted olefins can be realized via alkenyl halide- or triflate-

73 d-diimine catalyzed polymerizations of alpha-olefins can drastically alter reactivity.

74 oenzymatic intermolecular hydroalkylation of olefins catalyzed by flavin-dependent 'ene'-reductases.

75 Formation of the unsubstituted olefin (-CH=CH-) linkage upon reticulation is confirmed

76 weight can be tuned by varying the ratio of olefin/chain-transfer agent.

77 tude of further derivatizations ranging from olefin chemistry to C-H activation, giving rise to a div

78 Remarkably, introducing the amino-olefin comonomers significantly enhances stereoselection

79 roup-free approach relies on a chiral Ir-(P, olefin) complex and Mg(ClO(4) )(2) Lewis acid catalyst s

80 unsymmetrically all-carbon tetrasubstituted olefin containing oxindoles from readily accessible anil

81 rted, have been achieved for a wide range of olefins containing relevant poorly coordinative groups s

82 A cyclic olefin copolymer (TOPAS) suspended-core fiber guiding in

83 dic micropillar arrays, produced from cyclic olefin copolymer using high-fidelity microfabrication, a

84 Olefin copolymers are complex polymer materials that exh

85 As representative examples, blends of olefin copolymers have been fractionated on porous graph

86 rough sequential Fe(III)-catalyzed reductive olefin coupling and Dieckmann condensation.

87 lic alcohols are shown to be highly reactive olefin coupling partners leading to a directed diastereo

88 A variety of olefin coupling partners, including previously unreactiv

89 xidative condensation, intramolecular anodic olefin coupling reactions, an amide oxidation, and a med

90 alcohols for ruthenium benzylidene catalyzed olefin cross-metathesis with homoprenyl benzenes.

91 d a representative part of the autocatalytic olefin cycle (63 steps).

92 pment of catalytic Sm(II) 5- exo- trig ketyl olefin cyclization reactions.

93 amolecular Diels-Alder reaction and an enone-olefin cycloaddition/fragmentation sequence are then emp

94 crylates and styrenes; unactivated aliphatic olefins) demonstrates the robustness of the developed ca

95 ns active toward metathesis of electron-rich olefins, despite its deactivation toward hydrocarbon ole

96 abolism was extensive, with 5-OH-IMI and IMI-olefin detected at greater concentrations than IMI in ti

97 Olefins devoid of directing or activating groups have be

98 o be installed in a singular, chemoselective olefin difunctionalization.

99 of the art and outlook in synthesis of light olefins, dimethyl ether, liquid fuels, and alcohols thro

100 ve carboxylate derivatives and electron-poor olefins, displaying surprising water and air-tolerance a

101 and bromohydrin disulfonate, originated from olefin disulfonate species, present as side-products of

102 tional (DFT) studies reveal that the pendent olefin does not only act as an indispensable element for

103 ted the development of an electron-deficient olefin (EDO) ligand, Fro-DO, that promotes the generatio

104 ocatalytic dicarbofunctionalization (DCF) of olefins enabled by the merger of Giese-type addition wit

105 Current routes of olefin epoxidation either involve hazardous reagents or

106 t in oxygen atom transfer reactions, such as olefin epoxidation, in the presence of a small amount of

107 udies provide insights into the mechanism of olefin epoxidation, including an approximate first-order

108 s supported on silicates is investigated for olefin epoxidation.

109 ary products (asphalt, lubricant, wax, light olefins, etc.).

110 The conversion reaction also produces light olefins ethylene, propylene, and butenes, totalling a yi

111 olymer syntheses have been demonstrated with olefins (ethylene and 1-hexene) which produce amorphous

112 which pai-participation by the nucleophilic olefin facilitates chloride ionization and thereby circu

113 9 is introduced by azidation of the C-9/C-10 olefin, followed by reduction and lactam formation betwe

114 le playing a critical role in activating the olefin for concomitant electrophilic attack.

115 adicals for coupling with electron-deficient olefins for the generation of unnatural gamma-quaternary

116 by two key steps, including polysubstituted olefin formation and cyclization.

117 e reaction sequence that ultimately leads to olefin formation and strikingly demonstrates that only w

118 to Wittig chemistry are needed to construct olefins from carbonyl compounds, but none have been deve

119 and characterization of new P=C analogues of olefins from readily available starting materials is rep

120 nkers facilitated synthesis and provided the olefin functionality needed for ED-ROMP.

121 FBs exhibit remarkable stability to standard olefin functionalization reactions in spite of the penda

122 approach is notable, as only two additional olefin functionalizations are needed to construct the fu

123 It is the simplest olefin gas and is biosynthesized by plants to regulate p

124 c in the regard that the E-Z-geometry of the olefin governs the stereochemistry of the hydrogenation,

125 e rearrangement of disubstituted unactivated olefins has been achieved using a hypervalent iodine(III

126 esis between acrylamides and common terminal olefins has been developed by the use of novel cyclometa

127 cade reaction of aromatic diazo ketones with olefins has been developed.

128 (CDC) of heteroarenes with readily available olefins has been devised employing water as green solven

129 All-carbon tetrasubstituted olefins have been found in numerous biologically importa

130 ctive intermolecular transfer of carbenes to olefins, heterocycles, aldehydes, and amines.

131 Despite the presence of excess olefin, high selectivities are observed for secondary ov

132 ic resolution (DKR) of chiral 4-pentenals by olefin hydroacylation.

133 s of amides and thiols relevant to catalytic olefin hydroamidation reactions.

134 A photocatalytic olefin hydroaminoalkylation brings together three readil

135 fills a synthetic chemistry gap of existing olefin hydroazidation procedures, and thereby provides a

136 f a hydrogenation catalyst enables selective olefin hydrogenation, even in the presence of multiple s

137 Olefin hydrophosphanation is an attractive route for the

138 e Pt(1)@PDMS-PEG shows ultrahigh activity in olefin hydrosilylation with excellent terminal adducts s

139 If the olefin in the tether was trisubstituted (3'-methyl-2'-bu

140 lar factors influence the diffusion of light olefins in a complex environment with confined hydrocarb

141 ic acid across a wide variety of unactivated olefins in both complex molecules and unfunctionalized c

142 ety of electronically and sterically diverse olefins in excellent yield and high enantio- and diaster

143 ss-metathesis of pre-existing trisubstituted olefins in other relay-actuated Delta(6,7)-functionalize

144 xidative dehydrogenation (ODH) of alkanes to olefins in the gas phase.

145 ol, the macromonomers were prepared with cis-olefins in the metathesis-active segment.

146 anti-Markovnikov hydrocyanation of terminal olefins in which oxazoles function as nitrile equivalent

147 functional groups on both the arene and the olefin including fluoride, chloride, trifluoromethyl, es

148 midine-based directing group facilitates the olefin insertion by overcoming inertness of the typical

149 s and underlines that sigma-bond metathesis, olefin insertion, and olefin metathesis are in fact isol

150 pai-Character is also a requirement for olefin insertion, indicating its similarity to sigma-bon

151 c allene enantiomers through stereoselective olefin insertion, loss of the resultant stereochemical i

152 otes olefin isomerization through sequential olefin insertion/beta-hydride elimination.

153 istic constraints of carbonyl excitation and olefin interception have limited this attractive oxetane

154 volves forming a metal-stabilized anti-Bredt olefin intermediate.

155 the I(2)aa and I(9)aa ring systems by way of olefin intermediates that underwent Pd-catalyzed C-H bon

156 In converting a ketone with a pendant olefin into a cycloalkene and a simple carbonyl byproduc

157 ies on transfer hydrogenation of an acceptor olefin is developed with excellent E/Z selectivity and r

158 Moreover, a one-pot formal aminoacylation of olefins is described through a sequential cyclopropanati

159 alytic deaminative alkylation of unactivated olefins is described.

160 The asymmetric catalytic hydrogenation of olefins is one of the most widely studied and utilised t

161 , regioselective alkylation and arylation of olefins is possible.

162 catalysis for electrophilic thiocyanation of olefins is reported.

163 Modifying the electronic properties of olefins is the quintessential approach to tuning alkene

164 Off-cycle olefin isomerization catalyzed by the same Co(-I) active

165 with different configurations, suggesting an olefin isomerization reaction due to the decomposition o

166 on of an iron-hydride species which promotes olefin isomerization through sequential olefin insertion

167 rubbs second-generation catalyst followed by olefin isomerization using a catalytic amount of RuCl(2)

168 incorporate the most attractive features of olefin isomerization.

169 term this unique convergence of all possible olefin isomers global diastereoconvergence.

170 ent of new fluids has focused on fluorinated olefins, known as hydrofluoroolefins (HFOs), and blends

171 Ms (after NO release) derived from a triaryl olefin lead.

172 a stepwise addition occurs with the diene or olefin, leading to a zwitterionic intermediate that unde

173 either an alkyl Grignard reagent or terminal olefin ligand exchange coupling partner is described.

174 mple of such a reactive intermediate with an olefin ligated to the ruthenium center has been isolated

175 obustness is attributed to the unsubstituted olefin linkages.

176 The first unsubstituted olefin-linked covalent organic framework, termed COF-701

177 ent, with no dependence of binding energy on olefin loading up to one olefin per Cu(I).

178 with confined hydrocarbon pool species, high olefin loadings, and the presence of acid sites by means

179 Ring-closing olefin metathesis (RCM) then affords the closed-loop kno

180 tionic complex is crucial in order to become olefin metathesis active.

181 al was tested for gas phase and liquid phase olefin metathesis and exhibited higher catalytic activit

182 here add to the body of mechanistic work for olefin metathesis and may inform the continued design of

183 sible-light-controlled metathesis by merging olefin metathesis and photoredox catalysis.

184 sigma-bond metathesis, olefin insertion, and olefin metathesis are in fact isolobal reactions.

185 antioselective processes, C-H activation, or olefin metathesis are still rarely discussed.

186 ance of the heterogeneous tungsten-oxo-based olefin metathesis catalyst (WO(3)/SiO(2)) in industry, u

187 substrate concentration up to 25 mM using an olefin metathesis catalyst selectively immobilized insid

188 Access to leading olefin metathesis catalysts, including the Grubbs, Hovey

189 s of the active Fe(III) and Ga(III) carbonyl-olefin metathesis catalysts.

190 stable species, its concentration can impact olefin metathesis in other ways.

191 ally controlled catalytic Z- and E-selective olefin metathesis is introduced.

192 Olefin metathesis is now one of the most efficient ways

193 rrangement were synthesized via ring-closing olefin metathesis of bis(allyoxy)methyl derivatives usin

194 erstanding about the underlying mechanism in olefin metathesis of this new type of catalysts.

195 ination of a highly stereoselective tethered olefin metathesis reaction and a Julia-Kocienski olefina

196 es can be manipulated and managed so that an olefin metathesis reaction may occur more efficiently an

197 Catalytic carbonyl-olefin metathesis reactions have recently been developed

198 Ethylene is the byproduct of olefin metathesis reactions that involve one or more ter

199 aden the current scope of catalytic carbonyl-olefin metathesis reactions.

200 The olefin metathesis step can be carried out with substrate

201 @SiO(2-700) was shown to be highly active in olefin metathesis upon removal of pyridine ligands throu

202 alities so that MOPs can be cross-linked via olefin metathesis using Grubbs second generation catalys

203 cellent catalytic performances in asymmetric olefin metathesis with high enantioselectivities (up to

204 loping well-defined iron-based catalysts for olefin metathesis would be a breakthrough achievement in

205 or conjugation to other molecules (e.g., by olefin metathesis, peptide ligation, etc.).

206 bilization chemistries, such as ring-closing olefin metathesis, to stabilize loop, turn, and alpha-he

207 his work, we report a novel and short Grubbs olefin metathesis-mediated synthesis of methylene and di

208 and reduced W(IV) sites in the initiation of olefin metathesis.

209 Herein, we report a short olefin-metathesis-based total synthesis of Delta(12)-PGJ

210 m one substrate can be facilitated, isomeric olefin mixtures commonly found in petroleum-derived feed

211 -B(pin), the vinyl, or the 1,2-disubstituted olefin moieties were carried out to demonstrate versatil

212 ariety of functional groups on quinoline and olefin moieties.

213 idation via oxygen atom transfer (OAT) to an olefin moiety is mainly derived from the studies on thio

214 erstood facets of d(0) metal-catalyzed polar olefin monomer copolymerization processes.

215 A dual seven-membered cyclic carbonate/olefin monomer was synthesized from CO(2) and cis-1,4-bu

216 olefins that cannot be readily prepared from olefin monomers; however, controlled and living carbene

217 The initiation of the methanol-to-olefins (MTO) process is investigated using a multiscale

218 ism here proposed involves an N-heterocyclic olefin (NHO) catalytic species that acts as a nucleophil

219 of nitrous oxide (N(2)O) with N-heterocyclic olefins (NHOs) results in cleavage of the N-O bond and f

220 h an exocyclic double bond (= N-heterocyclic olefins, NHOs) has been determined using DFT calculation

221 lso induces a face-selective reaction of the olefin of the allylic group, leading to a highly diaster

222 ith, for instance, highly electron-deficient olefins, offers a compelling strategy to design chemical

223 l intermediates production, nickel-catalyzed olefin oligomerization is still a very dynamic topic, wi

224 Possible olefin or oxygen chelation from ring-opened CPE substitu

225 f propane and isobutane to the corresponding olefins over metal oxide catalysts.

226 corporated into MFU-4l preferentially adsorb olefins over paraffins.

227 3)O(8)Me](2-) (6) and with aldehydes to give olefins [P(3)O(8)CHCHR](2-) (7a: R = H; 7b: R = 4-C(6)H(

228 The potential of this material for olefin/paraffin separation under ambient conditions was

229 hrough experiments for an equimolar ratio of olefin/paraffin.

230 f binding energy on olefin loading up to one olefin per Cu(I).

231 ficantly, this intermolecular 2 + 2 carbonyl-olefin photocycloaddition engages alkyl ketones, which a

232 ategy to regulate branching in chain-walking olefin polymerization by triggering a rapid isomerizatio

233 explains the H(2) response observed in d(0) olefin polymerization catalysts and underlines that sigm

234 efforts aimed at developing new homogeneous olefin polymerization catalysts, with a primary focus on

235 new catalyst systems, especially for group 4 olefin polymerization catalysts.

236 of the target phenethylamines over competing olefin polymerization products.

237 s advances in group 4-centered catalysis for olefin polymerization, successful examples of ethylene +

238 achieved remarkable success in conventional olefin polymerizations, encounter severe limitations her

239 functional groups was also observed, such as olefins possessing esters, sulfone, amide, cyanide, and

240 The methanol-to-olefins process over H-SAPO-34 is characterized by its h

241 etal-organic frameworks differing in the E/Z olefin ratio were prepared either by the previous isomer

242 es for the production of polymer-grade lower olefins remains an important and challenging goal for ma

243 of unfunctionalized tetrasubstituted acyclic olefins remains the pinnacle of asymmetric synthesis and

244 The enantioselective hydrocyanation of olefins represents a conceptually straightforward approa

245 addition and 1,2-cycloaddition with dienes + olefins, respectively.

246 Iron(III)-catalyzed carbonyl-olefin ring-closing metathesis employs reactivity not ty

247 development of Lewis acid-catalyzed carbonyl-olefin ring-closing metathesis reactions for aliphatic k

248 zed cis- trans isomerization of the employed olefins seem not to be an important side reaction here.

249 unctionalized products (aldehydes, alcohols, olefins) show bistability when varying the hydrogen/carb

250 zation of propylene and other nonpolar alpha-olefins, stereoselective polymerization of polar vinyl m

251 ad natural products based on calculations of olefin strain energies, NMR chemical shifts and coupling

252 Group 4 catalyst-amino-olefin structure-activity-selectivity relationships refl

253 The synthesized monomer with two terminal olefin structures has great free radical polymerization

254 Synthesis of 1,1-deactivated olefins substituted with a BT-sulfonyl group and a carbo

255 reliably controlled via substituents on the olefin substrate, providing a means to convert a simple

256 ant discoveries that allow these challenging olefin substrates to be efficiently transformed.

257 te a sustainable and safe route to epoxidize olefin substrates using water as the oxygen atom source

258 Copolymerizations of ethylene with alpha-olefins such as 1-hexene and 1-octadecene, as well as te

259 lfonate species, present as side-products of olefin sulfonate production.

260 Disinfection of a commercial C(12)-olefin sulfonate surfactant mixture revealed dodecene su

261 We report the first identification of olefin sulfonate surfactant-derived DBPs from laboratory

262 nd aldehyde deformylating oxygenase (Ado) or olefin synthase (Ols).

263 nd facilitates a diverse array of high-value olefin-tethered heteroarenes in high yields (up to 87%).

264 compute the T(1)-S(0) free energy gap of the olefin-tethered precursors and also to predict their rea

265 e of a phosphite group extended the range of olefins than can be efficiently hydrogenated.

266 It is the substitution pattern of the olefin that determines whether metathesis or cyclopropan

267 ilable bifunctional silyl ether-based cyclic olefins that copolymerize efficiently with norbornene-ba

268 esis activity for both terminal and internal olefins that is consistent with the lower stability of M

269 For cis allylic olefins, the trend is reversed.

270 For trans allylic olefins, the Z- and E-enol ethers proceed through chair

271 tion of highly electrophilic 1,1-deactivated olefins, their use as novel synthetic building blocks, a

272 lar factors influence the diffusion of light olefins through the 8-ring windows of H-SAPO-34.

273 pattern for both alpha-olefins and internal olefins, thus unlocking a new catalytic platform to forg

274 lective functionalization of a wide array of olefins to furnish iodination products as single stereoi

275 elective alkylation of aldehydes with simple olefins to selectively yield linear coupling products.

276 e-step hydrosulfamoylation using inexpensive olefins, tris(trimethylsilyl)silane, and photocatalyst E

277 mentally, increasing Cu(I) loading increased olefin uptake without affecting the binding energy, as p

278 molybdenum-catalyzed epoxidation reaction of olefins using alkyl hydroperoxides, that the molybdenum-

279 alladium diimine-catalyzed polymerization of olefins using unsaturated alcohols as chain-transfer age

280 thyl oleate (i.e., transformation into alpha-olefins via cross-metathesis with C(2)H(4)), Ru-1 is com

281 s (cata-HBCs) were synthesized from tetraryl olefins via iodine- and iron chloride-catalyzed oxidativ

282 ses (vinyl monomers and ring-strained cyclic olefins) via living photopolymerization.

283 are added simultaneously across a variety of olefins (vinyl amides, vinyl boranes, vinyl phosphonates

284 Catalytic hydrogenation of olefins was also facilitated by the sulfated zirconia-su

285 Because olefins were formed in this transformation, it showed so

286 C(5)H(4)N] where R = (i)Pr or Me, L(2) = bis-olefin), were characterized by single-crystal X-ray diff

287 vnikov hydroazidation method for unactivated olefins, which is promoted by a catalytic amount of benc

288 f a hydroxy- or a carboxylic-acid-containing olefin with commercially available HB(pin) or readily ac

289 g the hydroaminomethylation of diverse alpha-olefins with a wide range of alkyl, aryl, and heteroaryl

290 In contrast, initiation of olefins with allylic C-H groups (e.g., beta-methylstyren

291 The metathesis activity toward olefins with and without allylic C-H groups, namely beta

292 he reactions of readily accessible feedstock olefins with beta-nitrostyrenes by ozone/Fe(II) -mediate

293 allows for rapid access to tetrasubstituted olefins with full stereocontrol.

294 f electron-rich acyclic and tensioned cyclic olefins with heterobiaryls is described.

295 ally competent to perform the epoxidation of olefins with high stereo- and regioselectivity.

296 alyst-mediated copolymerization of non-polar olefins with polar comonomers represents the seemingly m

297 ully used in the asymmetric hydrogenation of olefins with poorly coordinative or noncoordinative grou

298 ti-Markovnikov hydroamination of unactivated olefins with primary alkyl amines to selectively furnish

299 es for the catalytic epoxidation reaction of olefins with the help of hydroperoxides has also been ex

300 lytic system that hydroalkylates unactivated olefins with unactivated alkyl halides, yielding aliphat

301 union of allenes, dienes, styrenes and other olefins, with imines, nitriles and related C-N electroph