ライフサイエンスコーパス: tertiary amine

1 ups (i.e., phenylureas, tertiary amides, and tertiary amines).

2 for a sacrificial electron donor, usually a tertiary amine.

3 noline and aporphine substrates possessing a tertiary amine.

4 d formation was driven by the oxidation of a tertiary amine.

5 tion of a variety of primary, secondary, and tertiary amines.

6 thoxycarbonyl)isocyanate upon treatment with tertiary amines.

7 the slow nitrosation rates hypothesized for tertiary amines.

8 d the formation of NDMA by chloramination of tertiary amines.

9 e design of a series of substituted N-phenyl tertiary amines.

10 reaction with feedstock carboxylic acids and tertiary amines.

11 with about 60% of drug candidates containing tertiary amines.

12 hols, alcohol-acids, as well as reduction to tertiary amines.

13 umber of enantioselective syntheses of alpha-tertiary amines.

14 iterative approach to access functionalized tertiary amines.

15 alcohols and N-hydroxylamine esters to form tertiary amines.

16 amines to afford alpha-trisubstituted-alpha-tertiary amines.

17 r the synthesis of N-alkylated secondary and tertiary amines.

18 one-pot synthesis of 1,2- and 1,3-oxygenated tertiary amines.

19 alkane products allows rapid access to alpha-tertiary amines.

20 ation reactions during chloramination of the tertiary amines.

21 elective palladium-catalyzed alkenylation of tertiary amines.

22 achieved from the appropriately substituted tertiary amines.

23 e synthesis of enantioenriched secondary and tertiary amines.

24 complete reduction to give the corresponding tertiary amines.

25 y binding hot spot, preferably binding small tertiary amines.

26 egy for the streamlined synthesis of complex tertiary amines.

27 on does not exhibit the ordinary basicity of tertiary amines; 3 can be extracted from acidic media wi

28 the enantiomers of 3b and the corresponding tertiary amine 33b revealed that the eutomers are (2S,6S

29 difications to the head group containing the tertiary amine, a tail group that extends away from this

30 With tertiary amines, a >2-order of magnitude decrease in k(H

31 With Lewis basic C-H donors such as THF and tertiary amines, a decrease in k(H) with increasing Lewi

32 For tertiary amines, a moderate rate of abatement was observ

33 In contrast, tertiary amine adds reversibly to S1, because nitrogen c

34 ocycle, and a late-stage installation of the tertiary amine-aldehyde proximity interaction.

35 , sugar, hydroxyl, thiophene, sulfur, azide, tertiary amines, alkyne, vinyl, or phosphonate groups we

36 P attachment, and simultaneously incorporate tertiary amines along with carboxyl and/or hydroxyl grou

37 The ligands contain a tertiary amine, an amino acid side chain, and a carbamat

38 A series of tertiary amine analogs of 3 were synthesized and assayed

39 lic substitution reaction between the parent tertiary amine and a novel derivatizing reagent, di-tert

40 With a balanced composition of tertiary amine and carboxylic acid groups, these nanopar

41 (ii) downstream protoberberines containing a tertiary amine and forming quaternary intermediates dest

42 A number of tertiary amine and quaternary ammonium cations spanning

43 lines that were not affected by the type of tertiary amine and treatment conditions, suggesting that

44 Nitrosatable drugs, such as secondary or tertiary amines and amides, form N-nitroso compounds in

45 bic catalytic protocole (CuI/air) to oxidize tertiary amines and benzylic CH's in drugs.

46 ccompanied by the pyramidal inversion of the tertiary amines and by the rotation of the tribenzylamin

47 The reaction is catalyzed by tertiary amines and can occur with diastereoselectivity

48 by primary and secondary amines, but not by tertiary amines and carbonate buffer.

49 ion of wastewaters impacted by anthropogenic tertiary amines and containing bromide ion.

50 permits iterative alkyl group transfer from tertiary amines and demonstrates a deaminative strategy

51 compounds, including primary, secondary, and tertiary amines and quaternary ammonium compounds, all s

52 Interestingly, UGT activity toward tertiary amines and some steroid hormones was equal.

53 group, with the highest clearance rates for tertiary amines and sulfates and no clearance of QACs.

54 e photochemical mechanisms of coumarin-caged tertiary amines and then optimize the major pathway usin

55 ters, amides, ethers, acetals, nitriles, and tertiary amines and, therefore, should be applicable to

56 in k(H) was observed going from secondary to tertiary amines and, with tertiary amines, on increasing

57 in total) observed was between surfactants (tertiary amines) and endogenous metabolites (fatty acid

58 strongly ionized bases (primary, secondary, tertiary amines), and a pair of quaternary ammonium comp

59 to their functional group (secondary amine, tertiary amine, and amide).

60 g group except for sterically hindered alpha-tertiary amines, and a practical catalytic system for C(

61 ssed along the C(3) axis passing through the tertiary amines, and the two tribenzylamine platforms ar

62 commercially available N-methyl substituted tertiary amines, and therefore it represents an attracti

63 e MAO-N-D5 variant, which is able to oxidise tertiary amines, appear to influence the active-site env

64 To elaborate on this promise, tertiary amines are attached nearby.

65 st, a broad range of alkylated secondary and tertiary amines are obtained in good to excellent yields

66 ntermediates resulting from the oxidation of tertiary amines are trapped during the photoinduced elec

67 -dimethyl 5-HT, in which the side chain is a tertiary amine, are found in the computational simulatio

68 Interaction of the tertiary amines, arecolone, eserine (physostigmine), (+)

69 The use of a tertiary amine as an allosteric effector also enabled a

70 and aryl triflates that uses a weak, soluble tertiary amine as base.

71 Functioning of the C2 tertiary amine as latent reactive group on thiazolidinon

72 tetraketones using cyclic-1,3-diketones and tertiary amines as alkyl synthons under 18 W blue LED ha

73 n the application of primary, secondary, and tertiary amines as efficient organocatalysts for the de

74 es, which is the first example of the use of tertiary amines as intermolecular nucleophiles in metal-

75 ly meta-selective C-H arylation using simple tertiary amines as the directing group.

76 Different tertiary amines as well as aryl iodides have been examin

77 ocyclic and aliphatic primary, secondary and tertiary amines as well as N-methylamines and more compl

78 a, select protonated primary, secondary, and tertiary amines as well as tetramethylammonium with 19-2

79 Direct C-H vinylations of N-aryl tertiary amines, as well as decarboxylative vinylations

80 The selective sp(3) C-N bond activation of tertiary amines at the less steric side using O2 as a so

81 We examined primary, secondary, and tertiary amines at various pHs.

82 The addition of tertiary amine base is found to dramatically accelerate

83 Calcium salts and a tertiary amine base promote the reaction with high site-

84 1 with primary alcohols in the presence of a tertiary amine base results in salts of intact TriMP alk

85 vation through the Lewis acid and a tethered tertiary amine base.

86 in the presence of potassium carbonate or a tertiary amine base.

87 A squaramide-containing tertiary amine based bifunctional organocatalyst efficie

88 enewable sources, we synthesized a series of tertiary amine-based ILs from aromatic aldehydes derived

89 We report the synthesis of 46 tertiary amine-bearing N-alkylated benzo[d]imidazol-2(3H

90 on of metal-organic framework materials with tertiary amine-binding sites.

91 step in the intramolecular C-H borylation of tertiary amine boranes activated with catalytic amounts

92 an extended structure containing a terminal tertiary amine, but this had no beneficial effects on bi

93 he iminium ion, which is then reduced to the tertiary amine by Et(2)SiH(2).

94 tudied for releasing primary, secondary, and tertiary amines by direct photochemical breaking of the

95 recurring events: the in situ methylation of tertiary amines by PO(OMe)(3), Ni-catalyzed C-N bond cle

96 rimary amines--over branched, secondary, and tertiary amines--by a two-step process involving a proto

97 lutamate using aqueous hydrogen peroxide and tertiary amine catalysis.

98 Tertiary amine catalysts are essential components in man

99 stand design principles how the structure of tertiary amine catalysts having N, N-dimethyl groups can

100 ong-range electron-transfer oxidation of the tertiary amine center by the HRP oxidants.

101 ntrol (7) revealed that the presence of a N1 tertiary amine center imparted a significant reduction i

102 al complexation process, it is proposed that tertiary amine compounds, having N-substituents which ar

103 -stage lithiation-borylation reaction with a tertiary amine containing carbenoid.

104 Tertiary amine containing poly(propyleneimine) second (G

105 We report the development of a tertiary amine-containing beta-turn peptide that catalyz

106 The library consisted of dialkyl tertiary amine-containing commercially available pharmac

107 a model compound (quinuclidine) and to three tertiary amine-containing drugs (cinnarizine, loxapine,

108 ion while olefins undergo aziridination, and tertiary amine-containing natural products are converted

109 analysis, we describe herein a new series of tertiary amine-containing pyrazolones and their structur

110 Studies with a tertiary-amine-containing antibiotic show that the resul

111 rbamate bond; however, the ability to employ tertiary-amine-containing bioactive molecules has been e

112 ino)ferrocene (DPPF) in combination with the tertiary amine Cy(2)NMe proved effective in the olefinat

113 tions this happens even if the corresponding tertiary amine (DDMA) is added, instead of DDMA-Br.

114 aternary ammonium compound clofilium and its tertiary amine derivative LY97241 were used to analyze m

115 a route to synthesize valuable chiral alpha-tertiary amines directly from an isomeric mixture of alk

116 easily accessible a-silyl amine reagents or tertiary amines directly, secondary and tertiary amine m

117 (N(4)S(thiolate))Fe(II) complex, containing tertiary amine donors, [Fe(II)(Me(4)[15]aneN(4))(SPh)]BP

118 sed photolabile groups could be used to cage tertiary amine drugs as quaternary ammonium salts.

119 NDMA formation from the most reactive tertiary amines (e.g., dimethylaminomethylfurfuryl alcoh

120 Increased positive charge at the tertiary amine end of tetracaine results in higher poten

121 Previous examples have principally been tertiary amines, especially those with cyclic scaffolds.

122 Diverse arrays of tertiary amines first undergo reductive quenching of exc

123 active group, a quinoline fluorophore, and a tertiary amine for enhancing ESI+ MS ionization.

124 tin, and ferric TRENCAM, which substitutes a tertiary amine for the macrocyclic lactone ring of ferri

125 CI: 1.40, 2.73); odds ratios associated with tertiary amines from the lowest tertile of nitrite intak

126 leton, hexamethylindotricarbocyanine, with a tertiary amine functionality that was electronically cou

127 In contrast to prior works employing a tertiary amine functionality, a weakly BrOnsted-basic am

128 tones; however, the direct polymerization of tertiary amine functionalized cyclic esters has remained

129 ines to give the corresponding secondary and tertiary amines generally in high yields (up to 96%) and

130 hat in the presence of a proton source and a tertiary amine generates the corresponding alpha-difluor

131 heterocycles like azaacene and secondary and tertiary amines give exclusively the dyes containing a t

132 Using a cationic tertiary amine gradient, anionic molecules were directio

133 g the water solubility of drugs containing a tertiary amine group are reported.

134 metal-organic framework functionalized with tertiary amine groups that exhibits high capacities for

135 n alkylating agent, to convert polymer-bound tertiary amine groups to less chloramine-reactive quater

136 of the oppositely charged paper (protonated tertiary amine groups) and the anionic groups of the rea

137 erionic compounds with hydrocarbon ester and tertiary amine groups, the bulk polymer itself is elasto

138 tivity lower than that of the compounds with tertiary amine groups.

139 in the order: secondary amines approximately tertiary amines >> primary amines.

140 o-catecholato) with equimolar AlCl(3) and a tertiary amine has been applied to a wide range of arene

141 o nitrosatable drugs, including secondary or tertiary amines, has been associated with preterm birth.

142 molecular C-H functionalization reactions of tertiary amines have been developed.

143 optimal temperature, affording chiral alpha-tertiary amines in excellent yields with high enantiocon

144 provides high yields in methanol, release of tertiary amines in MeCN/water can improve yields and red

145 .) are reported for several hydrocarbons and tertiary amines in solution.

146 en investigated by chloramination of several tertiary amines in the absence and presence of bromide i

147 Upon protonation of the tertiary amines in the dendritic interior, binding becam

148 esters react with heteroaromatic and certain tertiary amines in the presence of an oxidant (I(2)) to

149 S zwitterions (two carboxyl betaines and two tertiary amines) in aerobic soils.

150 trosatable drugs, particularly secondary and tertiary amines, in conjunction with higher levels of di

151 A range variety of tertiary amines including N-arylamines and N-alkylamine

152 f linear and branched primary, secondary and tertiary amines including N-methylamines and molecules u

153 ing a broad range of alkylated secondary and tertiary amines, including fluoroalkyl-substituted anili

154 y gold catalysis without the purification of tertiary amine intermediates.

155 displacement of a methyl group attached to a tertiary amine is a reaction without an obvious preceden

156 atalyzed alpha-C-H bond functionalization of tertiary amines is presented.

157 , and L-proline), but N,N-dimethylglycine, a tertiary amine, is not a substrate.

158 Nitrosation of MDEA, a tertiary amine, is not catalyzed by the addition of CO2

159 HAS polymers possess primary, secondary, and tertiary amines, leading to multiple chemisorption react

160 ty of 14 and why converting the secondary to tertiary amine leads to enhanced selectivity.

161 quenching of the Ir(3+) excited state by the tertiary amine leads to the ammonium radical cation, wit

162 eaction of both acyclic and cyclic aliphatic tertiary amines led to the formation of 2- N, N-dialkyla

163 tions of copper(II) bromide and an aliphatic tertiary amine ligand (Me6-Tren; Tren = tris(2-aminoethy

164 ows the construction of stable secondary and tertiary amine-linked protein conjugates without affecti

165 itine binding is inhibited by bupivacaine, a tertiary amine local anesthetic.

166 The use of the tertiary amine matrix solution permits the simultaneous

167 rapping reagent and an exquisitely selective tertiary amine-mediated hydrogen-atom abstraction at the

168 nol (AMP) and monoethanolamine (MEA) and the tertiary amine methyldiethanolamine (MDEA).

169 argensis was able to biotransform two of the tertiary amines, mianserin (MIA) and ranitidine (RAN), e

170 odifiers without amine groups nor those with tertiary amine moieties are capable of adsorbing on the

171 s or tertiary amines directly, secondary and tertiary amine moieties can be installed onto monoaryl a

172 structurally diverse primary, secondary, and tertiary amine moieties.

173 , the 9-aza-APs carrying a distal lipophilic tertiary amine moiety in both chains were capable of ove

174 could be explained by the speciation of the tertiary amine moiety of TRA, with apparent second-order

175 ) cage contains 12 amide NH groups plus four tertiary amine N groups, the latter of which are positio

176 rein, we demonstrate for the first time that tertiary amine N-oxides, an oxidative degradation produc

177 approach to the characterization of dialkyl tertiary amine-N-oxides is presented.

178 form through diagnostic losses from dialkyl tertiary amine-N-oxides.

179 s location in the membrane placed the drug's tertiary amine near the phosphate of the headgroup, its

180 t method for accessing N-aryl alpha-branched tertiary amines, new catalysts have been designed to sup

181 Interestingly, the tertiary amine nicotine dramatically enhances uracil chl

182 f a "crypt" that contains eight nonreducible tertiary amine nitrogens.

183 Here we report that tertiary amine nucleophiles show excellent C-2 selectivi

184 likely than were control women to have taken tertiary amines (odds ratio = 1.60, 95% confidence inter

185 es that MeTr decreases the acidity of the N5 tertiary amine of CH3-H4folate by 1 pK unit in both wate

186 mechanism in which both the thiourea and the tertiary amine of the catalyst are involved productively

187 ate first, by the action of the quinuclidine tertiary amine of the cinchona catalyst on MK.

188 strong charge-charge interaction between the tertiary amine of the ligand and an aspartic acid residu

189 tituted benzene rings linked directly to the tertiary amine of the saturated heterocycle.

190 of the terminal primary amines and interior tertiary amines of the dendrimer structures.

191 the terminal primary amines and the interior tertiary amines of the dendrimers to the observed EMF re

192 The dimers, in which the tertiary amines of the lidocaine moieties are linked by

193 sitive to negative greatly shifts the pKa of tertiary amines of the PAMAM dendrimer interior.

194 are selective blockers of 5HT reuptake, and tertiary amines of the trans compounds are less potent t

195 The (13)C chemical shifts of six tertiary amines of unambiguous conformational structure

196 ted and experimental (13)C shifts of the six tertiary amines of unambiguous structure are found.

197 tive reveals that the positive charge of the tertiary amine on the trienyl arm induces G selectivity.

198 from secondary to tertiary amines and, with tertiary amines, on increasing steric hindrance at nitro

199 l exposure to NSDs containing a secondary or tertiary amine or amide.

200 ators of cholinesterases (ChEs) that contain tertiary amine or imidazole protonatable functional grou

201 ive aldol reactions realized by using either tertiary amines or a dizinc aldol catalyst constitute tw

202 talyst, provides a direct synthesis of alpha-tertiary amines, or their corresponding gamma-lactams.

203 polymer bearing a seven-membered ring with a tertiary amine (PC7A)-activates innate-immunity pathways

204 surfactants containing both zwitterionic and tertiary amine pendent groups were synthesized for stabi

205 It has been shown for selected tertiary amine pharmaceuticals that they react with ozon

206 A tertiary amine POC (6FT-RCC3) demonstrated very high SO(

207 Mechanistic investigation revealed that tertiary amines predominately operate as Bronsted rather

208 Certain tertiary amine products generated through this method ar

209 electivities are observed for secondary over tertiary amine products, even though the secondary amine

210 ned syntheses of complex ether, sulfone, and tertiary amine products, some of which would be difficul

211 dendrimers have a significant percentage of tertiary amines protonated, approximately 30%.

212 hydroxide, ammonia, primary, secondary, and tertiary amines provide evidence that carbamate, rather

213 These results indicate that tertiary amine pyrazolones comprise a valuable class of

214 ch proved fully operative in the presence of tertiary amines, quinoline, and other Lewis basic sites.

215 Tertiary amines react rapidly and reversibly with arylke

216 However, the synthesis of tertiary amines remains a significant challenge due to t

217 to access various a- and B-boron-substituted tertiary amines, respectively, from common secondary ami

218 e DCA-loaded compound 10, characterized by a tertiary amine scaffold, because it exhibited enhanced (

219 n with melamine acetaldehyde, resulting in a tertiary amine side chain that affords both peptide solu

220 cated that 4-substituted amino groups with a tertiary amine side chain, such as chloroquine, were ass

221 Here, bulky, chiral tertiary amine side chains were incorporated into polype

222 Additionally, the tertiary amine side chains, as widely used functional gr

223 and the length of the tether connecting the tertiary amine site used for ionization via protonation

224 he combustion products in a 5% water-soluble tertiary amine solution.

225 y simple and highly efficient C(2)-symmetric tertiary amine-squaramide organocatalyst for asymmetric

226 c and experimental data strongly suggest the tertiary amine-stabilized dichlorosilylene to be the mos

227 amino acids), but not from secondary amines, tertiary amines, sterically hindered primary amines, or

228 eaction conditions, with good generality for tertiary amine structure and moderate to excellent yield

229 Additionally, of all the tertiary amines studied to catalyze the reaction, the be

230 In several cases of tertiary amines subject to rapid exchange, where experim

231 e H(8)BINOL-AM compounds containing 3,3'-bis-tertiary amine substituents are synthesized by using a o

232 ine-amide-dithiol (AADT) chelates containing tertiary amine substituents as small-molecule probes for

233 ine-amide-dithiol (AADT) chelates containing tertiary amine substituents were synthesized and shown t

234 igated, and differences in the reactivity of tertiary amine substrates are discussed.

235 cidic complex, 1H-1,2,3-benzotriazole, and a tertiary amine such as DBU.

236 in the dark in the presence of an excess of tertiary amines, such as tris[2-(dimethylamino)ethyl]ami

237 loying a series of sterically differentiated tertiary amines suggest that the steric nature of the am

238 Three classes of Lewis bases-tertiary amines, sulfides, and selenophosphoramides-were

239 for a switchable cationic surfactant, e.g., tertiary amine surfactant (Ethomeen C12), is 2.22% in DI

240 philic imine allylation strategies for alpha-tertiary amine synthesis.

241 Herein, we report tertiary amine (TA)-modified resin adhesives (TA@RAs) wi

242 affold types, one a bicyclic iodo-vinylidene tertiary amine/tertiary alcohol and the other, a spirocy

243 Sibutramine is a tertiary amine that has been shown to induce dose-depend

244 ral helical (thio)urea oligomer and a simple tertiary amine that is able to promote the Michael react

245 catalyst is a simple tetrapeptide bearing a tertiary amine that may function as a Bronsted base.

246 explains the capsule's high affinity toward tertiary amines that are protonated and therefore encoun

247 (CSIA) of NDMA during chloramination of four tertiary amines that produce NDMA at high yields, namely

248 itiated electron transfer from a sacrificial tertiary amine, the reduced intermediate of complexes co

249 For gel-entrapped Ru(bpy)3 2-/tertiary amines, the shape and intensity of the ECL-pote

250 ctional chiral phosphines or multifunctional tertiary amine-thioureas as the catalyst, respectively.

251 ary amides from aryl boronic acids and inert tertiary amines through the oxidative carbonylation via

252 ion of the catalyst, which is reduced by the tertiary amine to produce the single-electron reducing a

253 d by photoinduced electron transfer from the tertiary amine to the Bodipy excited state.

254 t are trapped in the presence of co-oxidized tertiary amines to form alpha-amino nitriles.

255 lex natural products containing nucleophilic tertiary amines to generate a C-C bond.

256 effective for the dehydrogenation of simple tertiary amines to give enamines than the previously rep

257 hydrogenation of several beta-functionalized tertiary amines to give the corresponding 1,2-difunction

258 The photocycloaddition of tertiary amines to inverted question mark60fullerene (C(

259 The synthetic utility of tertiary amines to oxidatively generate alpha-amino radi

260 queous mixtures of commonly used primary and tertiary amines to study the influence of the different

261 ts oxidative N-dealkylation/carbonylation of tertiary amines to tertiary amides by using molecular ox

262 strated (conversion to quaternary centers, C-tertiary amines) together with application of the method

263 For secondary and tertiary amines, total N-nitrosamine formation under the

264 s, are rapidly and quantitatively reduced to tertiary amines under mild conditions with low catalyst

265 osition of alpha-diazo carbonyls tethered to tertiary amines underwent a benzylic Stevens [1,2]-rearr

266 The adjusted hazard ratios for tertiary amine use in the third trimester by increasing

267 s were converted into tertiary alcohols or C-tertiary amines using chloramine.

268 oped for the synthesis of a diverse range of tertiary amines using inexpensive polymethylhydrosiloxan

269 romotes the alpha-cyanation of secondary and tertiary amines using magnetic nano-ferrites.

270 eneral method for the difluoromethylation of tertiary amines, using diethyl bromodifluoromethylphosph

271 en-deuterium exchange of biologically active tertiary amines utilizing the borrowing hydrogen methodo

272 substituents, the alkyl chain length and the tertiary amine was conducted.

273 ylation of primary and secondary amines into tertiary amines was confirmed by FTIR and NMR analysis.

274 the thermal decay of sterically overcrowded tertiary amines was not promoted by bases.

275 tions, a range of both cyclic and open chain tertiary amines was tested as substrates, resulting in y

276 tems for the chloramination of secondary and tertiary amines, we investigated the kinetics of precurs

277 Chloropicrin yields from tertiary amines were low.

278 aryl sulfonamides, while bulky secondary and tertiary amines were preferred at the benzylic amine pos

279 uring the first minutes of the reaction when tertiary amines were present.

280 monium salts, derived from alkyl halides and tertiary amines, were the intermediates to yield thioest

281 ive deracemisation of primary, secondary and tertiary amines when used as part of a chemoenzymatic ox

282 ydroamination to furnish the enantioenriched tertiary amine, whereby enantioinduction occurs through

283 rovide perdeuterated primary, secondary, and tertiary amines, which are difficult to achieve via othe

284 facilitated the synthesis of alpha-trialkyl tertiary amines, which cannot be accessed via CRA.

285 onally and structurally diverse a-trialkyl-a-tertiary amines, which makes use of three readily availa

286 tion (HER), we studied the substitution of a tertiary amine with a softer pyridine group and the incl

287 nt yield from the reaction of a secondary or tertiary amine with o-iodoxybenzoic acid (IBX) or o-iodo

288 The unprecedented reaction of tertiary amines with 2(3 H)-benzoxazolones has been inve

289 tive synthesis of sterically demanding alpha-tertiary amines with a tetrasubstituted carbon stereocen

290 the catalytic asymmetric alpha-acylation of tertiary amines with aldehydes facilitated by the combin

291 ation of various aliphatic as well as cyclic tertiary amines with alkynes has been described.

292 p(3))-H bonds adjacent to a nitrogen atom of tertiary amines with alkynyl bromides as radical alkynyl

293 ications are typically achieved by employing tertiary amines with catalytically active N, N-dimethyl

294 The mechanism directly couples tertiary amines with cyanoaromatics by using mild and op

295 t cross-dehydrogenative coupling of aromatic tertiary amines with isocyanides and water leads to amid

296 In general, secondary amines or tertiary amines with nonsterically demanding substituent

297 Blends of tertiary amines with piperazine (PZ) showed n-nitrosopip

298 ing substituents on nitrogen are superior to tertiary amines with sterically demanding substituents o

299 Mn-catalyzed reduction of tertiary amides to tertiary amines, with a useful scope, is demonstrated fo

300 metal-free and modular transformation forms tertiary amines, without structural constraint, via the