ライフサイエンスコーパス: amine

1 mide bond formation from carboxylic acid and amine.

2 rovide 2 equiv of the corresponding aromatic amine.

3 alpha-functionalization of cyclic secondary amines.

4 ted amidation activity for various acids and amines.

5 ctions during chloramination of the tertiary amines.

6 e analyzed samples were positive in aromatic amines.

7 nation of 1,3-dienes to generate homoallylic amines.

8 es, and provides access to valuable benzylic amines.

9 a possible link to the presence of aromatic amines.

10 n-coupled receptor bound by endogenous trace amines.

11 mportant methods for the synthesis of chiral amines.

12 palladium-catalyzed alkenylation of tertiary amines.

13 erse array of functionalized enantioenriched amines.

14 trogen, including low molecular weight alkyl-amines.

15 erance with a range of primary and secondary amines.

16 ends on the ring size of the starting cyclic amines.

17 e of many of the common interfering biogenic amines.

18 th alpha-halocarbonyls and aryl or aliphatic amines.

19 le catalyzed kinetic resolution of aliphatic amines.

20 ) catalyses oxidative deamination of primary amines.

21 2 insertion into the alpha-C-H sigma-bond of amine 1a.

22 including the two potent mutagenic aromatic amines 2,3- and 2,8-phenazinediamine, which were reporte

23 for simultaneously quantifying nine biogenic amines, 21 amino acids, and ammonium ions, in beer.

24 tively, whereas 8,9-disubstituted-9H-purin-6-amines 27-31 and 6-imino-8,9-disubstituted-6,9-dihydro-1

25 ibofuranosyl)-6-imino-1,6-dihydropyrimidin-4-amines 3 or 4-(N-ribofuranosyl)-6-aminopyrimidines 4 via

26 ino-8,9-disubstituted-6,9-dihydro-1H-purin-1-amines 32-33 were obtained in two steps using formamide

27 The exception is amine 4 that undergoes excited-state intramolecular prot

28 re accessible in three steps from commercial amines (50-85%).

29 -(quinolin-8-yl)-1H-pyrazol-5-yl)pyridazin-3-amine (69).

30 eV, 6: 7112.4 eV) as compared with a ferrous amine adduct ((Ar)L)FeCl(NH2Ad) (7: 7110.3 eV).

31 pecific strain-release "cyclopentylation" of amines, alcohols, thiols, carboxylic acids, and other he

32 e reaction has a broad scope in terms of its amine, aldehyde, and isocyanide nature.

33 Aryl amines also combine with Cu(2+) and NADPH to form reacti

34 tabolites, including sphingolipids, biogenic amines, amino acids and urea.

35 henylpyrimidin-2-yl)[2-(2-pyridylamino)ethyl]amine analogues which are inhibitors of human glycogen s

36 that is based on the condensation between an amine and a carbonyl compound.

37 covered by Hugo Schiff, condensation between amine and aldehyde represents one of the most ubiquitous

38 te stage sequential functionalization of the amine and amide nitrogens to rapidly produce diverse ana

39 Schiff-base condensation between an amine and an aldehyde is one of the most common reaction

40 teraction between the pseudopilin N-terminal amine and E5 to limit polar interactions with membrane p

41 orbent, and chemical structure of the parent amine and nitrosamine.

42 ation, overcoming long-standing and unsolved amine and organoboron limitations of this valuable trans

43 ff-cycle inhibitory processes, the source of amine and organoboron reactivity issues, and the origin

44 plore how two nonionic polar groups (primary amine and primary amide) influence hydrophobic interacti

45 ycol generating, after condensation with the amine and tautomeric equilibrium, the corresponding pyrr

46 le is activated by the catalyst's protonated amine and that the nucleophile binds to the thiourea moi

47 t restraints on their tertiary or quaternary amine and their distance to an ester or related center.

48 The addition of amine and thiol linkers have shown a significant effect

49 at were not affected by the type of tertiary amine and treatment conditions, suggesting that the obse

50 we have identified novel N-methyl-containing amines and amides, primary amides, and novel N-acetylate

51 that methanesulfonic acid (MSA) reacts with amines and ammonia to form particles, which is expected

52 ibility of this reaction with secondary free amines and anilines also overcomes the limitations of pa

53 s known to biotransform in soils to aromatic amines and azo-dimers, it is seldom mineralized by indig

54 t reaction between o-nitrochalcones, primary amines and beta-dicarbonyl compounds in the presence of

55 ethod for the oxidation of benzylic carbons (amines and cyanides) into corresponding benzamides using

56 roducts could be reduced to give spirocyclic amines and diamines.

57 chiral lipophilic and conformationally rigid amines and heterocycles by decarboxylation of adamantane

58 base)borylene adducts are isoelectronic with amines and phosphines.

59 r was further tested with different biogenic amines and ratiometric response was obtained for tyramin

60 are formed upon bonding of CO2 with surface amines and readily released from the surface by pressure

61 The formation of bioactive amines and their changes in cocoa beans during seven day

62 olite of diallyl monosulfide, alkylates both amines and thiols under physiologically relevant conditi

63 i) high contents of spermine, total biogenic amines and total polyamines; and iii) the highest spermi

64 e prereaction of the catalyst, aldehyde, and amine, and instead, the diazo compound could be added di

65 sical properties of nitrosamines, the parent amine, and the influence of the physical properties of t

66 tween 0.03mg/L and 0.63mg/L for the biogenic amines, and 0.05mg/L and 5.19mg/L for other compounds.

67 the intermediate organoboranes to alcohols, amines, and alkenes.

68 idines from azirine-2-carbaldehydes, primary amines, and diazo carbonyl compounds under Rh(II) cataly

69 icomponent trans-aziridination of aldehydes, amines, and diazo compounds with BOROX catalysts is deve

70 of structurally diverse beta-ketoenols with amines, and use it to prepare novel two-dimensional (2D)

71 hael addition of ethenesulfonyl fluoride and amines/anilines while the BB monomers were obtained from

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

73 ines, including amino acids and more complex amines are competent coupling partners.

74 Biogenic amines are conserved signaling molecules that link food

75 Amines are recognized as key compounds in new particle f

76 Cyclic amines are ubiquitous core structures of bioactive natur

77 hat are most likely to accumulate contain an amine, are amphiphilic and rigid, and have low globulari

78 ation, beta-aminoalkylation, dehalogenation, amine arylation, and decarboxylative radical formation).

79 protonated species (CI)H(+) using protonated amines as reagent ions.

80 Trace amine-associated receptor 1 (TAAR1) agonists have been s

81 Trace amine-associated receptor 1 (TAAR1) is a highly conserve

82 As partial agonists at trace amine-associated receptor 1 (TAAR1) promote wakefulness

83 As a result, we found 5H-purin-6-amine at 1 microg/mL, originated from Sedum sarmentosum,

84 tep was found to be more facile with smaller amines at the expense of a more difficult dissociation o

85 a wide range of amines, which include ethyl amines, azetidines, pyrrolidines, piperidines, azepanes,

86 aimed to assess lipid oxidation and biogenic amine (BA) development in "muxama", a dry-cured tuna mus

87 Tyramine and histamine are the biogenic amines (BA) most commonly found at high concentrations i

88 amines suggest that the steric nature of the amine base additive exerts a significant influence on th

89 Amine-based absorption is the primary contender for post

90 as a carbamate serves as the CO2 carrier for amine-based capture strategies.

91 NH2 as a highly reactive and stereoselective amine-based catalyst that allows C-C bond formations to

92 pH halts dichloramine formation, it converts amine-based NDMA precursors to their more reactive, neut

93 e aspartic protease inhibitor hydroxyl-ethyl-amine-based scaffold compound 49c.

94 ient of many disinfectants-to benzyldimethyl amine (BDMA) was identified in the genome of Pseudomonas

95 Complex amines bearing a C horizontal lineC double bond and dist

96 al-organic framework materials with tertiary amine-binding sites.

97 e and reversible insertion of CO2 into metal-amine bonds to form ammonium carbamate chains.

98 Moreover, a secondary amine building block that contains all carbon atoms of t

99 n be derivatized to afford a range of chiral amine building blocks incorporating motifs readily encou

100 tegy for the synthesis of high-value allylic amine building blocks that does not require the use of t

101 Although the alkylation of an amine by an alkyl halide serves as a "textbook example"

102 , the selective mono-alkylation of aliphatic amines by unactivated, hindered halides persists as a la

103 n reaction whereas both the aldehyde and the amine can possess a wide range of structural and electro

104 A further 33 biogenic amines can be monitored in samples for relative changes

105 mide product directly into the corresponding amine, carbamate, and urea.

106 ial aldolase RA95.5-8, for example, exploits amine catalysis to promote mechanistically diverse carbo

107 A simple secondary amine catalyst, 2-methyl-l-proline, and its tetrabutylam

108 reaction development was the use of a chiral amine catalyst, bearing a redox-active carbazole unit, w

109 The enantioselectivity of amine-catalyzed reactions of aldehydes with electrophile

110 mic DNA that readily undergo spontaneous and amine-catalyzed strand cleavage reactions that generate

111 interaction between tryptophan (Trp) and an amine cation are shown to absorb and fluoresce in the vi

112 ment of small interfering RNA-releasing poly(amine-co-ester) nanoparticles, distinguished by their hi

113 Alcohol-amine combinations are discussed to the extent that net

114 tructural effects of these two key principal amine compounds imposed by hydrogen bonding to water, wh

115 cond, we investigated the distribution of 12 amine-containing and eight control micropollutants in bo

116 nes, phenethylamines and phenylpropylamines; amine-containing building blocks of great utility in man

117 hat it is an important removal mechanism for amine-containing micropollutants in batch experiments wi

118 ulk heterojunction polymeric films, in which amine-containing polymers were mixed in the solution use

119 The compounds incorporate 13 different amine-containing side chains designed to bind in the min

120 wed that germ cells cultured with 5H-purin-6-amine could maintain their stable characteristics.

121 C-H functionalization, the use of aliphatic amine coupling partners is limited.

122 H2, Mo hydride complexes bearing protonated amines, [CpMo(H)(CO)(P2N2H)](+), were characterized by s

123 a range of nucleophiles including hydrides, amines, cyanide, and protected enolates.

124 estinal concentrations of SCFAs and biogenic amines decreased with the dietary protein reduction.

125 adiation (365 nm) in the presence of various amines depending on the solvent.

126 ions that enable stereoselective addition of amine derivatives and alcohols onto pendant unactivated

127 ies of 4-thiazol-N-(pyridin-2-yl)pyrimidin-2-amine derivatives as highly potent and selective inhibit

128 rongly favored over N-oxidation for numerous amine derivatives.

129 amido-Ir-coordinated alkene by the exogenous amine determine the outcome of the reaction.

130 ecarboxylase (AADC), which synthesizes trace amines directly from dietary amino acids (such as trypto

131 Whereas amine donors react with O2-chemisorbed AC and nucleophil

132 catalyst, an iridium photosensitizer, and an amine electron donor, is capable of coupling halocarbons

133 The use of amine end-capped polyynes as precursors to substituted p

134 ntaining the CNCs into a toluene solution of amine end-functionalized polystyrene are completely supp

135 ly important in the case of (hetero)aromatic amines-essentially a one-pot reaction with no isolation

136 ion is highly selective for the alpha-C-H of amines, ethers and sulphides, which are commonly found i

137 owing to its capability to label the primary amines exposed on protein surface, but also could be app

138 cal and microbiological parameters, biogenic amines, fatty acids and texture profiles and sensory pan

139 al condensation of aryl isothiocyanates with amines followed by dehydrosulfurization and guanylation

140 er to access a variety of useful homoallylic amines from simple commercially available starting mater

141 he molecular pathways through which biogenic amines function in model organisms may improve our under

142 ification of carbon electrodes with carboxyl-amine functionalities offers protection against formatio

143 he proposed biosensor by copolymerization of amine functionalized monomer, which is indispensable to

144 proved in situ membrane healing method using amine-functionalized silica microparticles that is effec

145 In contrast to other primary amine-functionalized solid adsorbents that uptake CO2 pr

146 donating phosphine ligand and the most basic amine functions performs best among the series, with tur

147 N-methylation of the N-terminal amine further limited its interactions with phospholipid

148 This finding suggests that replacing an amine group (K side chain) with a primary amide group (Q

149 ers an acyl chain from a phospholipid to the amine group of the N-terminal cysteine residue of the ap

150 containing a thiol, a thioether, or an extra amine group such as arginine, cysteine, lysine, methioni

151 First, interaction of an inhibitor's amine group with the conserved active-site Asp is essent

152 raamide complexes with four appended primary amine groups are measured as a function of pH.

153 ity, large surface area and high fraction of amine groups as aptamer binding sites.

154 similar to that of thiophenol, aniline, and amine groups but not as that of hydroxyl.

155 ffinity to the donor groups (COO(-) and some amine groups in its deprotonated form, NH2) of cysteine

156 functionalized with mixture of carboxyl and amine groups NDandante or amine NDamine, carboxyl NDvox

157 neither naphthalene-based modifiers without amine groups nor those with tertiary amine moieties are

158 In addition, computations indicate that the amine groups shift their pKa values due to the confined

159 ganic framework functionalized with tertiary amine groups that exhibits high capacities for radioacti

160 ompounds with hydrocarbon ester and tertiary amine groups, the bulk polymer itself is elastomeric and

161 onfirmed the surface modification of CNTs by amine groups, whereas dynamic light scattering establish

162 act as a bioisostere of hydroxyl, thiol, or amine groups.

163 ied concerning the formation of heterocyclic amines (HAAs).

164 carboxymethyl cyclohexadienones and primary amines has been developed.

165 tion of methylamine, the simplest methylated amine, have mainly focussed on the fate of the carbon fr

166 In this study, we show four other amine heterocycles: 6-methyl, 5-oxo-2,3,4,5-tetrahydropy

167 is reversed when we replace the thiols with amines, highlighting the impact of metal-S covalent and

168 ed, highlighting the roles of water, CO, and amine in the generation of a more complete catalytic cyc

169 hly efficient for the extraction of aromatic amines in a wide polarity range (log Kow values from -0.

170 Biogenic amines in Canadian pork for the chilled export Japanese

171 l bromide electrophiles and delivers allylic amines in excellent yields (up to 99%).

172 m the corresponding heterocyclic thiols with amines in good to excellent yields.

173 aluation methods aiming to identify aromatic amines in six mutagenic wastewater effluents from a chem

174 Detection limits for aromatic amines in textiles (0.007-2 mg kg(-1)) were well below t

175 cohols, carboxylic acids, and even secondary amines in the substrates.

176 st bearing a PHOX ligand, generating allylic amines in up to 97:3 er.

177 We identified 14 amines including the two potent mutagenic aromatic amine

178 A wide variety of primary amines, including amino acids and more complex amines ar

179 e show that natural monoamines and synthetic amines inhibit pDC activation by RNA viruses.

180 enables the conversion of readily available amines into synthetically valuable aziridines in high en

181 docrine tumours (NETs) can secrete bioactive amines into the bloodstream, causing carcinoid syndrome,

182 acid catalyzed kinetic resolution of primary amines is described that is based on the condensation be

183 The similar influence of other amines is expected based on literature data.

184 Direct oxidation of alpha-CH2 group of free amines is hard to achieve due to the higher reactivity o

185 An amine layer was produced next by modifying the surface w

186 f methylene C-H bonds in secondary aliphatic amines lead to the formation of trans-disubstituted beta

187 or NU 2058 [6-(cyclohexylmethoxy)-9H-purin-2-amine] leads to G1-phase cell cycle arrest in the marine

188 supported by the TPA (tris(pyridyl-2-methyl)amine) ligand family with H2O2/AcOH or AcOOH at -40 degr

189 onstruction of stable secondary and tertiary amine-linked protein conjugates without affecting the st

190 ructure of a new class of concentrated metal-amine liquid, Li-NH3 -MeNH2 , is presented in which the

191 hetized and unilateral injections of dextran-amine made into lumbosacral DRGs (L5-S2).

192 at the aromatic ring of the phenyl aliphatic amines may form cation-pi interaction with the pyridiniu

193 o a kitchen degreaser containing monoethanol amine (MEA).

194 n, alkylation, or glycosylation step with an amine-mediated glycosylation of the boronic ester, a var

195 ding of the covalent interaction of aromatic amine metabolites with protein nucleophiles.

196 Paralleled proteomics and amine metabolomics analyses using mdDiLeu were systemati

197 azido group reacts with H2S to form an aryl amine (MitoN).

198 without amine groups nor those with tertiary amine moieties are capable of adsorbing on the metal sur

199 Primarily, C-dots modified with amine moieties were synthesized using the one-step micro

200 d to achieve due to the higher reactivity of amine moiety.

201 pling between quinoxalinones (sp(2) C-H) and amines (N-H) in the presence of catalytic iodine is repo

202 re of carboxyl and amine groups NDandante or amine NDamine, carboxyl NDvox or hydroxyl groups NDH and

203 Neuromodulators, including biogenic amines, neuropeptides, and hormones, are released to sig

204 says indicate that males likely use biogenic amine neurotransmitters through the nervous system to co

205 Amine neurotransmitters, such as noradrenaline, mediate

206 g from hydrogen atom abstraction from the N6-amine of 2'-deoxyadenosine (dA*).

207 ess this problem, we modified the N-terminal amine of leptin with Pluronic P85 (LepNP85) and administ

208 nted ability to transfer the primary epsilon-amine of lysine to peptidoglycan.

209 sine 5'-phosphosulfate) to the hydroxyls and amines of their scaffolds.

210 vatives containing either a allyl(tert-butyl)amine or a 1,2,3,6-tetrahydropyridine unit in propargyli

211 The resulting amine or heterocycle is then protonated/metalated by the

212 The effects of amine structure, primarily amine order, on nitrosamine formation and the correspond

213 Semicarbazide-sensitive amine oxidase (SSAO) catalyses oxidative deamination of

214 The related copper-containing amine oxidase human vascular adhesion protein-1 also exc

215 that is highly selective over LOX and other amine oxidases.

216 It has been shown for selected tertiary amine pharmaceuticals that they react with ozone and for

217 80 (n = 6) peak pairs or metabolites in the amine/phenol submetabolome from the (12)C-/(13)C-dansyl

218 patterning of ethylene diamine and terminal amine polyethylene glycol chain to prevent non-specific

219 The amines present in these reactions were incorporated into

220 a-substituted five- to seven-membered cyclic amines proceeds very efficiently to provide high control

221 aniline and 4-methoxy-3-nitroaniline, to the amine product 2,4-diaminoanisole.

222 activity that supports full reduction to an amine product in the presence of the convenient and inex

223 lends itself to the use of this motif as an amine protecting/activating group within a broader conte

224 Subsequent amination with a large variety of amines provided the final N-acylguanidines, with the ove

225 ed chain reaction, the oxidation of CPA 1 to amine radical cation 1(+*) by product radical cation 3(+

226 ional nitrosamine formation when accumulated amines react with residual NOx.

227 When complex mixtures of the amine reactants are employed in competition experiments

228 ctrophiles, which are rapidly intercepted by amine reactants to generate amides/peptides and o-mercap

229 amines are formed under high temperatures by amines reacting with nitrite (a hydrolysis product of NO

230 ines via the Cu(I)-catalyzed aldehyde-alkyne-amine reactions (A(3) coupling) was accomplished.

231 s can be produced more rapidly than carbonyl-amine reactions, therefore providing a satisfactory prot

232 lity and safety as a consequence of carbonyl-amine reactions.

233 oped a robust EV staining strategy, with the amine-reactive fluorescent label, 5-(and-6)-Carboxyfluor

234 We have developed a novel amine-reactive mass defect-based chemical tag, dimethyl

235 n of unactivated alkenes with simple dialkyl amines remains an unsolved problem in organic synthesis.

236 Derivatization of the target amines required minimal sample preparation and resulted

237 rylation of saturated bicyclic and tricyclic amine scaffolds.

238 omide and Me6-TREN (TREN = tris(2-aminoethyl amine)), semi-fluorinated monomers with side chains cont

239 n-Bu2BOTf.i-Bu3N bearing a hindered amine shifts the rate-limiting step to proton transfer.

240 Disruptions of biogenic amine signaling contribute to human neurological disease

241 ral pathways through which parallel biogenic amine signaling tunes behavior appropriately to nutrient

242 Metal-amine solutions provide a unique arena in which to study

243 d from the interaction of CO2 with the solid-amine sorbent, 3-aminopropyl silane (APS), bound to meso

244 We demonstrate that the amine-specific cross-linker Bis(sulfosuccinimidyl)subera

245 observed, including that vertebrate biogenic amines structurally related to octopamine acted as super

246 The effects of amine structure, primarily amine order, on nitrosamine f

247 e at DAT, NET, and SERT, but lengthening the amine substituent from methyl to ethyl, propyl, and buty

248 erivatives of boranephosphonate that contain amine substitutions at boron and the incorporation of th

249 n excited-state iridium photocatalyst and an amine substrate.

250 iodine oxidizes Pd prior to addition of the amine substrate.

251 Only a certain kind of amine (such as HEP) is able to ensure the phase separati

252 oamines results from the production of trace amines (such as tryptamine) by pericytes that ectopicall

253 Biogenic amines, such as like serotonin, are conserved neurotrans

254 series of sterically differentiated tertiary amines suggest that the steric nature of the amine base

255 activating group within a broader context of amine synthesis.

256 inst not only D1-3,5 but also other biogenic amine targets have emerged, and D4 is once again in the

257 ray drying, we show the PSM of two MOFs, the amine-terminated UiO-66-NH2 and the aldehyde-terminated

258 Histamine (HA) is a biogenic amine that can accumulate to high concentration levels i

259 have synthesized 15 new spiroligomer monomer amines that contain two stereocenters and three function

260 AN: N-methyl-N,N-bis[3-(dimethylamino)propyl]amine) that featured an elongated O-O bond but did not l

261 for installation of the t2M motif on primary amines, the method described herein streamlines design o

262 methyl ester derivative with various primary amines, this methodology was used to design a rapid synt

263 thod for direct C-H oxygenation of aliphatic amines through a metal-free activation of molecular oxyg

264 Flowing fluorinated amines through sequential reactor coils mediates diazoal

265 hat develop during the addition of a primary amine to a cyclic sulfate.

266 des was allowing the catalyst, aldehyde, and amine to react for 20 min before addition of the diazo c

267 itions of cyclic and acyclic secondary alkyl amines to a wide range of alkyl olefins with complete an

268 on was also found between the ability of the amines to adsorb on the platinum surface and their perfo

269 oaded, strained C-C and C-N bonds react with amines to allow for the "any-stage" installation of smal

270 anhydride (DA) is used to convert the TAT's amines to carboxylic acid; the resulting DA-TAT is conju

271 l groups can be attached, from Boc-protected amines to fluoroalkanes.

272 on of all acidic sites and the conversion of amines to quaternary ammonium sites.

273 lectrophiles in the presence of nucleophilic amines to yield highly valuable trans-cyclopropylamines

274 We have identified tris(2-aminoethyl)amine (tren)-derived scaffolds with two (t2M) or four (t

275 Only two biogenic amines (tryptamine and tyramine) and two polyamines (spe

276 of aryl donors (Ar-Cl, Ar-Br, Ar-I, Ar-OTf), amine types (primary and secondary), and even alternativ

277 C-2 nucleophilic substitution using several amine types.

278 f the alkene with simple exogenous secondary amines under extraordinarily mild reaction conditions.

279 lective hydrogenation of nitriles to primary amines using a bench-stable cobalt precatalyst under 4 a

280 he alpha-cyanation of secondary and tertiary amines using magnetic nano-ferrites.

281 l cascade for the biocatalytic alkylation of amines using primary and secondary alcohols.

282 (N-[(1-benzyl-1H-indol-3-yl)methyl]pyridin-3-amine, VA012), which exhibited dose-dependent enhancemen

283 At first, the synthesis of propargylic amines via the Cu(I)-catalyzed aldehyde-alkyne-amine rea

284 e demonstrate the direct coupling of CO2 and amines via the single-electron reduction of CO2 for the

285 Additionally, the total amount of these amines was determined by (19)F nuclear magnetic resonanc

286 electivity of azido-Ugi reaction with cyclic amines was investigated.

287 rophenyl)methyl)thio)ethyl)-3-phenylpropan-1-amine) was selected for further development.

288 the chloramination of secondary and tertiary amines, we investigated the kinetics of precursor disapp

289 ontributed to the mutagenicity when aromatic amines were present.

290 The obtained propargylic amines were subsequently transformed to the desired alle

291 lts, derived from alkyl halides and tertiary amines, were the intermediates to yield thioesters.

292 In this study, we hypothesize that aliphatic amines, which are highly abundant among organic micropol

293 ective alpha-C-H coupling of a wide range of amines, which include ethyl amines, azetidines, pyrrolid

294 od depletion nor is it modulated by biogenic amines, which suggest it is not an aversive behaviour.

295 s been ascribed to the presence of secondary amines, which, when oxidized, lose their CO2 capture cap

296 , nitriles, and isocyanides to corresponding amines with excellent activity and selectivity.

297 and, hydroamination generates chiral allylic amines with high regio- and enantioselectivity.

298 unds with a variety of primary and secondary amines with up to >98% conversion and with up to >98% en

299 zed reduction of tertiary amides to tertiary amines, with a useful scope, is demonstrated for the fir

300 om the self-assembly of tris(2-pyridylmethyl)amine zinc complexes through imine condensation chemistr