ライフサイエンスコーパス: in high yield

1 versity of new thioether (hetera)cyclophanes in high yield.

2 eCN at room temperature produced imidazoline in high yield.

3 nsfer to provide the corresponding fluorides in high yield.

4 to a cycloparaphenyleneacetylene derivative in high yield.

5 yrosine peptides into sulfotyrosine peptides in high yield.

6 tic process and to obtain the target protein in high yield.

7 tion the corresponding adducts were obtained in high yield.

8 nous acetylation at multiple lysine residues in high yield.

9 lizidines were obtained diastereoselectively in high yield.

10 at allow isolation of an enantiopure product in high yield.

11 er, and i-Pr2NEt gives 2,5-diaryl-1,5-dienes in high yield.

12 onjugated to carbonyl groups are synthesized in high yield.

13 n of a lanthanide-functionalized [2]rotaxane in high yield.

14 carbon centers can be synthesized easily and in high yield.

15 eryl alpha-d-galactopyranoside were prepared in high yield.

16 degradation and is challenging to synthesize in high yield.

17 y preparing a variety of alpha-aryl glycines in high yield.

18 yields 3-methyl-1-phenyl-2-azabutadiene (18) in high yield.

19 expressed UCP1 in Escherichia coli membranes in high yield.

20 nane ether intermediates at room temperature in high yield.

21 ety of telechelic functionalized polyolefins in high yield.

22 1 with high regio- and diastereoselectivity in high yield.

23 m the A/B/C/D rings of (+/-)-minfiensine (2) in high yield.

24 omplex [Cu2(mu-eta(1):eta(1)-Ph)DPFN](NTf2)2 in high yield.

25 erize alkynes to form conjugated macrocycles in high yield.

26 on in the nucleoside's excited triplet state in high yield.

27 stereocontrol, leading to beta-amino ketones in high yields.

28 es and 4-(1H-pyrrol-3-yl)-1H-1,2,4-triazoles in high yields.

29 tarting from 3-amino-2H-chromen-2-one, again in high yields.

30 onded phenolates hydroxylate to catecholates in high yields.

31 ing fused pyrrolecarboxylic acid derivatives in high yields.

32 wed by air oxidation to furnish the products in high yields.

33 a variety of aliphatic [(18)F]CF3S compounds in high yields.

34 alkenyl or N-(o-thio)aryl group was obtained in high yields.

35 rnishing the fused indolo[2,1-a]phthalazines in high yields.

36 synthesised via Oxa-Pictet-Spengler reaction in high yields.

37 lene (1) and 1-bromo-5-methylnaphthalene (2) in high yields.

38 ently converted into oximes using SnCl2.2H2O in high yields.

39 3-cyanobenzo[b]- and/hetero-fused thiophenes in high yields.

40 readily available, and products are obtained in high yields.

41 aryl halide to give tetrasubstituted alkenes in high yields.

42 broad functionalities have been synthesized in high yields.

43 o cysteine residues and an alpha,omega-diene in high yields.

44 ntroduced that affords aryl alkyl sulfoxides in high yields.

45 olation of novel functionalized diphosphines in high yields.

46 rd alpha-aryl-alpha,alpha-difluoroacetamides in high yields.

47 n of disubstituted alkynes affords Z-alkenes in high yields.

48 ion of primary amides, carbonates, and ureas in high yields.

49 hyl radical formation and finally to methane in high yields.

50 o furnish a library of 1,3-diynes and enynes in high yields.

51 methylarenes, and difluoromethylheteroarenes in high yields.

52 ld and fast method to stannylate azobenzenes in high yields.

53 Tf, SPh), cleanly affords (R3 SiO)2 UX2 (L)2 in high yields.

54 aryl substituents, were successfully reacted in high yields.

55 ent, ene reaction, and O-alkylation occurred in high yields.

56 access a variety of imides as well as amides in high yields.

57 nt Lys, Cys, and Tyr residues in thioredoxin in high yields.

58 ysis to form the corresponding NH tetrazoles in high yields.

59 s to produce C(sp(2))-H alkoxylated products in high yields.

60 and C-C bonds and gives unique metallacycles in high yields.

61 ve highly substituted 4-nitro-4-isoxazolines in high yields.

62 -containing hypervalent iodine(III) reagents in high yields.

63 acetonitrile underwent reductive elimination in high yields.

64 or 3-bromobipyridine N-oxides were obtained in high yields.

65 uence furnishes quadruply annulated borepins in high yields.

66 f C(sp(3))-S and C(sp(3))-N coupled products in high yields.

67 odides to provide the meta-arylated products in high yields.

68 and 0D (C4 N2 H14 Br)4 SnBr6 can be prepared in high yields.

69 e of Yb(OTf)3 to afford the desired products in high yields.

70 )-1H-1,2,4-triazole-5(4H)-thiones are formed in high yields.

71 a-Baylis-Hillman alcohols to give 1,4-dienes in high yields.

72 erocycles and oxoaldehydes under ambient air in high yields.

73 PEG-based crosslinker, which are synthesized in high yields.

74 extended to produce other layered materials in high yields.

75 lalanine (2e), glycine (2f) and leucine (2g) in high yields (43-82%).

76 der CO(g) to afford the dicarbonyl complexes in high yield (50-90%).

77 ribose, which produces TAP-ribose conjugates in high yield (60-90%).

78 trans-1-trifluoromethyl-2-arylcyclopropanes in high yields (61-99%) and excellent diastereo- and ena

79 tituted bicyclo[4.2.2]deca-2,4,7,9-tetraenes in high yields (68-85%).

80 -1-yl]-5H-1,2,3-dithiazol-5-ylidene}anilines in high yields (70-92%).

81 toward this distinctive polymer architecture in high yield ( 75%) via efficient ring closing of ratio

82 ctively the asymmetrically substituted ester in high yields (80-100%).

83 providing the corresponding 4-oxopiperidines in high yields (80-89%).

84 c anhydrides of varying alkyl chain lengths, in high yields (80-95%).

85 hydroxy-1,3-diaminoprop ane) was synthesised in high yield (90 %).

86 parum, which fermented glycerol into ethanol in high yields (90%) and produced fermentative byproduct

87 nes to afford the corresponding cycloadducts in high yields (90-98%).

88 zed by chiral squaramides and afford adducts in high yields (90-99%) and with excellent enantioselect

89 ransposed were synthesized regiospecifically in high yields (94 and 92%, respectively) by the Wang-Pe

90 ynthesize these ultrathin (2 nm wide) Au NWs in high yield (95%) by reducing HAuCl4 in the presence o

91 a) 3 (same conditions) gave NDA cycloadducts in high yields (97-99%) with no ene product from 2,3-dim

92 three distinct groups of aromatic compounds in high yields acetals, ethanol and ethyl aromatics, and

93 raldehyde to give a 12:1 syn:syn selectivity in high yield along with small amounts of one anti isome

94 N2O were recovered from the reaction mixture in high yields, along with N,N'-dibutylbenzamidine.

95 (18)F-AMBF3-TATE was radiolabeled in high yield and at high specific activity, did not req

96 s from N-Boc-L-tyrosine on a multigram scale in high yield and attached to Merrifield-Cl resin via it

97 urification procedures that afford materials in high yield and avoid chromatographic purification.

98 We found that the anti adduct was obtained in high yield and diastereoselection as was demonstrated

99 a variety of cis-2,3-disubstituted indolines in high yield and enantioeselectivity.

100 ted to form substituted dehydropiperidinones in high yield and enantiomeric excess.

101 The reaction proceeds in high yield and enantiospecificity for benzylic ethers

102 ination to generate terminal alkyne products in high yield and excellent levels of enantiospecificity

103 he synthesis of substituted D-phenylalanines in high yield and excellent optical purity, starting fro

104 aternary protected 2-amino-2-vinyl-1,3-diols in high yield and excellent stereochemical purity.

105 SbO4L was synthesized in three simple steps in high yield and found to be a highly selective, direct

106 (89)Zr-labeling of Df-ALT-836 was achieved in high yield and good specific activity.

107 oupling reaction generally provides products in high yield and high selectivity (>95:5 enantiomer rat

108 The ability to prepare these TMD nanosheets in high yield and large scale via various methods has le

109 an all-carbon-atom quaternary stereocenter, in high yield and optical purity.

110 zed into corresponding mononitro derivatives in high yield and purity without employing any protectio

111 eloped for the isolation of (223,224,225)Ra, in high yield and purity, from a proton irradiated (232)

112 -benzylpyrrole has made the alkene available in high yield and purity.

113 e range of functional groups can be oxidized in high yield and regioselectivity.

114 rized radical addition to aromatic compounds in high yield and selectivity.

115 re performed on the chiral benzylic alcohols in high yield and stereoselectivity.

116 arbene=:C[(Pr(i) )NC(Me)]2 ) was synthesized in high yield and structurally characterized.

117 2].32H2O (Na6K4-Ni4P2), has been synthesized in high yield and systematically characterized.

118 n-poor, and sterically hindered aryl iodides in high yield and tolerates a variety of functional grou

119 tetracyclic tetralin analogues were prepared in high yield and up to 20/1 diasteroselectivity from cy

120 etic resolution afforded the target compound in high yield and up to 99% ee.

121 variety of functional groups are transformed in high yield and very high regioselectivity.

122 (18)F-SO3F(-) is easily synthesized in high yield and very high specific activity and is a p

123 imelteon, Ticagrelor, and a TRPV1 inhibitor) in high yield and with excellent diastereo- and enantios

124 c shift to afford the boronic ester products in high yield and with excellent enantiospecificity.

125 ylations of N-Boc alpha-amino acids, proceed in high yield and with excellent olefin geometry control

126 reaction affords terminal E-alkenyl bromides in high yield and with excellent regio- and diastereosel

127 y disfavored alkenyl chlorides and fluorides in high yield and with exceptional stereoselectivity.

128 avity and portal are difficult to synthesize in high yield and with good structural fidelity.

129 e method produces all major species of ncRNA in high yield and with high integrity, enabling direct c

130 n forms 1-cyclopropyl alkylamine derivatives in high yield and with high regio- and diastereoselectiv

131 Products are formed in high yield and with high regioselectivity.

132 olabeled in a 1-step (18)F exchange reaction in high yield and with high specific activity.

133 ing di- or trisubstituted alkenes, typically in high yield and with high stereoselectivity.

134 FVT of the azide produces the nitrene in high yield and with only minor contaminations of the

135 d degree of symmetry control can be obtained in high yield and with remarkable monodispersity.

136 to convert propargylic alcohols to 1,3-diols in high yield and with retention of stereochemistry at t

137 of lactones with sodium trimethylsilanolate in high yields and aprotic solvents is described.

138 he reaction products were generally obtained in high yields and as a single diastereoisomer having th

139 itrothioesters with quaternary stereocenters in high yields and diastereo- and enantioselectivities.

140 ation of 1,2,3-substituted borocyclopropanes in high yields and diastereoselectivities.

141 diaryl and triaryl quaternary stereocenters in high yields and ee's.

142 lution, furnishing both epoxide and thiirane in high yields and enantiomeric purity.

143 at reactions of alpha-fluorotetralones occur in high yields and enantioselectivities when conducted w

144 performed and yields versatile intermediates in high yields and enantioselectivities.

145 ta-lactones are formed under mild conditions in high yields and enantioselectivities.

146 In both cases, the products are obtained in high yields and enantioselectivities.

147 and western fragments was set catalytically in high yields and excellent de by a zinc-ProPhenol-cata

148 on (DKR) to convert primary amines to amides in high yields and excellent ee's.

149 with a N-containing quaternary stereocenter in high yields and excellent enantioselectivities.

150 uced the corresponding cyclic indole aminals in high yields and excellent enantioselectivities.

151 ide range of alkynes furnishing the products in high yields and excellent enantioselectivity.

152 yl-1,1,3,3-tetracyanopropenides (ATCN) salts in high yields and excellent purities starting from read

153 es to produce valuable diarylalkane products in high yields and excellent regioselectivity.

154 s to alpha-indole-gamma-substituted lactones in high yields and good diastereoisomeric and enantiomer

155 e corresponding aldol products were obtained in high yields and good to excellent diastereoselectivit

156 rded pyrrolidines, piperidines, and azepanes in high yields and high enantiomeric ratios via enantios

157 elivering the chiral barbiturate derivatives in high yields and high enantioselectivities, even with

158 tes activates this transformation to proceed in high yields and in a regio- and diastereoselective ma

159 stituted polycyclic dibenzofuran derivatives in high yields and in an atom-efficient and environmenta

160 o generate the desired gamma-crotonolactones in high yields and levels of enantioselectivity.

161 ]fluoroethyl-phenethyl-orvinol were prepared in high yields and quality from their 6-O-desmethyl-prec

162 etrasubstituted stereocenter can be isolated in high yields and selectivities for further derivatizat

163 igand and K2CO3 as the base, and gave amides in high yields and selectivities using 1,3-bis(diisobuty

164 3- or 4-Aminophenols afforded esters in high yields and selectivities using 1,3-bis(diphenylp

165 nitrile, while branched amides were obtained in high yields and selectivity in butanone by changing t

166 s the additives, linear amides were obtained in high yields and selectivity using tris(4-methoxypheny

167 ficient preparation of the arylated products in high yields and short residence times.

168 th a chiral N-mesyloxycarbamate was achieved in high yields and stereoselectivities using Rh2[(S)-ntt

169 the formation of [Cp''2Zr(eta(1:1)-As4)] (1) in high yields and the arsenic-rich complex [(Cp''2Zr)(C

170 g stable precursors of alpha-hydrazinoimines in high yields and with almost complete enantioselectivi

171 ting vicinal chirality centers were obtained in high yields and with excellent enantio-, diastereo-,

172 carbo- and heterocyclic five-membered rings in high yields and with good to excellent diastereo- and

173 olecular silylation of cyclopropyl C-H bonds in high yields and with high enantiomeric excesses in th

174 ,4-dipoles to give polysubstituted tetralins in high yields and with high regio- and diastereoselecti

175 ins to generate branched vinylfuran products in high yields and with high selectivities with a second

176 be the preparation of cellulose nanocrystals in high yields and with minimal water consumption.

177 l phosphine, 3,4-dihydropyrans were obtained in high yields and with virtually perfect enantioselecti

178 ariety of pi-extended triptycenes accessible in high yields and without the necessity of column chrom

179 The reactions proceed in high yield, and functional groups such as halides, si

180 thorium and uranium complexes were obtained in high yields, and their structures were established by

181 and the conditions to obtain single crystals in high yield are detailed.

182 eveloped to afford chromanone-3-carboxylates in high yields as a single diastereomer.

183 by polymer chemists to post-modify polymers in high yields, as well as to effectively catalyze rever

184 gonucleotides to install a single cross-link in high yield at a specified location within a DNA duple

185 aliphatic and aromatic alkynes are hydrated in high yield at ambient temperature.

186 hiometric oxidant, and the reactions proceed in high yield at Pt loadings as low as 1 mol%.

187 broad scope of aryl iodides can be prepared in high yields at room temperature under exceptionally m

188 ins can now be stereospecifally transformed, in high yields at room temperature, into valuable NH azi

189 ng product [(Cp*Ir(NHC)Cl)2][(BAr(F)4)2], 4, in high yields at the end of the reaction suggests that

190 cted alkenes are formed with E configuration in high yields, but when exposed to nitroalkanes under b

191 target compounds were in most cases obtained in high yields, but with moderate enantiomeric ratios (u

192 erto unreported products are easily isolated in high yield by a simple filtration step.

193 an analysis relies on their chemical release in high yield by hydrazinolysis, followed by fluorescent

194 e easily prepared with good size control and in high yield by reacting the metal precursors (copper i

195 polymers with benzothiadiazole were prepared in high yield by Suzuki polymerization to afford materia

196 )Ga(H)[Fe(CO)4] (9) can be obtained directly in high yield by the reaction of the (bisNHC)Ga(Cl)[Fe(C

197 thesis of eudistidine C (1) was accomplished in high yield by treating eudistidine A (2) with 4(2-ami

198 ereoselective manner to give vinylaziridines in high yields by means of the metal-mediated transfer o

199 as employed to synthesize conjugated BODIPYs in high yields by treating formylated BODIPYs with alkyl

200 caused by increasing temperatures is higher in high-yielding environments (e.g., northern India) bec

201 Photoproduction of N2O occurs in high yield for 1a but not 2a.

202 The two key building blocks can be prepared in high yield from commercially available starting mater

203 on of phosphorylated diamantane was achieved in high yield from the corresponding phosphonates.

204 Yet it can be formed in high yield from, for example, benzyl alcohol by oxida

205 mino/hydroxythiophenes were readily obtained in high yields from easily accessible precursors, in a s

206 The target products are synthesized in high yields from guanidylpyridines and analogues via

207 -group tolerance, and products were isolated in high yields, generally without the requirement for pu

208 a one-step process by the nitration of FOX-7 in high yield (>93%).

209 chain transfer agent (macro-CTA) is prepared in high yield (>95%) with 97% dithiobenzoate chain-end f

210 photochemical deprotection was accomplished in high yields (>80%).

211 ep was completed in a short time (1-2 h) and in high yields (>90%), due to the intrinsic rigid struct

212 ingle leftover phenolic moiety were isolated in high yields (>90%).

213 product from a benzylic trichloroacetimidate in high yield have been developed.

214 erved in the tandem reaction, which proceeds in high yield in 1-3 h.

215 e used in one pot and products were obtained in high yield in an easy workup procedure.

216 [(99m)Tc(PS)2(Ln)] complexes were prepared in high yield in nearly physiologic conditions following

217 Cl2 with TPPO precipitates a TPPO-Zn complex in high yield in several common polar organic solvents.

218 n cross-coupling to form C-N bonds, occurred in high yield in the presence of a catalyst derived from

219 used pyridoindolone derivatives are obtained in high yields in a relatively short period of time unde

220 allows direct access to cyclic vinyl ethers in high yields in a single step.

221 azepines were obtained from these precursors in high yields in an alkylation/annulation sequence.

222 nchona alkaloid-derived dimers were obtained in high yields in copper-catalyzed 1,3-dipolar "click" c

223 the direct ortho-alkylation can be achieved in high yields in the presence of an iron source, 1,2-bi

224 of oxetane 2,2-dicarboxylates were accessed in high yields, including functionalized 3-/4-aryl- and

225 ent organic framework (COF) nanosheets (NSs) in high yield is of great importance for the further exp

226 sults identify dG oxidation to d2Ih to occur in high yields leading to a hypothesis that d2Ih could b

227 The synthesis is achieved in high yields making use of an intramolecular direct ar

228 Recent progress in high-yield, massive production of ultrathin 2D nanoma

229 ting of a CGA moiety, caffeic acid, resulted in high yield of CO2 (>98%), suggesting that CGA hydroly

230 ults indicate that CO2 enrichment can result in high yields of red leaf lettuce rich in phenolic comp

231 d to label ATP and GTP site specifically and in high yields of up to 90%.

232 bstituted 1-naphthalenones could be prepared in high yields of up to 91%.

233 oupling reaction generally provides products in high yields, offers an expansive substrate scope, and

234 ionally reactive and are able to participate in high-yielding olefin metathesis reactions that afford

235 ed by oxidation to give the desired products in high yield on scales of up to 25 g.

236 ed by a cofacial porphyrin scaffold accessed in high yield (overall 53%) using coordination-driven se

237 ccessfully prepared with good uniformity and in high yield, Pd right bipyramids (RBPs) that have a si

238 The cross-coupling products were obtained in high yields ranging from 70 to 93%.

239 oad range of functional groups were obtained in high yields, regioselectivities, and diastereoselecti

240 s [(bisNHC)AlBr2](+)Br(-) (2) as an ion pair in high yield, representing the first example of a bisNH

241 tuted quinazolin-4(3H)-ones were synthesized in high yields starting from readily available benzyl al

242 d into 2-(9'-fluorenylmethyloxy)-2-oxazoline in high yield, thereby providing a new pathway for the s

243 nyl-1,3-diazabicyclo[3.1.0]hexane structures in high yields through intramolecular radical aziridinat

244 acid derivatives were subsequently converted in high yields to enantiopure beta-functionalized cystei

245 ubstrates were found to be rapidly converted in high yields to their corresponding alpha-tosyloxy ket

246 or redox oxide catalysts to produce methanol in high yields, together with other useful chemicals, in

247 and lipid biosyntheses can be reconstituted in high yield under mild, prebiotically plausible condit

248 oxidation of benzylic alcohols to aldehydes in high yield under purely aqueous conditions, at room t

249 id synthesis of 1,3-substituted cyclobutanes in high yield under simple and robust reaction condition

250 2-Aminophenol only gave amides in high yields under both conditions.

251 roxyiminoimines to trisubstituted imidazoles in high yields under mild conditions.

252 ach delivers the desired molecular scaffolds in high yields (up to 82%) with excellent stereoselectiv

253 ed to afford fused bicyclic dihydropyridines in high yields (up to 94%) with high enantioselectivity

254 diastereoselectivities (up to 98:2 d.r.) and in high yields (up to 96 %).

255 3,3,3-trifluoropropanes [Ar(Ar')CH-CH(X)CF3] in high yields (up to 96%) as a mixture of two diastereo

256 ering fully substituted unsymmetrical amides in high yields (up to 96%).

257 one products with excellent regioselectivity in high yields (up to 96%).

258 ilylesters and alpha-thioesters was obtained in high yields (up to 98%) from alpha-diazoesters using

259 ature to give a series of homoallylic amines in high yields (up to quant) and diastereoselectivity (u

260 sizes and heteroatoms have been synthesized in high yield using this mild acid-catalyzed reaction.

261 dment of (100)Mo can be practically achieved in high yields using conventional medical cyclotrons.

262 iazine derivatives were selectively prepared in high yields using microwave irradiation.

263 the recovery of the enantiopure (S)-alcohols in high yields using the alcohol dehydrogenase from Rhod

264 olyl glycoconjugates 6a-u have been achieved in high yields via 1,3-dipolar cycloaddition of compound

265 2-c]quinazoline-6-carbonitriles are prepared in high yields via three new routes: (1) a Cu(OTf)2 (0-5

266 tonate) have been obtained on a large scale, in high yield, via one-pot reaction that utilizes commer

267 at microcompartment shells could be purified in high yield when all seven H. ochraceum BMC shell gene

268 of unprecedented [3]naphthylene regioisomers in high yields, where three naphthalenoids are fused thr

269 of imines and enals, and can be carried out in high yield with as little as 0.01 mole per cent catal

270 The reaction proceeds in high yield with as little as 1000 ppm catalyst loadin

271 f alpha-diazo dihydroindolinone 21 proceeded in high yield with excellent diastereoselectivity to giv

272 ous quaternary carbons in a single operation in high yield with excellent diastereoselectivity.

273 erivatives undergo asymmetric C-H silylation in high yield with excellent enantioselectivity in the p

274 active secondary alcohols could be obtained in high yield with good to excellent enatioselectivities

275 lting chiral products are typically obtained in high yield with good to excellent levels of enantiose

276 methanes and other 1,1-diarylalkane products in high yield with good to high regioselectivity.

277 ve alkaloid-inspired tetrahydroindolizidines in high yield with high diastereoselectivity.

278 ay of potassium (hetero)aryltrifluoroborates in high yield with low catalyst loadings under mild reac

279 mates with electrophilic metalloenolcarbenes in high yield with up to 98 % ee and excellent diastereo

280 uble C-O coupling products chemo-selectively in high yields with a broad substrate scope.

281 These reactions proceed smoothly and in high yields with both enolizable and non-enolizable s

282 The desired methyl ketones were obtained in high yields with complete regioselectivities.

283 C bond formations with imines have proceeded in high yields with complete regioselectivity and excell

284 synthesis of substituted cyclic sulfoximines in high yields with complete stereocontrol, and tolerate

285 nditions, the desired products are delivered in high yields with ee values of up to 98 %.

286 s, affording the corresponding cyclopropanes in high yields with effective control of both diastereo-

287 d acetals, ketals, or aminals have proceeded in high yields with essentially complete regio- and chem

288 benzaldehydes and aromatic ketones generally in high yields with excellent chemoselectivity and very

289 The reactions form dihydrobenzosiloles in high yields with excellent enantioselectivities by fu

290 d cis-3,6-disubstituted dihydro-1,2-oxazines in high yields with excellent regio-, diastereo-, and en

291 affords syn beta-hydroxy-alpha-amino esters in high yields with good to excellent levels of diastere

292 quaternary stereogenic centers were isolated in high yields with high to excellent enantioselectivity

293 the preparation of the poly(propylene oxide) in high yields with high turnover (TON>2000), which rend

294 flate, Mannich addition products were formed in high yields with near exclusivity under otherwise ide

295 method to prepare crystals of a novel shape in high yield, with good homogeneity, and with excellent

296 d by boron trifluoride results in cyclic PPA in high yield, with high molecular weight, and with extr

297 The cycloadditions proceeded in high yields, with the cyclophane reacting faster than

298 and successive functional group conversions in high yields without any racemization of the stereogen

299 gives water-soluble altrose PASs (alt-PASs) in high yields without degradation of the polymer backbo

300 ated carbon and furnishes arenes and phenols in high yields without hydrogenation.