ライフサイエンスコーパス: aromatization

1 or the last step, forming the pyridine ring (aromatization).

2 via 1,2-alkyl migration and dehydrogenation (aromatization).

3 ldehydes followed by in situ cyclization and aromatization.

4 Spengler cyclization, and a radical-mediated aromatization.

5 ing dipyrromethanes and subsequent oxidative aromatization.

6 ular electrophilic aromatic substitution and aromatization.

7 owed by Lewis acid catalyzed cyclization and aromatization.

8 ding through 1,3-diene formation followed by aromatization.

9 intramolecular Michael reaction, followed by aromatization.

10 on a nitrilium ion intermediate followed by aromatization.

11 ectrocyclization in HMPA followed by in situ aromatization.

12 naphthalene precursors followed by oxidative aromatization.

13 show that Ga Lewis acid sites strongly favor aromatization.

14 ogen secretion versus placental capacity for aromatization.

15 t allylic decarboxylative rearrangement, and aromatization.

16 ainly androgen 19-desmethylation rather than aromatization.

17 enes with 2-methoxybenzoquinones followed by aromatization.

18 hways occur with substrates with no possible aromatization.

19 ver, which has led to accusations of illegal aromatization.

20 3-dipolar cycloaddition, and dehydrogenative aromatization.

21 ed through a 4 + 2 cycloaddition followed by aromatization.

22 polung of imines promoted by organocatalytic aromatization.

23 onalized aromatic ring through deoxygenative aromatization.

24 xide with an enol ether/enamide, followed by aromatization.

25 ed by a mild electrochemical decarboxylative aromatization.

26 ion, aldol condensation, and dehydrogenative aromatization.

27 ndergoes a 1,2-hydrogen shift and subsequent aromatization.

28 s-Alder (ADA) reaction, followed by a facile aromatization.

29 the key acid-promoted heterocyclization, and aromatization.

30 al mediated depropagation reaction driven by aromatization.

31 enes and benzooxanorbornadienes, followed by aromatization.

32 ion to the central allene carbon followed by aromatization.

33 condensation with concomitant debenzylative aromatization.

34 hol components, the dehydrogenations lead to aromatization.

35 Cs, which catalyze C7-C12 cyclization and/or aromatization.

36 ssential to maintain the decarboxylation and aromatization activities and avoid rapid catalyst deacti

37 erein Diels-Alder reactions and a subsequent aromatization afford higher order iptycenes.

38 Subsequent aromatization affords the set of differently functionali

39 n, aldol-type condensation, cyclization, and aromatization, all in the absence of coenzymes or recrui

40 consistent with the above-described partial aromatization and antiaromatization.

41 l rearrangement of a diketo-dioxinone ester, aromatization and cationic diene-epoxide cyclization as

42 ouped into initiation, extension, reduction, aromatization and cyclization, and tailoring steps.

43 Mechanisms for the aromatization and deformylation sequence which are initi

44 This hydration of 5 to 6 leads to aromatization and greatly dominates over water addition

45 cyclohexadienyl radical undergoes concerted aromatization and halogen-atom or group abstraction thro

46 e the carbazole core: 6pi-electrocyclization/aromatization and indole C2-H bond activation/Heck annul

47 uent additive-free thermal treatment induced aromatization and led to exclusively para-connected, hig

48 eventual sacrificial elimination facilitates aromatization and overall benzannulation.

49 nd indole unit to the indolium intermediate; aromatization and oxidation are achieved under air.

50 However, studies on the mechanism of steroid aromatization and subsequent model work have provided ev

51 Biomimetic aromatization and Suzuki-Miyaura cross coupling approach

52 double bond is established under concomitant aromatization and thiophene-ring opening.

53 telomerase expression and activity mainly by aromatization and through ER alpha.

54 2 in breast tumors, as opposed to peripheral aromatization and uptake from plasma, can enhance tissue

55 polymers with varying degrees of chromophore aromatization and used them to probe the effects of synt

56 es a NIS-mediated cascade C-N bond formation/aromatization, and a series of indoles with various func

57 e activities, such as C-C bond desaturation, aromatization, and C-C bond formation, were also observe

58 attenuated astrocyte activation, astrocytic aromatization, and decreased hippocampal E2 levels compa

59 nt onto a furan followed by a fragmentation, aromatization, and N-Boc deprotection cascade.

60 serine mutants gave mixture of dehydrations, aromatizations, and unaltered alcohol side chains depend

61 in, intramolecular C-C bond cyclization, and aromatization as the key intermediates, all occurring in

62 ydrogenated product, which may undergo rapid aromatization, as well as formic acid.

63 e (GVL) over Zn/ZSM-5 to butene, followed by aromatization at high yield with co-feeding of water.

64 corresponding estrogens, a reaction known as aromatization because it involves conversion of the delt

65 cular bisboronate homocoupling and reductive aromatization by H2 SnCl4 .

66 ntramolecular C-N cyclization and subsequent aromatization by the elimination of thiophenol, with goo

67 zed intramolecular Diels-Alder cycloaddition-aromatization cascade constructs the tetrasubstituted ar

68 esults in an unanticipated aza-Michael/aldol/aromatization cascade to give polysubstituted quinolines

69 An electrocyclization-aromatization cascade was utilized to forge the tetracyc

70 ubsequent reductive cyclization/ring-opening aromatization cascade, as was found to occur with the re

71 from the known compound 9, via an unexpected aromatization caused by the addition of PhSeCl and subse

72 hand, the experimental studies revealed that aromatization competes with Michael addition mechanism i

73 Suzuki coupling, followed by dehydrogenative aromatization, completed the synthesis of calothrixin B.

74 Under protic acid-mediated dehydrative aromatization conditions, the central and most strained

75 Dehydrogenative aromatization (DA) of cyclic ketones is central to the d

76 Employing aromatization/de-aromatization metal-ligand cooperation

77 nofunctional, (2) M/NH bifunctional, and (3) aromatization-dearomatization bifunctional molecular cat

78 cer complexes capable of bond activation via aromatization/dearomatization metal-ligand cooperation (

79 e a Lewis base or Lewis acid function, as an aromatization/dearomatization shuttle, or as an electron

80 Estradiol provision via neural aromatization decreases neuro-inflammation and -degenera

81 Driven by aromatization, detosylation of the dihydroquinoline inte

82 position of the allyl fragment enabled by an aromatization-driven Cope rearrangement.

83 oduce 1-hydroxyphenanthrenes through RCM and aromatization-driven keto-enol tautomerism.

84 cy for these initial cycloadducts to undergo aromatization, ene reaction, and oxidation although this

85 , because in this particular case the sum of aromatization energies no longer outweighs the buildup o

86 ), with their energy difference representing aromatization energy (E(aroma)).

87 -1.0 ppm shift corresponds to 24.2 kcal/mol aromatization energy.

88 f central to axial chirality during a double aromatization event triggered by BF(3).OEt(2).

89 on additional driving force associated with aromatization, families of very powerful neutral organic

90 ation and 1,3-functional group isomerization/aromatization followed by terminal oxidation to afford 3

91 Bronsted acid-mediated aromatization, followed by a series of carefully choreog

92 ional role of each domain in cyclization and aromatization for di-domain ARO/CYCs has remained a myst

93 consistent with a nucleophilic addition and aromatization formation mechanism.

94 s constructed via late-stage cyclization and aromatization from a diketodioxinone intermediate and ma

95 tramolecular Friedel-Crafts cyclization, and aromatization furnished the target structures.

96 ol product was investigated and elimination, aromatization, hydrogenation, regioselective O-exchange,

97 ndazol-3-ones underwent unexpected migratory aromatization in acidic condition to produce 3-hydroxy-1

98 cting those in postmenopausal women, in situ aromatization in breast tumor makes a major contribution

99 d females, suggesting a role for presynaptic aromatization in cellular processes within these loci.

100 servation, indicating the lack of peripheral aromatization in OVX mice.

101 ridinium (3-MP) lysine via deoxygenation and aromatization in reagentless conditions.

102 ective effects are mediated, in part, by its aromatization in the dentate gyrus.

103 transfer process dominantly stabilized by an aromatization in the low-energy lying excited state.

104 enhances the selectivity of cyclization and aromatization in the n-hexane reforming reaction.

105 istribution of aromatase suggests a role for aromatization in the regulation of pre- and postsynaptic

106 The novel addition-aromatization inactivation mechanism for 9 contributes t

107 more effective than anastrazole at reducing aromatization-induced ER transactivation and proliferati

108 obese stromal cells exhibited higher maximal aromatization-induced ER transactivation and reduced ana

109 eveal that the crucial step of the oxidative-aromatization involves facile hydride transfer from the

110 ite Pt(1)/CeO(2) toward both cyclization and aromatization is above 86% at 350 degrees C.

111 The new aromatization is also applied to functionalized indoles

112 rresponding cycloadducts, but the subsequent aromatization is complicated.

113 tobase generator (PBG) based on photoinduced aromatization is described.

114 rous dioxygen intermediate mediates androgen aromatization is explored and determined to be unlikely.

115 ion polymerization followed by acid-promoted aromatization is presented.

116 -arylation, and decarboxylation, followed by aromatization, is developed.

117 hich undergoes amination/cascade cyclization/aromatization, leading to N-arylquinazolinium salts in e

118 and 5, a second addition occurs followed by aromatization, leading to the formation of an additional

119 rto elusive methylidyne addition-cyclization-aromatization (MACA) mechanism.

120 Radial aromatization may be a key feature in the repair of the

121 nerability of the CNS we reasoned that brain aromatization may protect circuits from the threats of p

122 In this study, we discover a unique aromatization mechanism involving consecutive [1,2]-alky

123 An elimination-aromatization mechanism is proposed to account for these

124 based inhibitor of BioA that operates via an aromatization mechanism, irreversibly labeling the PLP c

125 thoxy, nitro, etc.) followed by an oxidative aromatization mediated by chloranil.

126 ve and its one-pot two-step ring opening and aromatization mediated by para-toluenesulfonic acid and

127 Employing aromatization/de-aromatization metal-ligand cooperation (MLC) highly enha

128 ions are facilitated by dearomatization, and aromatization metal-ligand cooperation operates in catal

129 een TE and TREN, suggesting that neither the aromatization nor the 5alpha reduction of androgens is r

130 cyclization/[1,5]-H shift/cleavage of CS(2)/aromatization/nucleophilic acyl substitution reaction of

131 cyclization/[1,5]-H shift/cleavage of CS(2)/aromatization/nucleophilic acyl substitution reaction of

132 Aromatization occurs in the medial preoptic area (MPOA),

133 Cyclization and aromatization occurs under the reaction conditions to pr

134 In addition, we have proven that the aromatization occurs via a hydrogen transfer from the cy

135 If the C19 aldehyde remains unhydrated, aromatization occurs with concomitant decarbonylation an

136 bisphenylphosphoryltetrahydroquinolines, the aromatization occurs with elimination of one molecule of

137 An unprecedented DDQ-mediated oxidative aromatization of 2-bezylidene-dihydrofurans yielding 2-a

138 nzyme of AHBA formation, which catalyzes the aromatization of 5-deoxy-5-amino-3-dehydroshikimic acid,

139 iospecific C9-C14 and C7-C16 cyclization and aromatization of a 24-carbon polyketide chain.

140 port a general C-C activation mode driven by aromatization of a pre-aromatic intermediate formed in s

141 Key steps involved polyketide aromatization of a trans, trans-farnesol-derived beta,de

142 tase, or cytochrome P450 19A1, catalyzes the aromatization of androgens to estrogens within the body.

143 lt of enhanced uptake from plasma or in situ aromatization of androgens to estrogens.

144 atase (P450arom), which was confirmed by the aromatization of androstenedione (AD) to E2 and other es

145 d mRNA levels in fat and skin and whole-body aromatization of androstenedione were severely elevated.

146 eactivity patterns, involving stereospecific aromatization of bridges and nucleophile additions.

147 lyzed the cross-dehydrogenative coupling and aromatization of diarylmethyl and dialkyl benzimidazole

148 ng on structure of the starting ketones, the aromatization of intermediate dihydropyrimidines occurs

149 functional groups are obtained by oxidative aromatization of meso-tetraarylporphyrins in which pyrro

150 eforming, the dehydrocyclization and further aromatization of n-hexane are attributed to the prominen

151 al medicines and by the late-stage amination-aromatization of natural products, steroids and terpene

152 oporphyrins (Ar(4)(MeO)(8)TNP) via oxidative aromatization of nonaromatically fused porphyrin precurs

153 2-electron acceptor, catalyzes a remarkable aromatization of piperideine-2-carboxylate (P2C) to pico

154 types of porphyrins were obtained by direct aromatization of precursor porphyrins, annealed with eit

155 crease the degree of carbon condensation and aromatization of SOM functional groups, particularly on

156 erences in response to T are associated with aromatization of T to E and that reduced sensitivity to

157 Aromatization of testosterone (T) to estradiol (E2) duri

158 Our results suggest that aromatization of testosterone into estrogen is important

159 ese increases were considerably greater when aromatization of testosterone to estradiol was also supp

160 Herein, we report alkylative aromatization of tetralone for the synthesis of bioactiv

161 a dienophile component followed by immediate aromatization of the adduct.

162 e intermediate III) followed by an oxidative aromatization of the corresponding Diels-Alder adduct IV

163 henate decarboxylase that avoids the typical aromatization of the cyclohexadienol ring by protonating

164 rgo further dehydration reactions until full aromatization of the cyclohexane ring is achieved.

165 The introduction of H(2) inhibits aromatization of the decomposing polymer and ultimately

166 nium-ion mechanism in light of the fact that aromatization of the dihydro intermediates (formed via a

167 Aromatization of the dihydrofuran rings of these arylalk

168 convergent dibromocyclopropanation and total aromatization of the furobenzocycloalkane are also repor

169 g point instead to electrocyclic closure and aromatization of the heptamethine chain in Cy7 forming F

170 Later, in the presence of DDQ, the aromatization of the indoline derivative was converted t

171 uct the dihydronaphthalene unit of 2 and the aromatization of the intermediate dihydronaphthalene der

172 Aromatization of the latter occurs via beta-C-C bond sci

173 Schiff base to product Schiff base, a facile aromatization of the latter results in a metastable N-ar

174 Dehydration and aromatization of the obtained cycloadducts bearing the r

175 e is followed by cleavage of an O-H bond and aromatization of the PNN ligand to form (PNN)RuH(CO)(OH)

176 [3,3]-sigmatropic rearrangement lead to the aromatization of the product.

177 on with the aryl isocyanates followed by the aromatization of the pyridine/isoquinoline moiety to aff

178 ne intermediate, followed by cyclization and aromatization of the pyrrole ring to give 7.

179 on is stabilized by a combination of partial aromatization of the QM moiety and through-space interac

180 by (optional modification and) base-induced aromatization of the resulting chlorinated oxanorborn(ad

181 pe II dyotropic reaction with concomitant re-aromatization of the six-membered ring.

182 roxylation steps, and the third involves the aromatization of the steroid A-ring, unique to aromatase

183 r controlling specific aldol cyclization and aromatization of these mature polyketide precursors, but

184 Base-promoted debrominative aromatization of these spirocycles unmasked rare and syn

185 : sequential one-pot acylation and oxidative aromatization of vinylogous esters.

186 emonstrate that at high temperatures thermal aromatizations of 2-vinylmethylenecyclopropane (at 700 d

187 provide theoretical insights for the thermal aromatizations of 2-vinylmethylenecyclopropane and 3-vin

188 ing tetrahydrocarbazole and dehydrogenation (aromatization) of this to give the target carbazole (e.g

189 intermediate, which could undergo oxidative aromatization or defluorinative aromatization to form di

190 e, as in the thiopeptide thiostrepton, or an aromatization path to yield the pyridine groups observed

191 way over the more thermodynamically downhill aromatization pathway.

192 nd 1-octen-3-one odorants showed the highest aromatization power.

193 This neural aromatization presumably provides estrogen to steroid-se

194 rrolylbenzenes using a two-step condensation-aromatization procedure.

195 which is rapidly obtained by an oxidative de-aromatization process mediated by a hypervalent iodine r

196 ed by a cyclocarbopalladation/cross-coupling/aromatization process.

197 teristic of 1, by means of an acid-catalyzed aromatization process.

198 ansfer process accompanies the excited-state aromatization, producing a Baird aromatic 8pai core annu

199 structurally closely related to the Bergman-aromatization product of enediyne C-1027.

200 echanistic studies for each step (insertion, aromatization, product release, and nitride regeneration

201 wo different paths, each leading to discrete aromatization products.

202 ort that a branched primary amine bearing an aromatization-prone moiety, ethyl 4-amino-4,5-dihydrothi

203 To overcome this, a dehydrative aromatization protocol using the Burgess reagent was dev

204 -ligand cooperation (MLC) by dearomatization/aromatization provides a unique way for bond activation,

205 These results demonstrate that in situ aromatization rather than uptake can be a determinant of

206 ose that this residue may participate in the aromatization reaction (the third step) by acting as a h

207 Non-oxidative methane dehydro-aromatization reaction can co-produce hydrogen and benze

208 boxylate (P2C) to picolinate in a remarkable aromatization reaction comprising two redox cycles and a

209 essible via acid-mediated Grob fragmentation-aromatization reaction of 1,4,5,6-tetrabromo-7,7-dimetho

210 An unprecedented divergent aromatization reaction of alpha-halobenzyl gamma-butenol

211 n iron(III)-catalyzed cycloisomerization and aromatization reaction produces tetracyclic benzofuran d

212 -mediated one-pot arylation, cyclization and aromatization reaction sequence from 3-acetyl/aroyl-2-pi

213 crucial molecular oxygen-mediated oxidative aromatization reaction sequence in one pot.

214 ne, followed by a cascade of elimination and aromatization reaction sequence to preferentially furnis

215 ddition, and transition metal-free oxidative aromatization reaction sequence utilizing molecular oxyg

216 sized via a facile and mild cyclodehydration-aromatization reaction starting from readily available a

217 NikD catalyzes a remarkable aromatization reaction that converts piperideine 2-carbo

218 nes, and a tandem regioselective Diels-Alder/aromatization reaction.

219 phenylene was demonstrated utilizing a novel aromatization reaction.

220 is predicted to catalyze the final oxidation/aromatization reaction.

221 olo[2,1-a]isoindol-5-one via decarboxylative aromatization reaction.

222 es of Hopf pericyclic reactions, followed by aromatization reactions of the annulated polycyclic arom

223 the amino adduct against further dehydration/aromatization reactions.

224 saturation of the remaining structure, as in aromatization reactions.

225 arbons (PAHs) via gas phase radical mediated aromatization reactions.

226 g exothermic hydrogenolysis with endothermic aromatization renders the overall transformation thermod

227 rmation based on double Michael addition and aromatization (retro-Claisen cleavage and amine eliminat

228 be the development of an iterative reductive aromatization/ring-closing metathesis approach.

229 An intramolecular Diels-Alder reaction-aromatization sequence allows for access to allocolchici

230 talyzed decarboxylative prenyl migration and aromatization sequence as the key step is reported.

231 one-pot C-H alkenylation/electrocyclization/aromatization sequence has been developed for the synthe

232 A regioselective Diels-Alder reaction-aromatization sequence is utilized as the key step in th

233 of K2CO3 in THF ensured a clean deprotection-aromatization sequence to afford the desired heterocycle

234 s-decalin ring, and a 6pi-electrocyclization/aromatization sequence to produce the 2,3-fused carbazol

235 on proceeds through an oxidation/cyclization/aromatization sequence under an atmosphere of O(2) (see

236 ia a one-pot [3+2] cycloaddition/elimination/aromatization sequence-based domino process.

237 ds, which is based on a Diels-Alder reaction-aromatization sequence.

238 ective construction of two new C-C bonds and aromatization sequences under mild and metal-free reacti

239 Both routes avoid the need for a discrete aromatization step and offer significant advantages over

240 A critical tyrosine facilitates the final aromatization step of pyridine formation.

241 Although the last aromatization step proved to be cumbersome, this work un

242 parted by the CF(3) group that disfavors the aromatization step.

243 architectures following cross-couplings and aromatization steps.

244 ormation-[4 + 2] hetero-Diels-Alder reaction-aromatization steps.

245 ational evidence shows that a combination of aromatization, steric and stereoelectronic effects assis

246 Two complementary aromatization strategies involving in situ elimination a

247 A recently developed deoxyfluoroalkylation/aromatization strategy enables conversion of cyclohexan(

248 hesized by application of Grob fragmentation-aromatization strategy to 3-(benzyloxy)-1,4,5,6-tetrabro

249 tate topochemical polymerization/cyclization-aromatization strategy to convert the simple 1,4-bis(3-p

250 ations of the first two rings and subsequent aromatizations take place in the interior pocket.

251 ge stabilization of product arising from the aromatization that accompanies solvent addition to p-qui

252 ation reactions, culminating in an enigmatic aromatization that converts an androgen to an estrogen.

253 cyclopentane carboxylic acids, reluctant to aromatization, the catalytic system facilitates controll

254 Upon subsequent aromatization, the corresponding fully aromatic function

255 n or reaction with a Grignard reagent before aromatization; the latter process gives compounds in whi

256 ) as a base in DMF at 110 C with concomitant aromatization through an elimination of tosylsulfinic ac

257 bstrates not blocked by geminal substitution aromatization to a dipyrromethane is a competing side re

258 action with a carbon nucleophile followed by aromatization to afford alpha-methylated pyrazines and p

259 t room temperature then results in efficient aromatization to benzene derivatives of a regiochemicall

260 ns in regulating HPA activity may be through aromatization to estradiol, or by 5alpha-reduction to th

261 en receptor-mediated mechanisms or via local aromatization to estradiol.

262 d antidepressant effects, likely mediated by aromatization to estrogen metabolites, in the sucrose pr

263 obably involves a transamination followed by aromatization to form an aromatic thiophene ring.

264 go oxidative aromatization or defluorinative aromatization to form different carbon-atom insertion pr

265 [4 + 2] cycloaddition loss of a nitrile and aromatization to generate a 1,2,4-triazine derivative.

266 (II)-C palladacycle followed by an oxidative aromatization to generate the pyridine core.

267 in then mediates elimination of pyruvate and aromatization to give PABA.

268 by intramolecular cyclization and subsequent aromatization to give the annulated products.

269 ade alkylation, formylation, annulation, and aromatization to make substituted biaryls.

270 followed by spontaneous proton loss with re-aromatization to provide the tetrahydroisoquinoline prod

271 rature results in smooth loss of bromide and aromatization to resorcinol monomethyl ethers of defined

272 Further aromatization to the corresponding xanthones is readily

273 Cyclization of the monosulfide with aromatization to the thiophene product is the only drivi

274 hloride to the reaction mixture, a selective aromatization to yield the corresponding pyrroles substi

275 hoxy- and ethoxy carbonyl shift, and finally aromatization to yield the desired product.

276 thesis reaction, followed by elimination and aromatization, to furnish a key pentasubstituted pyridin

277 ryl bromides and oxanorbornenes, followed by aromatization under acidic conditions.

278 ergo bent-to-planar transformation driven by aromatization under electrochemical control.

279 ethane derivatives by 1,6-conjugate addition/aromatization under mild reaction conditions without any

280 clohex-1-ene-4,5-diols, which are subject to aromatization upon dehydration or Nicholas diol deoxydeh

281 g openings of 2H-azirine followed by in situ aromatization using a catalytic amount of Bronsted acid

282 Subsequent aromatization using cesium carbonate gave rise to isopro

283 s five fast radical cyclizations followed by aromatization via a 1,5-H shift with a >93% yield per st

284 th hydrogen, alcohols, or nitriles to regain aromatization via MLC.

285 n to yield the formal "6-endo" products with aromatization via stereoelectronically assisted C-C bond

286 lly in all testosterone-dose groups in which aromatization was also suppressed, and this decline was

287 conditions and palladium-catalyzed oxidative aromatization was developed for the synthesis of hexahyd

288 model, the confounding effect of peripheral aromatization was first excluded experimentally.

289 ring size on the reaction rate of oxidative aromatization was investigated.

290 Decreases in DXA BMD were observed when aromatization was suppressed but were modest in most gro

291 f experiments examining injury-induced glial aromatization, we identified aromatase in radial glia of

292 The biological effects of in situ aromatization were then directly examined.

293 Another option is methane aromatization, which produces benzene and hydrogen: 6CH4

294 recursors followed by 6pi-electrocyclization/aromatization, while isomeric TD-syn-TBDT and TD-anti-TB

295 adducts with Fe2(CO)9 followed by oxidative aromatization with 2,3-dichloro-5,6-dicyano-1,4-benzoqui

296 lic addition to the aldehyde and dehydrative aromatization with concomitant loss of formic acid led t

297 lly and then subjected to thermally promoted aromatization with elimination of sulfur(IV) oxide and a

298 ed perylene derivatives by deoxygenation and aromatization with HCl/EtOH.

299 equential Diels-Alder reaction and oxidative aromatization with the preformed glycosyl diene and dien

300 Finally, the contribution of testosterone's aromatization within the dentate gyrus was assessed by l