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1  1,5-diazahexa-1,3,5-triene, followed by 1,6-cyclization.
2  directed remote metalation (DReM)-initiated cyclization.
3  is faster than the respective 5-exo radical cyclization.
4 e of the triazole ring followed by oxidative cyclization.
5 e primary product of 1,4-diazahexatriene 1,5-cyclization.
6 n allied to an iridium-catalyzed dehydrative cyclization.
7 adening the scope of this asymmetric Nazarov cyclization.
8 non-like modes play an important role in DNA cyclization.
9 )-pyridines via acid promoted intramolecular cyclization.
10 tion, and THP formation via Pd(II)-catalyzed cyclization.
11 on and supporting rate-determining concerted cyclization.
12 lamino-ynol derivatives via a gold-catalyzed cyclization.
13 mino ynone generation followed by 6-endo-dig cyclization.
14 cid, via intramolectular [2+2]-photochemical cyclization.
15 reviously proposed mechanism of PT-catalyzed cyclization.
16 efin isomerization, 1,2-addition followed by cyclization.
17 rminal alkenes and intramolecular aza-Wacker cyclization.
18 n, oxo-vanadium oxidation, and atom-transfer cyclization.
19  alkylation and a diastereoselective pinacol cyclization.
20 lowed by Lewis acid catalyzed intramolecular cyclization.
21 es were employed to examine the scope of the cyclization.
22 ive moieties, particularly polyenes prone to cyclization.
23 tandem [3,3]-sigmatropic rearrangement-[2+2]-cyclization.
24  which undergoes an interrupted halo-Nazarov cyclization.
25 shed via condensation and two intramolecular cyclizations.
26                 Through a tandem guanylation-cyclization, a series of 2-iminoimidazolin-4-ones could
27 e carbamate formation, lactone reduction and cyclization, afforded cyclopropyl pyran 1.
28                                              Cyclization also folds peptides into bioactive conformat
29 xa-2,4-dienones with ethyl acrylate, radical cyclization and 1,3-acyl shift in excited state are the
30  acid (chiral LBA) mediated cationic polyene cyclization and a titanocene-mediated radical cyclizatio
31 oxycyclopropyl)but-2-enoate (28) followed by cyclization and chiral separation to form 27c, the core
32 zed Ser65-Tyr66-Gly67 tripeptide, we modeled cyclization and dehydration reactions.
33 further probes the dimer-driven mechanism of cyclization and enables an efficient access to a wide ra
34  have been demonstrated to increase rates of cyclization and impose stereochemical constraints on the
35 ving alkynes and readily mediates both enyne cyclization and intramolecular hydroarylation reactions,
36  of which are productive for bi- (or larger) cyclization and lead to products.
37 dyl radicals and their use in hydroamination-cyclization and N-arylation reactions is reported.
38  Ugi post-transformation involving catalytic cyclization and oxidative Heck reaction sequence.
39 re shown to be superior reagents for protein cyclization and protein semisynthesis, with the latter i
40 lude pericyclic, cycloaromatization, radical cyclization and ring opening, and SN 2.
41 or lipoxin B4, likely by interfering with AA cyclization and shunting AA to the LOX pathway under phy
42 uggesting cationic charge buildup during the cyclization and supporting rate-determining concerted cy
43  occurs alongside, or instead of, borylative cyclization and the factors controlling the reaction out
44  The epimerized hexaketide failed to undergo cyclization and was exclusively hydrolyzed, confirming t
45  that enantioselective SmI2-mediated radical cyclizations and cascades that exploit a simple, recycla
46       Highly selective dearomatizing radical cyclizations and cyclization cascades, triggered by sing
47  non-ribosomal peptide ferribactin undergoes cyclizations and oxidations that result in the fluoropho
48 e stabilization of alkenyl anions in anionic cyclization) and nanomaterials chemistry (facile doping
49 ylofuranose precursor, [I(+)]-induced 6-endo cyclization, and 1,2-trans stereoselective glycosylation
50 mination of the photoredox-catalyzed radical cyclization, and a double 6-endo cyclization with cataly
51 on of methyllithium to the nitrile function, cyclization, and in situ acylation with di-tert-butyldic
52 rmation involves consecutive transamination, cyclization, and isomerization steps.
53  steps of amidation, alcohol activation, and cyclization are all mediated by one reagent (TBD) in a s
54 a C6F5-substituted formazan undergoes facile cyclization as a result of intermolecular nucleophilic s
55                        Here we used backbone cyclization as a strategy to improve the folding yield a
56    The reaction provided an unusual mode for cyclization as sodium sulfide, a soft nucleophile, prefe
57 iethynylquinoxaline showed C(1)-C(6) Bergman cyclization as the favored thermodynamic reaction pathwa
58   A plausible mechanism is proposed for this cyclization based on the results of a control experiment
59  these reactions, exemplified by the Bergman cyclization (BC), two bonds are sacrificed to form a sin
60               However, competitive 5-exo-dig cyclization, beta-elimination of the ynone, and dimeriza
61  catalysis of rhodium(II) octanoate, [3 + 2]-cyclization between enoldiazoacetamides and nitrosoarene
62 een developed by employing Michael-Dieckmann cyclization between enone 3 and a fully built and protec
63 a one-pot sequential N-acylation/dehydrative cyclization between ethyl carbazate and N-acylbenzotriaz
64 e (B(C6F5)3), an activating agent capable of cyclization but not dealkylation, resulted in the isolat
65 oach to azetidine synthesis than traditional cyclization by nucleophilic displacement and provide nov
66 rug cleavage unless 3-exo-tet intramolecular cyclization can occur, suggesting that enzymatic hydroly
67 s a novel intermolecular [4+2] cycloaddition-cyclization cascade between a vinyl p-quinone methide an
68 face-catalysed cross-coupling and sequential cyclization cascade of 1,2-bis(2-ethynyl phenyl)ethyne o
69 te a highly stereoselective C-C bond-forming cyclization cascade reaction using (2-halo)aryl ethers a
70 precedented NaBH4-promoted one-pot reductive cyclization cascade that efficiently yielded a hydroxyl
71 ein engineering can be used to reprogram the cyclization cascade to generate alternative and commerci
72 ed polycyclization, and (2) an isomerization-cyclization cascade to generate the remaining bicyclo[3.
73                          A reductive radical cyclization cascade was utilized to build the B ring, an
74 carbocation intermediates that propagate the cyclization cascade, and the chemical strategies that te
75 es of substrate activation that initiate the cyclization cascade, the management and manipulation of
76 d the chemical strategies that terminate the cyclization cascade.
77 diastereoselective aldol/Brook rearrangement/cyclization cascade.
78                     Enantioselective radical cyclization cascades have the potential to deliver compl
79 ctive dearomatizing radical cyclizations and cyclization cascades, triggered by single electron trans
80 ct product groups resulting from alternative cyclization cascades.
81                                   Subsequent cyclization catalyzed either enzymatically by a norcocla
82 d to be unreactive or rearranged under these cyclization conditions.
83 ade itself, incorporating an ensemble of pre-cyclization conformations of the platinum-alkene reactan
84  an alkynophilic Lewis acid in electrophilic cyclization/dealkylation reactions.
85                 All reaction steps including cyclization, dehydration, and oxidation are characterize
86  The highest computed energy barriers at the cyclization-dehydration (17 kcal/mol) and oxidation (21
87 trong support to the mechanism involving the cyclization-dehydration-oxidation sequence of the chromo
88                                  The radical cyclizations deliver new polycyclic hemiaminals or enami
89 C-H activation chemistry and subsequent Heck cyclization delivers the aglycone framework in an overal
90 o ClBcat, failed to mediate the complete the cyclization/demethylation reaction sequence by itself.
91  (de, ee up to >99%) via domino ring opening cyclization (DROC) of activated aziridines with 2-vinyli
92 nvolves a cascade Michael addition-Dieckmann cyclization-elimination sequence, offers rapid and conve
93 erizable E,Z dienyl motif followed by Pinner cyclization enabled the construction of the tetrahydrofu
94 followed by an iron-mediated decarboxylative cyclization event.
95 ombination with a highly efficient "one-pot" cyclization-folding approach, we obtained an RTD-1-based
96 n reaction proceeds via a nucleophilic amino cyclization followed by an intermolecular C-N bond forma
97 em catalysis involving atom-transfer radical cyclization followed by catalytic dehydrohalogenation.
98 mately implemented a sequence of carbazolyne cyclization followed by Rh-catalysed fragmentation to in
99          Control experiments reveal that the cyclization, followed by 1,3-allylic amino dehydroxylati
100  activation that triggered a Vilsmeier-Haack cyclization, followed by an azomethine ylide generation
101 yclization and a titanocene-mediated radical cyclization for the asymmetric assembly of the "AB" ring
102 unsaturated methyl ketone, and (v) a radical cyclization for the cyclobutane ring formation to provid
103 ons with a TMSOTf-catalyzed oxonium-mediated cyclization gave general access to pyrrolo[2,1-a]isoquin
104 ng effect of a remote substituent on radical cyclization has also been presented.
105         A tandem olefin metathesis/oxidative cyclization has been developed to synthesize 2,5-disubst
106 d Bi(OTf)3-catalyzed intramolecular olefinic cyclization has been developed.
107 ably fabricated indoles via C-N bond forming cyclization in 28-82% yield.
108 utions at 3- and other positions followed by cyclization in a domino fashion has been developed.
109 ziridine followed by a concomitant 5-exo-dig cyclization in a domino fashion to furnish the 2-iminoth
110  this study highlights the value of backbone cyclization in directing folding, improving yields, and
111 ryl isothiocynates undergo efficient cascade cyclization in the presence of Ag2CO3 to form indoloquin
112 lating to the mechanism of Garratt-Braverman cyclization in two systems, namely bis-propargyl sulfone
113 ein we describe a novel strategy for peptide cyclization in which intramolecular iminoboronate format
114 ylquinoxaline undergoes irreversible Bergman cyclization indicative of a large retro-Bergman ring ope
115                            Additionally, the cyclization intermediate 3 was isolated, allowing us to
116                                          The cyclizations involve the formation of betaines (imidazol
117              The first dearomatizing radical cyclizations involving radicals derived from amide carbo
118 r benzannelation effectively renders Bergman cyclization irreversible due to favorable aromatic stabi
119                           Photo-mediated 6pi cyclization is a valuable method for the formation of fu
120                     The tail-to-head terpene cyclization is arguably one of the most complex reaction
121                                          The cyclization is diverted from those catalyzed by the char
122  rate, enantio- and site-selectivity for the cyclization is investigated.
123 are competent traps in the bromonium-induced cyclizations, leading to the formation of enantioenriche
124            Optimization of a reductive diene cyclization led to the development of an intermolecular
125 phine sulfide followed by haloalkylation and cyclization led to the enantiomerically enriched tertiar
126                            By optimizing the cyclization linker, length, and amino acid sequence, the
127 lytic cycles involve a concerted or stepwise cyclization mechanism has not been addressed experimenta
128 cally relevant for their exquisite enzymatic cyclization mechanism.
129                                              Cyclization minimizes degradation in the gut, blood, and
130  ambient temperature and the final oxidative cyclization occurs when the substrate is exposed to air
131                                          The cyclization of (2-bromophenyl)pyrrolyl-1,2,4-triazoles v
132                                 Free radical cyclization of (2-bromophenyl)pyrrolyl-1,2,4-triazoles w
133          Fe(acac)3 mediates the deiodinative cyclization of (2-halo)aryloxy furfuranyl ethers, follow
134 dines has been developed using a 6-endo-trig cyclization of (E)-enones.
135            A Bi(OTf)3-catalyzed ring-opening cyclization of (hetero)aryl cyclopropyl carbinols to for
136                       The selectivity of the cyclization of (omega-haloalkyl)alkylarylphosphine deriv
137  a cobalt-catalyzed asymmetric hydroboration/cyclization of 1,6-enynes with catalysts generated from
138 ugh the molecular iodine-catalyzed oxidative cyclization of 2-aminopyridine/amidine and isothiocyanat
139 An acid- and oxidant-promoted intramolecular cyclization of a tetrahydro-beta-carboline-based dipepti
140 ation orientation on C(1)-C(5) and C(1)-C(6) cyclization of acyclic quinoxalenediynes.
141 in) via in situ formation and intramolecular cyclization of alkyl 2-[(2-alkoxybuta-2,3-dienimidoyl)su
142 ydroindolizin-3(5H)-ones from a condensation cyclization of alpha-oxoesters with five- and six-member
143 tion, the study indicates that 6-exo radical cyclization of an alkyl radical to a phenyl ring is fast
144 ective synthesis of this type of compound by cyclization of an aryl bicyclosesquiterpene.
145 as synthesized from dimethoxytetralone 8 via cyclization of an intermediate benzylic radical, generat
146 on the quantitative intramolecular reductive cyclization of an oligo(diyne) with a low-valent zircono
147                     BCl3 -induced borylative cyclization of aryl-alkynes possessing ortho-EMe (E=S, O
148   In this paper, we report an intramolecular cyclization of benzylic-substituted propargyl alcohols p
149                     Metal catalyzed post-Ugi cyclization of bis-amides is reported in this study.
150  CHI activity, which catalyze stereospecific cyclization of both 6'-hydroxychalcone and 6'-deoxychalc
151 -catalyzed intramolecular and stereospecific cyclization of chalcones is a committed step in the prod
152 s are formed, respectively, via 1,5- and 1,6-cyclization of common (5Z)-1,4-diazahexa-1,3,5-triene in
153 tional framework can be used to describe the cyclization of DNA sequences that contain a base pair mi
154                                      For the cyclization of geranyl acetate, it was found that the cl
155                      Due to a fast occurring cyclization of l-glutamine to pyroglutamic acid, the typ
156               A regioselective base-mediated cyclization of mono-N-acylpropargylguanidines is reporte
157  through a palladium-catalyzed carbonylative cyclization of N-(2-iodoaryl)enaminones, proved to inhib
158                           The intramolecular cyclization of N-benzylfumaramide [2]rotaxanes is descri
159 e formation of indazolones by Friedel-Crafts cyclization of N-isocyanates using blocked (masked) N-is
160                               Intramolecular cyclization of nitrogen tethered alkenols catalyzed by p
161  to peptide macrocyclization inspired by the cyclization of non-ribosomal peptide aldehydes is presen
162 zido-iodo-pyranoquinolines via electrophilic cyclization of o-alkynylaldehydes in the presence of sod
163 elective 5-exo-trig intramolecular oxidative cyclization of ortho-cinnamyl phenols using [PdCl2(CH3CN
164 possess a critical pharmacophore (HFRW), and cyclization of peptide agonists often enhances potency.
165             The catalytic, enantioselective, cyclization of phenols with electrophilic sulfenophthali
166                   The method is based on the cyclization of readily available substrates and proceede
167                                Specifically, cyclization of ribbon GeXIVA with a two-residue linker m
168                               Liberation and cyclization of SFTI-1, however, was inefficient, suggest
169 SiH2OO, i.e., the calculated barrier for the cyclization of SiH2OO is only 4.4 kcal/mol, which is nea
170  iodothiophenes, nucleophilic azidation, and cyclization of tetrazolopyrimidines, followed by glycosy
171                                              Cyclization of the amidine-tethered anthranilate then af
172 bacteriochlorin macrocycle, and (ii) Nazarov cyclization of the beta-(propenoyl)-substituted ring C f
173 ine intermediate before the rate-determining cyclization of the hydrazone onto the alkyne group.
174   The key step of synthetic sequence was the cyclization of the latter under Heck reaction conditions
175        Sesterterpene synthase (STS)-mediated cyclization of the linear C25 isoprenoid precursor geran
176 products 2-7 have been prepared by reductive cyclization of the relevant 2-arylcyclohex-2-en-1-one (e
177 diones 2 followed by stereoselective radical cyclization of the resulting adducts 3 to provide the cy
178  arylboronic acid to the alkyne, followed by cyclization of the resulting alkenylnickel species onto
179 ionalization of two ketide units followed by cyclization of the resulting octaketide into tylactone.
180 r both the nonenzymatic and enzyme-catalyzed cyclization of the SpnF substrate.
181 re formed during roasting by dehydration and cyclization of their precursors, the chlorogenic acids (
182 nditions for the subsequent deprotection and cyclization of these intermediates allowed access to pyr
183                   Nickel-catalyzed reductive cyclization of this alkynylaldehyde, to construct the ei
184 ation of the transition state by Ox promotes cyclization of traditionally resistant substrates, broad
185                                The oxidative cyclization of various aldoximes with 1-propene-1,3-sult
186 ase catalyst and selectively accelerates the cyclizations of 4-allen-1-ols into one prochiral allene
187 3 enabled the first catalytic intramolecular cyclizations of carboxylic acid substrates using this Le
188 rtant classes of heterocycles via controlled cyclizations of easily accessible common precursors.
189                  In addition, intramolecular cyclizations of esters enable C-C bond formation as cata
190 s) are responsible for controlling the aldol cyclizations of poly-beta-ketone intermediates assembled
191  Enantioselective nickel-catalyzed arylative cyclizations of substrates containing a Z-allylic phosph
192 lished via palladium(II)-catalyzed oxidative cyclizations of terminal bis(vinylboronate esters).
193 ids to alkynes, followed by enantioselective cyclizations of the alkenylnickel species onto tethered
194  crystallography to understand the effect of cyclization on the electronic properties and structure.
195 hylaluminum chloride followed by a 5-exo-dig cyclization/oxidation reaction catalyzed by copper(II) c
196 nd tetracyclic sesterterpenes, revealing the cyclization path for the pentacyclic sesterterpene (-)-r
197  suggest that these STSs catalyze an unusual cyclization path involving reprotonation, intramolecular
198 the substrate/catalyst interaction along the cyclization path.
199            This stereoisomer induced a novel cyclization pathway leading to sesquiterpenes based on h
200 o understand how the substituent affects the cyclization pathway.
201  radicals can undergo reduction or reductive cyclization pathways, providing a powerful method for (i
202 iosynthetic intermediates toward alternative cyclization pathways.
203 clic urea fused derivatives through a double cyclization process from readily available aminophenyl p
204 d adduct to the aflatoxin system via the Nef-cyclization process was achieved by the assistant of ZnB
205                                         In a cyclization process, Cys residues then attack the dehydr
206 arylation step followed by an intramolecular cyclization process.
207  observed during a reductive radical cascade cyclization process.
208 revealing the general exo-preference for the cyclization processes.
209 a side reaction that afforded an alternative cyclization product, are discussed.
210  enabling access to the otherwise suppressed cyclization product.
211    In addition, further modifications of the cyclization products enabled stereochemistry-function st
212 ly, in the presence of K2CO3, tandem C-C/C-N cyclization products were obtained for a couple of subst
213 iminocarbenes, 1H-azirines, ketenimines, and cyclization products, and 1,2,4-triazoles are precursors
214 ine, via butenylation and diastereoselective cyclization promoted by N,N-dimethyl-4-aminopyridine.
215                   A cross-coupling/reductive cyclization protocol has been employed in a unified appr
216                                The developed cyclizations provide a concise, atom-economical route to
217 generation of iminyl radicals and subsequent cyclization/radical trapping, which allows the effective
218 ecarboxylative pyrimidine/pyridine migratory cyclization (rather than deprotection of pyrimidine/pyri
219                            An intramolecular cyclization reaction leading to the loss of the C-X chai
220                                          The cyclization reaction mechanism and the enantiomeric comp
221                        A tandem deprotection-cyclization reaction of 1,1-diacylcyclopropanes is descr
222                         The halogen-mediated cyclization reaction of aryldiynes to produce halogenate
223 eropyrenes were formed after a 4-fold alkyne cyclization reaction promoted by triflic acid.
224          This work showcases a new catalytic cyclization reaction using a highly Lewis acidic borane
225             An unexpected diastereoselective cyclization reaction was observed, leading preferentiall
226 iterpenoid oxidation activities, including a cyclization reaction, leading to a triterpenoid lactone.
227 bridization during a single enzyme-catalyzed cyclization reaction.
228  MeHg(+) and hCy7 through a mercury-promoted cyclization reaction.
229 zo[b][1,6]naphthyridones via a base-mediated cyclization reaction.
230 a sequential Suzuki-Miyaura coupling/Petasis cyclization reaction.
231 )-Ynamides are converted to oxazolones via a cyclization reaction.
232   The DFT calculation of the iodine-mediated cyclization reactions for molecules containing methoxy,
233 ts efficient and stereoselective dehydrative cyclization reactions from monoallylic diols, with stere
234              Several formal heteroborylative cyclization reactions have been recently reported, but l
235             Novel molecular iodine catalyzed cyclization reactions of 2-amino anilines with aryl alky
236 re is generated by periplasmic oxidation and cyclization reactions of d-tyrosine and l-diaminobutyric
237                                    The first cyclization reactions of enoldiazo compounds with nitros
238   This review aims to provide an overview of cyclization reactions of N-acyliminium ions derived from
239 oach is exploited for multifold C-C coupling cyclization reactions with C-C cleavage using symmetrica
240 iates, also referred to as N-acyliminium ion cyclization reactions, have been employed for the constr
241 yl shift proposed as part of the carbocation cyclization/rearrangement leading to ledol, viridiflorol
242 ent Pictet-Spengler and Bischler-Napieralski cyclization/reduction cascades furnish the cis- and tran
243      Repeated addition of 1 to 4 followed by cyclization resulted in the stereoselective synthesis of
244 lowed by a palladium-catalyzed Mizoroki-Heck cyclization, resulting in selective formation of the exo
245         An alternative fragmentation-radical cyclization sequence of related substrates allows access
246 lic iridoid scaffold in a two-step reduction-cyclization sequence.
247 vage/rotation around the N-C single bond/1,6-cyclization" sequence.
248 , stop, and cysteine-encoding (for disulfide cyclization) sequences.
249   This highly versatile strategy for peptide cyclization should find applications in many areas of ch
250 nial is clearly enzymatically catalyzed, the cyclization step appears to be subject to less stringent
251                           To ensure that the cyclization step is rapid, our design capitalizes on two
252 AmISY is clear, in both AmISY and CrISY, the cyclization step produces a diastereomeric mixture.
253 ne and the indole nucleophile in the initial cyclization step through an intermolecular hydrogen bond
254                           The intramolecular cyclization step was completed in a short time (1-2 h) a
255 tation around C3-C4 and a subsequent thermal cyclization step.
256 emic tropanes were synthesized using Mannich cyclization strategies (Robinson-Schopf and by way of a
257         Mechanistic studies of the reductive cyclization suggest a hydride insertion pathway, explain
258   The key operation is a Pd-catalyzed tandem cyclization that directly establishes the requisite 1,3-
259  switched to an unprecedented formal [5 + 1]-cyclization that provided multifunctionalized 1,3-oxazin
260 that was engaged in MoOPH-mediated oxidative cyclization, then conjugate addition, and redox processe
261 xygen mediated gamma-CH oxidation, a Stetter cyclization to access the pendant cyclopentenone, and a
262 and N-tosyl homoallylamine undergo aza-Prins cyclization to afford (1R,5S,7S)-7-[(benzyloxy)methyl]-2
263 roducts undergo an acid-mediated dehydrative cyclization to arrive at these targets.
264 tro-Bergman ring opening, allowing C(1)-C(5) cyclization to become a competitive reaction channel.
265            Coupled with a late-stage radical cyclization to construct the [3.2.2]-bridged bicycle, th
266 include a Mn(III)-mediated oxidative radical cyclization to construct the trans-decalin ring, and a 6
267 olecule of nitrile followed by electrophilic cyclization to deliver the desired product.
268    4-Pentenylalcohols also undergo oxidative cyclization to form gamma-lactones predominantly.
269                                              Cyclization to form pyrrolidines, piperidines, or morpho
270 ered alkyl/aryl halides that undergo radical cyclization to generate C(sp(3))-Cu complexes in situ, w
271 mote cascade, tandem condensation to oximes, cyclization to nitrones, and 1,3-dipolar cycloaddition t
272 eric C12-fragment (R)-30 underwent reductive cyclization to provide the desired product in 60% yield.
273 atalyst to a Echavarren's gold(I) turned off cyclization to seven member ring and turned on 6-exo-dig
274 om proton-coupled electron-transfer-mediated cyclizations to C-C bond constructions, dehalogenations,
275 sation, cyclopropyl ring opening followed by cyclization took place in a single-pot operation.
276 ynthetic methodologies commonly used for the cyclization toward medium-sized heterocycles cannot be a
277 ased affinity of Au-catalysts to the Bergman cyclization transition state as one of the key component
278 nctionality and a dehydrative intramolecular cyclization under mild conditions to form the oxadiazine
279 mation from readily available precursors and cyclization under mild reaction conditions.
280 r iminoboronate formation allows spontaneous cyclization under physiologic conditions to yield monocy
281 mides could undergo intramolecular oxidative cyclization under the optimized conditions to give isoin
282 on, tandem hydrogenation/hydrogenolysis, and cyclization upon reaction with 4-bromobutanal to give th
283 e, and methane-toward Garratt-Braverman (GB) cyclization using density functional theory calculations
284 undergoes decarboxylative pyridine migratory cyclization using MeOTf/NaOMe in toluene providing 6-met
285 catalyzed by Re2O7, followed by an oxidative cyclization using the above Pd catalyst, is performed.
286                                              Cyclization via a thiolactone bond is essential for AIP
287 matic ring at the activated triple bond, and cyclization via an exclusive 6-endo-dig process.
288                                      Bergman cyclization via thermal activation of these constructs y
289 cloaddition and subsequent template-directed cyclization via Yamamoto coupling.
290 d reduction of amides and reductive umpolung cyclizations via aminoketyl radicals as a key step.
291 derivatives through ring opening followed by cyclization (vinylcyclopropane-cyclopentene rearrangemen
292                    A three-component cascade cyclization was developed to synthesize 2,3-diarylisoind
293             The base-mediated intramolecular cyclization was found to be general for both alkyl- and
294 gement in diastereoselective Pictet-Spengler cyclization were the key steps.
295 he final step involved a highly unusual Heck cyclization whereby ligand control enabled efficient for
296 zed radical cyclization, and a double 6-endo cyclization with catalyst loadings as low as 0.01 mol%.
297 yl vinyl ketones that undergo facile Nazarov cyclization with excellent chemo-, regio-, and stereocon
298 ctive pseudo-four-component tandem oxidative cyclization with fragmentation from a 1,3-dicarbonyl com
299 atic reaction suggest a similar mechanism of cyclization within the enzyme active site; however, ther
300 tory studies on photoredox-catalyzed radical cyclizations yielded interesting results, including the

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