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1 eterochiral molecules (one of them involving cyclization).
2  a highly diastereoselective Pictet-Spengler cyclization.
3 nd its subsequent intramolecular aza-Michael cyclization.
4 ituted trienes that are resistant to thermal cyclization.
5 s well as increased control over the rate of cyclization.
6 ive C(7)-H functionalization and concomitant cyclization.
7 mines and their subsequent fragmentation and cyclization.
8 ole as the nucleophilic partner in the first cyclization.
9 cluding polysubstituted olefin formation and cyclization.
10 itions, specifically the degree of core GDGT cyclization.
11 e formation of a 1,4-diradical by an initial cyclization.
12 noline-, and quinoline ynones, via 5-exo-dig cyclization.
13 talytic cycle via intramolecular dehydration/cyclization.
14 ectrocyclic mechanism analogous to a Nazarov cyclization.
15 enantioselective Morita-Baylis-Hillman (MBH) cyclization.
16 ic attack by pyridyl nitrogen results in its cyclization.
17 lable and could also be applied to a cascade cyclization.
18 h undergoes spontaneous transannular Mannich cyclization.
19 enamine intermediate followed by 1,5-exo-dig cyclization.
20 stereoselectivity resulting from the radical cyclization.
21 th boronic acids, followed by intramolecular cyclization.
22 droxyaspartic acid ligation-mediated peptide cyclization.
23 ilability, in influencing the degree of GDGT cyclization.
24  vinylogous alpha-amido radical formed after cyclization.
25 thoxyaryl)propiolates for thiocyanative ipso-cyclization.
26 intermediates that readily engage in Nazarov cyclizations.
27 re development of asymmetric 2-imino-Nazarov cyclizations.
28 inium ions that undergo Pictet-Spengler-type cyclizations.
29 ase-mediated Michael addition/intramolecular cyclization/[1,5]-H shift/cleavage of CS(2)/aromatizatio
30 yzed propargyl Claisen rearrangement/Nazarov cyclization, a [4+2] cycloaddition of the formed six- or
31         Via an intramolecular Friedel-Crafts cyclization, a dihydrobenzofuranone was obtained.
32 y peptides that could benefit from bioactive cyclization, a strategy that is amenable to broad applic
33 tive sites in the C and T domains diminished cyclization activity of GliP in vitro and abolished glio
34                                        The N-cyclization-alkylation cascade introduces a novel retros
35                                          The cyclization also proceeds with tosylamides forming C-N b
36                  However, the extent of this cyclization also varies with growth phase and electron a
37 e reaction undergoes feasible steps that are cyclization and 1,2-H shift before elimination to persis
38 se events, which included a unique Conia-ene cyclization and a challenging Pauson-Khand reaction, aff
39  reaction appears to proceed via a Dieckmann cyclization and a retro-aldol elimination, releasing amm
40 )/CeO(2) greatly enhances the selectivity of cyclization and aromatization in the n-hexane reforming
41 vity of single-site Pt(1)/CeO(2) toward both cyclization and aromatization is above 86% at 350 degree
42 nism underpinning the complex process of GPA cyclization and furthermore show the utility of the tech
43                      We also showed that the cyclization and ligation of peptides and proteins with v
44 molecules that are capable of both efficient cyclization and of pre-organizing another precursor to e
45  by an intramolecular 1,6-conjugate addition/cyclization and oxidation sequence.
46        The role of NHC in the intramolecular cyclization and preliminary mechanistic experiments are
47 st control through stereoselective oxidative cyclization and subsequent, stereospecific allyl-isomeri
48 from a nonaromatic enediyne core via Bergman cyclization and Suzuki-Miyaura coupling of the resulting
49 roso-intermediate are proposed for oxidative cyclization and the unexpected intermolecular displaceme
50 P is discussed, including their formation by cyclizations and oligomerizations of aldehydes and creat
51 ade involving Cope rearrangement, 6-exo-trig cyclization, and a final electrophilic aromatic substitu
52  This approach allowed one-pot deprotection, cyclization, and deselenization to give several differen
53  formation, Michael addition, intramolecular cyclization, and intramolecular iminium ion cyclization
54 -hydrogen atom translocation, intramolecular cyclization, and rearomatization steps lead to valuable
55 yzed sequences involving oxidative addition, cyclization, and termination through intermolecular nucl
56 plexity-building Mannich reaction, efficient cyclizations, and a highly diastereoselective hydrogenat
57 and stereoselective intramolecular oxidative cyclization; and (c) a complexity-generating aza-Cope/Ma
58 ole and (ii) a three-step cross-coupling and cyclization approach starting from the zincated 4,6-dich
59 embered enediynes' reactivity in the Bergman cyclization are also reported.
60 atalyst-controlled intra- and intermolecular cyclizations are mainly described to give five- and six-
61 rted solid-state topochemical polymerization/cyclization-aromatization strategy to convert the simple
62 n of these N-oxides enabled a formal Cadogan cyclization at room temperature for 2 H-indazole synthes
63 ransformation involving two independent peri-cyclizations at the central core.
64             A mechanism is proposed for this cyclization based on DFT calculations.
65          We also reveal the mechanism of the cyclization based on DFT modeling and obtain a clear cor
66 enyl)isoquinoline-2-oxides via electrophilic cyclization between alkynylbenzaldoximes and diorganyl d
67 esults support the hypothesis that oxidative cyclization between amino acid nitrogen and the prenyl c
68 ns, this observation suggested that the 3',8-cyclization by MoaA is accelerated by 6-9 orders of magn
69  synthetic strategies including head-to-tail cyclization (C1), side-chain-to-tail cyclization (C2), a
70 to-tail cyclization (C1), side-chain-to-tail cyclization (C2), and a disulfide bond cross-linkage (C3
71                                          The cyclization can also be extended to the formation of six
72  An efficient two-component copper-catalyzed cyclization cascade approach toward highly functionalize
73  the synthesis of such structures by radical cyclization cascade reactions is rare.
74 etic pathways: the multibond-forming polyene cyclizations catalyzed by the yet poorly understood fami
75 dem, microwave-assisted oxyanionic 6-exo-dig cyclization/Claisen rearrangement reaction.
76 ly catalyzes the highly selective 6-endo-dig cyclization, completely reversing the regiochemistry tha
77 nation and diastereoselective Friedel-Crafts cyclization constitute an efficient synthetic route to a
78   Synthesis of bridged scaffolds via Type II cyclization constitutes substantial challenges due to th
79                           The degree of GDGT cyclization correlated with growth rate under most condi
80 de product formed through 4-exo-trig radical cyclization could be recycled through an unprecedented t
81                    An alkoxycarbonyl radical cyclization-cross-coupling cascade has been developed th
82 chnical issues for converting the FRET-based cyclization/decyclization rates to an equilibrium quanti
83 ds affect these one-pot aza-Michael-addition/cyclization/dehydration reaction sequences.
84 xypropenones, which can also undergo Nazarov cyclization, delineation between competing Nazarov and C
85 rate as well as a one-pot Rieche formylation/cyclization/deprotection sequence to efficiently constru
86                 It is shown that consecutive cyclizations do not involve brominated intermediates and
87  that of alpha-RgIA4, demonstrating that the cyclization does not perturb the overall conformation of
88 ve S-alkylation followed by intramolecular N-cyclization enabling the formation of C-S and C-N bonds
89  reduction triggers a regioselective radical cyclization event, followed by anion formation and quenc
90 y-indoles that trigger facile intramolecular cyclization followed by an oxidative quenching step.
91  a Z-selective ring-closing metathesis (RCM) cyclization followed by an oxygen to carbon ring contrac
92 n alkanethiol to an isonitrile moiety, 5-exo cyclization, followed by nucleophilic addition of an alk
93                A one-pot, metal-free, double cyclization for the synthesis of bicyclic 2-pyridones as
94 rature atroposelective intramolecular S(N)Ar cyclizations for sequential CD (8:1 dr) and DE ring clos
95 activated aldehydes followed by alkyne-Prins cyclization, Friedel-Crafts reaction, and final eliminat
96 ls-Alder (IMDA) and hetero-Diels-Alder (HDA) cyclizations from an ambimodal transition state, as well
97  benzylic gem-diboronates, via radical carbo-cyclization/gem-diborylation of alkynes with a high func
98 lowed by azidation, thermal or photochemical cyclization, glycosylation, and final functionalization
99 he proline-catalyzed direct Mannich reaction-cyclization/IBX-mediated site-selective oxidation/NaBH(4
100 tD is competent to perform an intermolecular cyclization in addition to its cognate intramolecular re
101            The results suggest the degree of cyclization in archaeal lipids records a universal respo
102 ne frameworks via thio(seleno)cyanative ipso-cyclization in the presence of ceric ammonium nitrate (C
103 ulations show that the reaction proceeds via cyclization in the triplet excited state to yield a 1,4-
104  are regioselectively favoring the 5-exo-dig cyclizations in all the annulation processes.
105 n selected such as inter- and intramolecular cyclizations, including carba-, oxa-, thia- and oxazacyc
106 Here we show that the average degree of GDGT cyclization increases with doubling time in continuous c
107                  Subsequent enantioselective cyclization involving a BOX-ZnI(2)-activated alkyne lead
108 bond protonation, followed by intramolecular cyclization involving the interaction of the carbocation
109    The development of new one-pot sequential cyclizations involving a Vilsmeier-Haack reaction follow
110 tational results supported the idea that the cyclization is a 4pai-electrocyclization and not a 5-end
111 vacine and ellipticine via late-stage D-ring cyclization is described.
112 sized in a modular fashion but also that the cyclization is efficient and amenable to the presence of
113                                    The final cyclization is incompatible with this mechanism and is f
114  cyclization pathways support that the 5-exo cyclization is preferable.
115 he preparation of indolines by dearomatizing cyclization is presented.
116 the rate controlling step, (b) excited state cyclization is the rate controlling step, and (c) the ra
117 nus not bearing a phenyl ring is because the cyclization is thermodynamically disfavorable, subsequen
118 d in order to undergo further intramolecular cyclization leading to a new class of macrocycle.
119 undergo triflic acid-mediated intramolecular cyclization, leading to benzo[b]fluorenone derivatives v
120                                              Cyclization linker optimization from library screening p
121                            Here, we measured cyclization (looping) and decyclization (unlooping) rate
122 mputations identified a barrierless two-step cyclization mechanism for the formation of 2 upon photoe
123 rins are synthesized by employing the Scholl cyclization method.
124           Catalytic enantioselective Type II-cyclization methods are even rarer.
125 ty obtained through the preferred 5-exo-trig cyclization mode.
126 a radical-polar crossover mechanism, and the cyclization occurs by nucleophilic attack of a convenien
127           Using a stable precursor to start, cyclization occurs via a catalytic controlled process.
128 atalyzed, carbon monoxide mediated reductive cyclization of 1,4-dialkenyl-2,3-dinitrobenzenes.
129 nt-theory investigation of the formation and cyclization of 2'-alkynylacetophenone oxime radical cati
130  of substituent effects on the formation and cyclization of 2'-arylbenzaldehyde and 2'-arylacetopheno
131 ry alcohols and acceptorless dehydrogenative cyclization of 2-aminobenzyl alcohol with ketones throug
132 hrough the iodine-mediated [3 + 2] oxidative cyclization of 2-aminoheteroarenes and isothiocyanates/i
133 We report here the regioselective 6-endo-dig cyclization of [2-(butylselanyl)phenyl]propynols promote
134 oth approaches, the key step is based on the cyclization of a (tris)lithio-triphenylmethane or a (tri
135 effecting a transannular C20-C2 free radical cyclization of a challenging substrate with formation of
136 on of the C-9/C-14 bond by a SmI(2)-mediated cyclization of a keto aldehyde.
137                         An intricate radical cyclization of a late stage intermediate followed by an
138 tic strategy also features an intramolecular cyclization of a N-chloroamine to forge the C6-N bond, a
139                                          The cyclization of a series of nonheterocyclic allenyl aryl
140  that NanA-C(T) catalyzes the regioselective cyclization of a surrogate synthetic substrate, Ant-l-Ky
141 2-trihydro[3]triangulenium cation by cascade cyclization of a tetra-benzyl alcohol precursor in trifl
142 reaction conditions were then applied to the cyclization of a tripeptide and an arodyn analog resulti
143    The reaction proceeds through the cascade cyclization of acylimines (in situ formed) with activate
144 was played by the cobalt-catalyzed oxidative cyclization of alken-5-ol derivatives ("Mukaiyama cycliz
145 yzed enantioselective intramolecular Type II cyclization of alkynes via C-C activation of cyclobutano
146  THF rings is then believed to occur through cyclization of an alcohol/alkoxide to the recently forge
147                                 Epoxypolyene cyclization of an enantiomerically pure, but geometrical
148 ction conditions, followed by intramolecular cyclization of an intermediate formed after the regenera
149 of 15 R-HETE but also allows oxygenation and cyclization of arachidonic acid to a 15 R-PG endoperoxid
150 monstrated via site-selective intramolecular cyclization of aryl-fused 1,6-diyn-3-ones.
151 /DBU/MS joint system-catalyzed carboxylative cyclization of arylacetylene, arylaldehyde, and arylamin
152               An Ir(III)-catalyzed oxidative cyclization of benzoic acids with propargyl alcohols to
153          Key steps involve the (i) Vollhardt cyclization of bis(propargyl)benzenes with bis(trimethyl
154                              A corresponding cyclization of C-phenylnitrile imine 19 can also lead to
155 nt dimerization specifically accelerates the cyclization of cGAMP.
156 triguing observations in the Au(I)-catalyzed cyclization of cyclic and acyclic acetals of alkynylalde
157                                              Cyclization of DNA with sticky ends is commonly used to
158                 An asymmetric hydroarylative cyclization of enynes involving a C-H bond cleavage is r
159 a method for its formation by intramolecular cyclization of ester-tethered enaminones, which can easi
160         MoaA catalyzes an unprecedented 3',8-cyclization of GTP into 3',8-cyclo-7,8-dihydro-GTP (3',8
161 n pathway involves an intramolecular cascade cyclization of homopropargyl sulfonamides to generate a
162       This process is also applicable to the cyclization of internal alkyne-tethered N-propargylic be
163                                              Cyclization of linear dipeptidyl precursors derived from
164 ation reactions, specifically, a dehydrative cyclization of monoallylic diols for the synthesis of th
165 le as the best precatalyst for the oxidative cyclization of N-alkenylamides into 2-oxazolines.
166                       A metal-free oxidative cyclization of N-Boc-acrylamides with (diacetoxyiodo)ben
167 ctional theory and CASPT2 levels now examine cyclization of N-phenylnitrile imine 13 to indazole 17.
168  key step of the synthetic sequence included cyclization of N-protected 2-(azetidin-3-yl)propane-1,3-
169   The observed regioselectivity of the ortho-cyclization of nitroso oxides was explained using theore
170 the utility of the technique for probing the cyclization of non-natural GPA peptides by these powerfu
171 oxime-catalyzed acceptorless dehydrogenative cyclization of o-teraryls was developed.
172 an indium-catalyzed intramolecular 5-exo-dig cyclization of ortho-alkynyl diketopiperazines has been
173                           We now report that cyclization of pivaldimino-amides with phosgene in the p
174 s-electrophilic agents and their use for the cyclization of proteins.
175 ) derived reagent (c-PyPA) obtained from the cyclization of pyrophosphate with a reactive diisopropyl
176 ted cascade process was developed, involving cyclization of readily available beta-ketonitriles into
177       These can be described in terms of the cyclization of six {Fe(3)Ln(muOH)(ampd)(2)(Hampd)(2)(PhC
178 ient conditions through tandem oxidation and cyclization of sp(3) C-H bonds under metal-free conditio
179                                   Sequential cyclization of substrates with ester groups could be ach
180  of the OxyE enzyme in maintaining effective cyclization of such peptides bearing 3,5-dihydroxyphenyl
181 ep of the proposed strategy is base-mediated cyclization of sulfonamide-tethered 5-iodo-1,2,3-triazol
182                                         Upon cyclization of the Barbier product to lactam and enolate
183 .1.1]hexane 2,2-dioxide) were synthesized by cyclization of the corresponding amino sulfonyl fluoride
184 vealed significant effects of the structural cyclization of the D-A-repeating unit, including more ef
185  the benzazepine scaffold, while spontaneous cyclization of the dipeptide yielded the alternative kin
186 none (E, 70%; Z, 3%); subsequent double-ring cyclization of the E-enone (via Nazarov, electrophilic a
187 n that is required for reductive release and cyclization of the NRPS-tethered dipeptidyl-thioester in
188                       A strong acid promotes cyclization of the Os(VI) dioxoglycolate, or its NMO com
189  cysteine residues, resulting in the in situ cyclization of the protein (INCYPRO).
190 d nitrite reagent-mediated diazotization and cyclization of the subsequent 1,2-aryldiamines as the ke
191  NanA are responsible for the regioselective cyclization of the tethered Ant-l-Kyn dipeptide to form
192             An acid-catalyzed intramolecular cyclization of three such indolines gave tetracyclic lac
193 C-terminal residue Ser(33) cleavage, and the cyclization of ToPI1 via a peptide bond between residues
194 trimethylsilyl)amide-mediated intramolecular cyclization of trisubstitued cyclopentane carboxylates b
195 ampestris into a monooxygenase for oxidative cyclization of tryptophans.
196 opy, support a mechanism involving oxidative cyclization of two dienes that determines regio- and dia
197 trary, 2,6-dialkylpyridines were produced by cyclization of unsaturated ketones.
198 omputational data supporting the notion that cyclizations of 3-halopentadienyl cationic intermediates
199 acid catalyst exerts control over asymmetric cyclizations of acyclic ketone-derived trisubstituted ox
200 nds promote highly enantioselective aza-Heck cyclizations of alkenyl N-(tosyloxy)carbamates.
201       Several additional examples of cascade cyclizations of alpha,beta-unsaturated thioesters procee
202  for the reduction of epoxides and for 5-exo cyclizations of suitably unsaturated epoxides.
203 ll as more thermodynamically favorable, than cyclizations of the analogous 3-oxypentadienyl cationic
204 age complex can catalyze oxa-Pictet-Spengler cyclizations of tryptophols and various aldehyde derivat
205 reaction proceeds via a novel Dieckmann-like cyclization pathway.
206 d relative free energies of 5-exo and 6-endo cyclization pathways support that the 5-exo cyclization
207 milar residues in peptide and peptidomimetic cyclizations performed on solid phase.
208 th range of 360-410 nm, whereas the E-isomer cyclization (Phi(c) = 0.006-0.008) and cycloreversion (P
209 isomerization (Phi(ZE) ~ Phi(EZ) ~ 0.30) and cyclization (Phi(c) = ~0.07).
210              We have found not only that the cyclization precursors can be synthesized in a modular f
211                                          The cyclization precursors were equipped with propargylic OM
212                                          The cyclization precursors were prepared by a double Kosugi-
213                                 Unsymetrical cyclization precursors were prepared by two sequential c
214 no benzyl alcohols followed by NHC-catalyzed cyclization proceeding via the imidoyl azoliums under ox
215                          The Cp*Ru-catalyzed cyclization proceeds well with both simple alkynyl triaz
216 i-4CR adducts, employing an aromatic radical cyclization process promoted by tetrabutylammonium persu
217  ketimine addition, and Pictet-Spengler-like cyclization processes and affords products in up to 92%
218 onitroalkenes via a cascade Michael addition-cyclization protocol to afford nitrodihydrofurans and hy
219 uinone to the prochiral radical formed after cyclization provides high levels of enantioselectivity a
220  As the iminium ion undergoing the aza-Prins cyclization rapidly isomerized to a planar enamine inter
221 -soluble species, and increased control over cyclization rate.
222 metal-free, simultaneous triple C-C coupling cyclization reaction between phenacyl bromides and indol
223 3-dicarbonyl compounds followed by Conia-ene cyclization reaction in moderate to good yields catalyze
224  detailed computational investigation of the cyclization reaction mechanism suggests facile C-N bond
225                                The amination cyclization reaction mechanism was examined employing nu
226 ighly robust one-pot, four-component cascade cyclization reaction of alpha-keto aldehydes, anilines,
227 s the only reagent for the unusual and rapid cyclization reaction to furnish all new carbazole compou
228 tive phase-transfer-catalyzed domino Michael-cyclization reaction with acetylacetone.
229 ucial in the final stage of the head-to-tail cyclization reaction, but the enzyme(s) involved in the
230 rona discharge, solvent-free Borsche-Drecsel cyclization reaction, Katritzky chemistry, and Paal-Knor
231 ormation, and ESI-MS analyses of the ongoing cyclization reaction.
232 ium complex with HFIP which may initiate the cyclization reaction.
233  of hongoquercins using gold-catalyzed enyne cyclization reactions and further derivatization are des
234 wn to catalyze enantioselective tail-to-head cyclization reactions of neryl chloride analogues.
235 is was designed featuring two gold-catalyzed cyclization reactions, specifically, a dehydrative cycli
236 ry centres induce large rate enhancements in cyclization reactions-known as the Thorpe-Ingold effect-
237      Thorough optimization of the activation/cyclization resulted in yields ranging from 15 to 85% fo
238  two-step catalytic asymmetric reduction and cyclization sequence from ketone enolate-derived adducts
239 erization and an amidation/N-acyliminium ion cyclization sequence to furnish four of the five requisi
240  one-pot rhodium catalyzed N-H insertion and cyclization sequence uses diazo compounds to stitch toge
241  C-H alkylation and intramolecular oxidative cyclization sequence.
242  position changes the direction of the ortho-cyclization so that it occurs via the cis/anti form of n
243 d determined the rate of the on-pathway 3',8-cyclization step as 2.7 +/- 0.7 s(-1).
244 d heterochiral cross-coupling with a Bergman cyclization step have been examined.
245 he potential energy surface reveals that the cyclization step is a key step controlling the selectivi
246    Participation of the uracil moiety in the cyclization step is proposed.
247                                    The final cyclization step was shown to be a transformation amenab
248  strongly supports a radical process for the cyclization step.
249  cyclization, and intramolecular iminium ion cyclization steps.
250 he initial reductive coupling and subsequent cyclization steps.
251 ith less double-bond isomerization and fewer cyclization steps.
252  regioselective gold(I)-catalyzed 6-endo-dig cyclization strategy for the construction of the isocoum
253  A tandem acetylene-activated S(N)Ar-anionic cyclization strategy is presented for the synthesis of c
254                                  An on-resin cyclization strategy was employed to prepare A5A(1) anal
255 es from o-phenylenediamines via an oxidative cyclization strategy.
256 iodo aryl allenyl ethers initiates a radical cyclization that is followed by intermolecular radical-r
257    After selective hydrolysis and subsequent cyclization, the phosphonate or phosphinate intermediate
258                      In Sez-mediated peptide cyclization, the Sec can also be retained, which enhance
259  it becomes potentially competitive with the cyclization to 1 H-diazirines and hence rearrange to car
260  or cesium carbonate, underwent nucleophilic cyclization to afford 4-methylene-3-[(4-nitrophenyl)thio
261 w conditions with a subsequent base-mediated cyclization to afford the desired substituted indoles.
262                  Montmorillonite K10 favored cyclization to bicyclononane.
263 t sequence of lactam reduction and aza-Prins cyclization to directly set the final stereogenic center
264 meworks and the base-mediated intramolecular cyclization to establish the spiral quaternary center of
265 es domino imine formation and intramolecular cyclization to form 2-arylcyclopropyl-2,3-dihydroquinoli
266 wed by an aerobic, copper-catalyzed, radical cyclization to form Csp(2)-Csp(2) and O-Csp(2) bonds.
267 e dimethyl acetal, followed by acid-mediated cyclization to generate the iminium precursor that was s
268 l bromide, finally leading to intramolecular cyclization to give a mixture of diastereomers with exce
269                                              Cyclization to II and III produced submicromolar AR anta
270 oles and rhodium-catalyzed ring-opening, and cyclization to N-difluoromethylated oxazoles and thiazol
271 dation and dehydration occur not only during cyclization to pGlu, but also during other reactions lea
272 of epoxypolyenes-substrates that can undergo cyclization to podocarpane-type tricycles-reveals relay-
273 ilding of the pyrrolo nucleus, and reduction-cyclization to the corresponding diazepine.
274 ondensation with aminoalcohol, and oxidative cyclization to the target pyrrole ring.
275 lis (VRE), and another undergoes spontaneous cyclizations to a cyclopropane-bridge-containing hexacyc
276 e enzymes can catalyse redox-neutral radical cyclizations to produce enantioenriched oxindoles from a
277 s for stereo- and regiochemical transannular cyclizations to synthesize three different indolizidin-2
278 ) chelate; the reaction proceeds via Nazarov cyclization (to form the isocyclic ring), S(E)Ar (to con
279 imethylacetals required for Pomeranz-Fritsch cyclization under sufficiently mild conditions to prepar
280 nyl-5-pentyn-1-ols fail to undergo 6-exo-dig cyclization under the conditions employed.
281 rdeveloped affinities and could benefit from cyclization using a bridging linker sequence.
282  Here, we report an enantioselective radical cyclization using alkyl iodides as precursors to unstabi
283 matically generates, evaluates, and proposes cyclizations utilizing a library of well-established che
284 ed rings through spiroannulation followed by cyclization via C-H activation.
285         The crucial step of the synthesis is cyclization via nonclassical Wittig olefination of resin
286  also catalyse reductive dehalogenations and cyclizations via single electron transfer mechanisms.
287            A novel Co(II) -catalyzed polyene cyclization was developed that is uniquely effective whe
288     The regioselectivity of the transannular cyclization was influenced by amine protection to favor
289                     Oxidation-dependent NDGA cyclization was required for the interaction with monome
290 rability of an S(N)Ar-like mechanism for the cyclization was supported by DFT calculations.
291 dimethyl group to promote both stability and cyclization, we found the initial rate of payload releas
292 hermodynamics and kinetics of radical cation cyclization, we provide an explanation for these observa
293 ved from (+)-vince lactam, resulted in 5-exo cyclizations which furnished a series of 2,5-dimethyl-1-
294 zation of alken-5-ol derivatives ("Mukaiyama cyclization"), which is shown to be exquisitely chemosel
295 erization or through a Pomeranz-Fritsch-type cyclization with a final intramolecular Heck reaction.
296  E upon Knoevenagel condensation and Nazarov cyclization with a ring D constituent as demonstrated in
297 ulfonic acid (PTSA)-catalyzed intramolecular cyclization with aldehydes has been developed.
298                                    Rather, a cyclization with subsequent hydrogen abstraction occurre
299 des inter- and intramolecular buta-1,3-diyne cyclizations with the formation of iodoethynylheterocycl
300               ASA can undergo intramolecular cyclization, yielding an equilibrium with the resulting

 
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