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1 electrophilic substitution and as dienes in Diels-Alder cycloaddition.
2 e highly populated, thereby facilitating the Diels-Alder cycloaddition.
3 ng it to undergo a subsequent intramolecular Diels-Alder cycloaddition.
4 idine-modified RNA molecules that catalyse a Diels-Alder cycloaddition.
5 ki-Miyaura cross-coupling reactions and in a Diels-Alder cycloaddition.
6 nalized substrate of SdnG for intramolecular Diels-Alder cycloaddition.
7 e core via an intramolecular cyclopentadiene-Diels-Alder cycloaddition.
8 ions used to functionalize fullerenes is the Diels-Alder cycloaddition.
9 formed by Horner-type Wittig reactions and a Diels-Alder cycloaddition.
10 followed by an intramolecular inverse-demand Diels-Alder cycloaddition.
11 key intermediate, followed by intramolecular Diels-Alder cycloaddition.
12 uent spontaneous intramolecular [4+2] hetero-Diels-Alder cycloaddition.
13 en participate in a second stage acylnitroso Diels-Alder cycloaddition.
14 uct of which is immediately intercepted by a Diels-Alder cycloaddition.
15 rbaldehyde motif that is inaccessible by the Diels-Alder cycloaddition.
16 on, alkene isomerization, and intramolecular Diels-Alder cycloaddition.
17 = Br) is obtained through a cobalt-catalyzed Diels-Alder cycloaddition.
18 l likely be as useful as, the intramolecular Diels-Alder cycloaddition.
19 e highly populated, thereby facilitating the Diels-Alder cycloaddition.
20 acids in room temperature, enantioselective Diels-Alder cycloadditions.
21 bstrates for silicon-tethered intramolecular Diels-Alder cycloadditions.
22 approach in ca. 90 % of Michael additions or Diels-Alder cycloadditions.
23 ent dienophiles in inter- and intramolecular Diels-Alder cycloadditions.
24 pontaneously undergo stereoselective [2 + 4] Diels--Alder cycloadditions.
25 e highly populated, thereby facilitating its Diels-Alder cycloaddition across a tethered benzofuran.
26 alkenes in polar solvents proceeds through a Diels-Alder cycloaddition along the C-C axis (C3/C6 cycl
28 es an intramolecular inverse electron-demand Diels-Alder cycloaddition and a stereoselective Giese ra
29 assembled using a tandem phenolic oxidation/Diels-Alder cycloaddition and a tandem 5-exo-trig/5-exo-
30 dem Knoevenagel condensation, formal [4 + 2]-Diels-Alder cycloaddition and acid catalyzed oxazine rin
31 reoselective intermolecular photoenolization/Diels-Alder cycloaddition and an alkoxy-radical-induced
32 skeletal frameworks using hydroxyl-directed Diels-Alder cycloaddition and reductive N-N bond cleavag
33 lude a 1,3-dioxa-2-silacyclohexene templated Diels-Alder cycloaddition and type-3 semipinacol rearran
34 epared from 2,3-dimethyl-1,3-butadiene using Diels-Alder cycloadditions and Pd(0)-catalyzed coupling
35 ift-aldol cascade reaction, an exo-selective Diels-Alder cycloaddition, and a late-stage Fleming-Tama
36 ations were synthesized from muconic acid by Diels-Alder cycloaddition, and copolymerized with hexame
37 able tetrahydroquinoline linkage through aza-Diels-Alder cycloaddition, and finally, the covalent inc
38 gen, a 6pi electrocyclic ring-opening, and a Diels-Alder cycloaddition, and proceeds with excellent s
41 a transition-metal catalyzed intramolecular Diels-Alder cycloaddition-aromatization cascade construc
42 tituents at their 3- and 6-positions undergo Diels-Alder cycloaddition as a 2-azadiene component with
44 ructures representing Diels-Alder and hetero-Diels-Alder cycloadditions as well as a sigmatropic rear
45 2)-CATPHOS is the result of a regioselective Diels-Alder cycloaddition between 1,4-bis(diphenylphosph
46 ecture of H-KITPHOS is constructed via [4+2] Diels-Alder cycloaddition between 1-(dicyclohexylphosphi
47 azaoctane structures using an intermolecular Diels-Alder cycloaddition between a pyrazinone and comme
48 t chamaecypanone C have been synthesized via Diels-Alder cycloaddition between the cyclopentadienones
51 nvergent synthetic approach involves initial Diels-Alder cycloaddition between two unstable component
54 ctivation volumes of force-accelerated [4+2] Diels-Alder cycloadditions between surface-immobilized a
55 an enantioselective inverse-electron-demand Diels-Alder cycloaddition, C-O bond formation to assembl
56 Yamamoto-type cyclization followed by 6-fold Diels-Alder cycloaddition, C216 was obtained by oxidativ
57 eimides are used, maleimide deprotection and Diels-Alder cycloaddition can be simultaneously carried
58 bled through a one-pot Stille/intramolecular Diels-Alder cycloaddition cascade to construct the core
59 miempirical calculations of the transannular Diels-Alder cycloaddition cascade were carried out to de
60 and stereoselective domino Pauson-Khand and Diels-Alder cycloaddition catalyzed by [RhCl(CO)2]2 unde
61 sful approaches include strategies featuring Diels-Alder cycloadditions, Cope rearrangement, divinyl
62 egiocontrolled "click-unclick" oxazole-ynone Diels-Alder cycloaddition/cycloreversion and ensuing 2-a
65 e C70 derivative were synthesized by using a Diels-Alder cycloaddition followed by an addition-elimin
66 rom D-galactose via Eastwood olefination and Diels-Alder cycloaddition, followed by a mild electroche
68 NX, 4) were synthesized utilizing asymmetric Diels-Alder cycloadditions for the construction of the n
69 cute a highly stereoselective intramolecular Diels-Alder cycloaddition, forming the hydroisobenzofura
71 ate dimer 6, which on intramolecular [4 + 2] Diels-Alder cycloaddition gave an unexpected spirochlori
73 Bioorthogonal inverse-electron-demanding Diels-Alder cycloadditions (iEDDA) were conducted on the
74 ated an autoxidation reaction, followed by a Diels-Alder cycloaddition in the presence of electron-de
75 ich predict that the activation energies for Diels-Alder cycloadditions in the bay regions of periace
76 y a chiral phosphoric acid catalyzed Nitroso-Diels-Alder cycloaddition involving [(1E,3E,5E)-hexa-1,3
78 s at accelerating an inverse electron demand Diels-Alder cycloaddition is directly correlated with it
82 photoredox catalysis of radical cation based Diels-Alder cycloadditions mediated by the first-row tra
83 synthesis of several benzonorbornadienes by Diels--Alder cycloaddition of cyclopentadiene derivative
87 4 portion of gymnodimine was synthesized via Diels-Alder cycloaddition of a 1,2,3-trisubstituted dien
89 ne were accomplished using an intramolecular Diels-Alder cycloaddition of a furanyl carbamate as the
90 based on a proximity-induced intramolecular Diels-Alder cycloaddition of a transient ortho-quinone d
91 ainic acid, through a high-pressure-promoted Diels-Alder cycloaddition of a vinylogous malonate deriv
94 abicyclic adduct formed by an intramolecular Diels-Alder cycloaddition of an amidofuran with a cycloh
96 r pericyclic reactions, including the parent Diels-Alder cycloaddition of butadiene with ethylene, el
98 SbF6 the resulting Lewis acids catalyzed the Diels-Alder cycloaddition of cyclopentadiene and methacr
99 asymmetric Lewis-acid organocatalysis of the Diels-Alder cycloaddition of cyclopentadiene to cinnamat
101 actones 29 and 30, which originated from the Diels-Alder cycloaddition of Danishefsky's diene to (5S)
103 mplexes promote the efficient radical cation Diels-Alder cycloaddition of electron-rich dienophiles u
105 The reaction proceeds via a tandem hetero-Diels-Alder cycloaddition of N,N'-bis(benzenesulfonyl)su
108 rgoes post-assembly modification (PAM) via a Diels-Alder cycloaddition of the anthracene panels of th
109 lded conformation of these C-N atropisomers, Diels-Alder cycloaddition of the isoindole is achieved w
110 e 1 forms a unique covalent adduct through a Diels-Alder cycloaddition of three of its anthracene lig
112 particles as solid, recyclable catalysts for Diels-Alder cycloadditions of 2'-hydroxychalcones and di
113 ynamically determined product selectivity in Diels-Alder cycloadditions of 3-methoxycarbonylcyclopent
115 egy involves highly stereocontrolled [4 + 2] Diels-Alder cycloadditions of chiral, nonracemic epoxyqu
117 with two ester substituents were prepared by Diels-Alder cycloadditions of cyclopentadiene with dimet
119 elopment of the base-mediated intramolecular Diels-Alder cycloadditions of tryptamine-derived Zincke
120 ediates subsequently undergo either a formal Diels-Alder cycloaddition or a competitive Michael addit
122 ioselectivity of different reactions such as Diels-Alder cycloadditions or Bingel-Hirsch reactions.
125 ed anthracene-based monomer for topochemical Diels-Alder cycloaddition polymerization crystallized wi
126 ganic polymer (3D p-POP) using catalyst-free Diels-Alder cycloaddition polymerization followed by aci
127 An improved procedure for the intramolecular Diels-Alder cycloaddition previously reported in our syn
129 several nonbiological reactions, including a Diels-Alder cycloaddition, proton transfer, multistep re
130 yclobutenone was employed as a dienophile in Diels-Alder cycloadditions, provide diverse and complex
131 nones has been achieved by an intramolecular Diels--Alder cycloaddition reaction (IMDAF) of furanyl c
134 ing advantage of the decarbonylative [4 + 2] Diels-Alder cycloaddition reaction between ethynyl and t
135 d from the three-step sequence involving the Diels-Alder cycloaddition reaction can be employed as ad
137 nes 6a-f, respectively, which were used in a Diels-Alder cycloaddition reaction in the synthesis of t
139 actions on-water, is a regioselective hetero-Diels-Alder cycloaddition reaction of enol ethers to 4-p
140 abicyclo[6.2.1]-5-undecen-9-one; and (iii) a Diels-Alder cycloaddition reaction to construct the thir
141 talline arrangement for their intermolecular Diels-Alder cycloaddition reaction to form a linear poly
147 of an optical cavity to modulate the rate of Diels-Alder cycloaddition reactions and to achieve stere
149 lysis and selectivity in Lewis acid-promoted Diels-Alder cycloaddition reactions involving vinylazaar
151 ontrol of an optical cavity for two selected Diels-Alder cycloaddition reactions using the quantum el
154 bon templates, without metal catalysis, by a Diels-Alder cycloaddition/rearomatization strategy, usin
155 as achieved via an intramolecular amidofuran Diels-Alder cycloaddition/rearrangement followed by an i
156 the four possible reaction pathways for the Diels-Alder cycloaddition (relative approach of the dien
158 and strain-promoted inverse electron-demand Diels-Alder cycloaddition (SPIEDAC) targeted to cyclopro
159 arrangement suitable for their topochemical Diels-Alder cycloaddition (TDAC) to form a linear polyme
160 ly specific, stereoconvergent intramolecular Diels-Alder cycloaddition that led to the trans-decalin
162 the strain-promoted inverse electron-demand Diels-Alder cycloaddition, that is, tetrazine ligation,
163 transfer of stereochemical information in a Diels-Alder cycloaddition through a point-chirality, axi
164 fic functional end group, by means of hetero-Diels-Alder cycloaddition through their inherent termina
165 cloadditions--the homologous Diels-Alder and Diels-Alder cycloadditions--through a vinylogous Peterso
167 The utility of this monomer in the [4 + 2] Diels-Alder cycloaddition to produce well-defined, sulfo
168 bottlebrush networks using thermoreversible Diels-Alder cycloadditions to enable both reversible dis
169 mercially available arylsulfonyl cyanides in Diels-Alder cycloadditions to generate isopyridine cyclo
170 ovel strategy harnesses the high-fidelity of Diels-Alder cycloadditions to quickly construct multi-su
171 absolute stereochemistry in the acylnitroso Diels-Alder cycloaddition took advantage of an activated
172 by way of a stereocontrolled intramolecular Diels-Alder cycloaddition via adoption of an endo transi
173 As a key-step, a chiral auxiliary-mediated Diels-Alder cycloaddition was developed, introducing the
176 ein, featuring an unprecedented oxopyrrolium Diels-Alder cycloaddition which furnishes a key tetracyc
177 n bonds and up to four stereo-centres is the Diels-Alder cycloaddition, which occurs between a 1,3-bu
178 r the CtdP-catalysed inverse electron demand Diels-Alder cycloaddition, which serves as the first exa
179 l)-1,3-butadiene (9) in situ which underwent Diels--Alder cycloaddition with various dienophiles to f
180 nder mild conditions and intercepted through Diels-Alder cycloaddition with a diene trapping agent.
181 s, iminium precursor 22a underwent efficient Diels-Alder cycloaddition with a range of simple and com
182 abeled with (18)F by inverse electron demand Diels-Alder cycloaddition with a trans-cyclooctene attac
183 he competition between self-dimerization and Diels-Alder cycloaddition with an external dienophile us
184 (Z)-alpha-fluoroenaminophosphonates, whereas Diels-Alder cycloaddition with cyclopentadiene provides
186 4-Chloro-2(H)-pyran-2-one undergoes thermal Diels-Alder cycloaddition with electron-deficient dienop
187 n, some of these compounds underwent [4 + 2] Diels-Alder cycloaddition with electron-deficient dienop
189 2H-pyran nucleus was evaluated as a diene in Diels-Alder cycloaddition with reactive dienophiles.
190 gged protein through inverse electron demand Diels-Alder cycloaddition with subsequent double retro-D
191 P) and retains its reactivity for subsequent Diels-Alder cycloaddition with the in situ generated ben
193 o dienyl sulfoxides undergo highly selective Diels-Alder cycloadditions with N-phenylmaleimide with r