3
Early Research: Separation of Optically Active Styrenes
In 1930, the attempt of Maxwell and Adams[4 ] to separate the enantiomers of styrenes 2 , 3 , and 4 by resolution ended with failure (Scheme [1 ]), with the low steric bulk of the α-hydrogen atom of the styrene accounting for the unaccomplished separation. In 1938, Mills and Dazeley[5 ] succeeded in synthesizing racemic o -(β,β-dimethyl-α-isopropylvinyl)-phenyltrimethyl ammonium iodide (5 ) and resolving its isomers, which verified the original postulate about the possibility of stable atropisomerim in styrenes. On replacing the methyl group (with Z -geometry to the aryl ring) with a hydrogen atom to form 6 , no enantiomers could be separated.
Scheme 1 Atropisomeric styrenes in early studies
In 1940, Miller and Adams[6 ] completed the synthesis of a more sterically hindered styrene, β-chloro-β-(2,4,6-trimethyl-3-bromophenyl)-α-methylacrylic acid (7 ), and its enantiomers were successfully resolved. With a chlorine atom at the β-position of the styrene and a methyl group adjacent to the axis, compound 7 demonstrated excellent stability, displaying no decrease in enantiopurity on heating to reflux in ethanol for 15 h or in glacial acetic acid for 12 h. Bromination of 7 afforded the optically inactive symmetric compound 8 . In contrast, the installation of a sulfonyl group on 7 gave the optically active compound 9 . Later, Adams and co-workers carried out further research into the relevance between structure and atropisomeric stability in styrenes.[6 ]
[7 ]
Notable retention of partial chirality was observed by Fuji and co-workers in the alkylation reaction of 10 with a carbon stereogenic center at the α-position of a carbonyl group in 1991.[8 ] It seemed that the size of the electrophile did not affect the enantioselectivity (Scheme [2 ], table). The authors carried out rapid HPLC analysis of byproduct 12 , which gave a 65% enantiomeric excess (ee) value. The control experiment indicated that alkylation would form atropisomeric enolate INT-1 , which could be attacked by the electrophile to afford the C-alkylation product 11 and O-alkylation product 12 with moderate ee values (Scheme [2 ], bottom).
Scheme 2 Enantioselective alkylation via an intermediate atropisoenolate
In 2016, Clayden and co-workers[9 ] synthesized a series of 1-aryl-3,4-dihydroisoquinolines 13 , which are structural analogs of styrene featuring a potentially atropoisomerically stable axis. They studied the stabilities by calculation of the rotational barrier energies. The data given in Figure [1 ] show that the stability increased as the size of the adjacent substituted moiety X increased (13a –13f ). Nevertheless, the half-life of iodide 13d was too short to separate the enantiomers at ambient temperature.
Figure 1 Substituent effect on the stability of 1-aryl-3,4-dihydroisoquinolines
4
Synthesis of Optically Active Styrenes
Given the unique scaffolds of atropisomeric styrenes and their important applications in bioactive molecules and medicines, many approaches to access enantioselective styrenes have been developed during recent decades. In early studies, atropisomeric chirality was constructed from point chirality via chirality transfer. The optically active styrenes could be separated as single distereomers with the aid of chiral auxiliaries. Of all approaches, catalytic asymmetric synthesis comes to the fore because of its high efficiency and divergent functional-group tolerance. Recently, transition-metal-catalyzed cross-couplings, including C–H functionalization in a step- and atom-economic manner, have become a powerful method for the preparation of atropoactive styrenes. Furthermore, organo-catalyzed electrophilic addition of vinylidene ortho -quinone methide type intermediates is also an attractive approach.
4.1
Chirality Transfer Strategy
In 2001, Miyano, Hattori, and co-workers[10 ] reported the synthesis of tertiary alcohol (R ,R )-16 , which was derived from the 1,2-addition of (R )-14 and 15 . Compound 16 was stereospecifically transformed into atropisomeric (R )-17 with up to 95% ee on treatment with (CF3 CO)2 O in dichloromethane at room temperature (Scheme [3 ]). Interestingly, the authors found that there was an equilibrium between conformational isomers 16a and 16b observable from the 1 H NMR spectrum. The ratio was 1:5.7 in CDCl3 but ranged from 1:1 to 1:6.3 depending on the solvent. The chirality transfer from point to axial chirality can be assumed to occur because of the much lower conversion rate from 16a into (R )-17 than the rate from 16b into (S )-17 .
Scheme 3 Synthesis of atroposelective styrenes via chirality transfer
4.2
Chiral Auxiliary Strategy
With the assistance of chiral auxiliaries, chiral atropisomeric styrenes can be synthesized in a diastereoselective manner. Subsequent removal of the auxiliary affords the atropisomeric styrenes. In 1996, Baker et al.[11 ] disclosed a point to axial chirality transfer via a formal 1,3-hydrogen shift (Scheme [4 ]). Reaction of (1R )-menthyl (R )-(1-p -tolylsulfinyl)-naphthalene-2-carboxylate (18 ) with indenyllithium delivered major product 19 in 88% yield and with 59% diastereoselectivity, together with minor products 20 and 21 in a combined yield of 9% with a ratio of 1:1. Esters 20 and 21 , with relatively stable axial chirality, were separated by preparative HPLC. The half-life of interconversion between 20 and 21 was about 25 h in solution at 25 °C. Treatment of isomer 19a (99% de) with an excess of LiAlH4 afforded carbinol ent -22 in quantitative yield with 98% ee. A control experiment was performed by quenching the reaction with DCl in D2 O within 5 mins and gave ent -22 with 89% deuterium incorporation. The authors proposed that the reduction of 19a with the S -conformation at C-1′ gave ent -22 -d via INT-2 , on the basis of this labeling experiment.
Scheme 4 Point to axial chirality transfer strategy
Diastereoselective synthesis of axial styrenes with the aid of a chiral sulfoxide auxiliary was applied successfully to the stereospecific synthesis of the antibiotic TAN-1085 (23 ). Suzuki and co-workers[12 ] reported an asymmetric synthesis of 23 through a stereochemical relay strategy featuring a three-step conversion of chirality: central to axial (step A), axial to axial (step B), and axial to central (step C) (Scheme [5 ]). Suzuki–Miyaura coupling of boronic acid 24 and vinyl iodide 25 containing the chiral sulfoxide auxiliary and subsequent silylation and mono-deprotection of the phenol afforded atropisomeric styrenes 27a and 27b with a diastereoselective ratio of 25:75. Conformation 27b was favored over 27a by the formation of an intramolecular hydrogen bond. Product 27b was separated by flash chromatography on silica gel, and subsequent benzylation gave 28 in more than 99% ee, which could be enantioselectively converted into TAN-1085 in a few steps.
Scheme 5 Asymmetric synthesis of TAN -1085 (23 )
Scheme 6 Synthesis of atropisomeric styrenes with a chiral sulfide auxiliary
Meanwhile, the same group[13 ] realized an asymmetric synthesis of atropisomeric styrenes bearing two axial axes via a similar strategy (Scheme [6 ]). Treatment of vinyl iodide 30 , featuring a chiral sulfoxide auxiliary, with aryl boric acid 29 furnished atropisomeric styrene 31 as one diastereomer. After a two-step transformation, 32 , bearing two terminal alkenes, was prepared from 31 and could be selectively converted into planar chiral cyclophane 33 . In a similar procedure, planar chiral cyclophanes 34 and 35 , also with the ansa -chain, were readily accessed. The atropisomeric vinyl arene structure also possibly exists in ring-strained macrobiaryl alkenes.[14 ]
4.3
Catalytic Asymmetric Synthesis of Atropisomeric Styrenes
Benefiting from the rapid development of transition-metal-catalyzed cross-coupling reactions, many novel and efficient approaches to access atropisomeric styrenes have been developed. These strategies include the cross-coupling of aryl halides and hydrazones, Suzuki–Miyaura cross-couplings, and cross--coupling reactions via C–H activation.
It is anticipated that, when styrene structures have the vinyl unit as part of a five- or six-membered ring fused to another aromatic ring, the atropisomerism of these compounds may be more stable than that of acyclic styrenes. For example, dihydro-binaphthalenes and 1-(1H -inden-3-yl)naphthalene are supposed to have higher rotational barriers than vinyl naphthalenes.
Scheme 7 Carbene strategy for the synthesis of atropisomeric styrenes
4.3.1
Palladium-Catalyzed Cross-Coupling of Aryl Halides And Hydrazones
In view of the importance of the axial chirality in styrenes, in 2016, Gu and co-workers[15 ] developed the first catalytic asymmetric synthesis of styrene-type atropisomers (Scheme [7 ]). The protocol with aryl halides 36 and hydrazones 37 as standard substrates delivered dihydro-binaphthalenes 38 in up to 99% yield with up to 97% ee. The reaction exhibited a broad functional-group tolerance. In the proposed mechanism, the oxidative insertion of Pd(0) into 36 gives INT-3 , which coordinates with the in situ generated carbene species derived from hydrazone 37 with the aid of t BuOLi. The newly formed palladium carbene species INT-4 undergoes migration/insertion reactions to produce INT-5 , which affords the final product via reductive elimination and liberation of the Pd(0) catalyst. The chiral styrene was readily oxidized to the atropisomeric biaryl compound without erosion of enantiopurity. Moreover, the P(V) compound 38a was uneventfully reduced to phosphine 40 , which was successfully applied in an asymmetric allylation reaction as an (alkene, phosphine) bidentate ligand.
In further related studies, Wu et al.[16 ] employed P-stereogenic bidentate phosphine ligand 44 in the asymmetric synthesis of atropisomeric vinyl arenes with excellent stereocontrol (Scheme [8 ]). In this report, dialkyl phosphonates 41 were compatible substrates, delivering atropisomeric vinyl arenes 43 with good yields and enantioselectivities. The protocol was successfully applied to the synthesis of atropisomeric compound 43b containing an indene skeleton (86% ee). For product 43c , with a seven-membered ring, the racemic product was observed. Diphenyl phosphine oxide 38a was synthesized in 75% yield with 87% ee, which is slightly lower than the results of Gu and co-workers. The utility was demonstrated by a gram-scale synthesis of 43e without loss of enantioselectivity. The merit of this work is that dimethyl phosphonate 43a could be further converted into dimethyl phosphine oxide 45 with methyl magnesium bromide.
Scheme 8 Palladium-catalyzed atropisomeric styrene synthesis with aryl halides and carbene precursors
4.3.2
Suzuki–Miyaura Cross-Coupling for Synthesis of 2-Aryl Cyclohex-2-Enone Atropisomers
In 2017, Gu and co-workers[17 ] disclosed an asymmetric synthesis of 2-aryl cyclohex-2-enone atropisomers 48 via Suzuki–Miyaura coupling of 2-iodo-3-methylcyclohex-2-enones 46 and aryl boronic acids (Scheme [9 ]). BoPhoz 49 exhibited superior stereocontrol over other types of ligand. The advantage of this strategy is that the α,β-unsaturated ketone displays diverse reactivity in its downstream transformations. Thus, the final products bearing axial chirality, known as ‘platform molecules,’ could be diversely converted into atropisomeric biaryls. For example, 48a was oxidized into quinone 50 with TBHP in presence of [Co(acac)2 ]. Furthermore, 48a underwent aromatization with NBS and a catalytic amount of BPO to deliver phenol 51 , without loss of axial integrity. After a three-step transformation, involving oxime formation, reduction, and aromatization, α-amino atropisomeric biaryl 52 was prepared efficiently. A benzyl group could be installed at the β-position in 53 by an aldol reaction followed by oxidation. Notably, aryl iodide 54 could also be accessed in 75% yield over three steps via condensation with hydrazide followed by iodization and aromatization.
Scheme 9 Divergent syntheses from atropisomeric styrenes
4.3.4
C–H Activation for the Synthesis of Atroposelective Vinyl Arenes
The last twenty years have witnessed important developments in C–H activation strategies in organic synthesis.[1c ]
[18 ] Several approaches based on C–H activation have been developed for the construction of atropisomeric styrenes.
In 2018, Gu and co-workers[19 ] developed a visible-light-accelerated stereospecific C–H arylation for the preparation of tetrasubstituted atropisomeric vinyl arenes. The reaction was based on their previously synthesized atropisomeric vinyl arene 38 , which reacted with diaryliodonium salts to give 56 without loss of enantiopurity (Scheme [10 ]). A radical pathway was proposed on the basis of control experiments and DFT calculations. A diaryl iodine cation can be formed from diaryliodonium salts under standard conditions, which can lead to iodobenzene cationic radical INT-6 and phenyl radical INT-7 under irradiation. Radical addition to 38 , followed by association with the palladium catalyst and β-H elimination give the final product. Kinetic studies showed that the kinetic isotope effect value changed from 3.6 in the absence of light to 1.1 on irradiation with visible light, which indicated that the C–H functionalization step was the rate-determining step in the absence of irradiation with visible light.
Scheme 10 Visible-light-mediated C–H arylation
Based on the α-aryl-α,β-cyclohexenone skeleton, Cui, Xu, and co-workers[20 ] reported an asymmetric oxime-directed C–H olefination reaction in 2018 (Scheme [11 ]). Under Pd(OAc)2 catalysis, Ac-l -Ala-OH and 2-aryl cyclohex-2-enone oxime ethers 57 were smoothly converted into atropisomeric vinyl arenes 58 with excellent enantioselectivity. One of the two C–C double bonds in 58a could be selectively reduced to give 59 via Pd/C catalysis under an atmosphere of hydrogen. After acting as a temporary directing group, the oxime ether group could be removed to release the ketone group with HCl. Diaryl phosphine 61 was achieved by treating 58b with diphenyl phosphorus chloride; the product was subjected to asymmetric allylation to provide 62 in moderate yield with 37% ee.
Scheme 11 Palladium-catalyzed C–H olefination with oxime ether as a directing group
In 2019, Liu, Mao, and co-workers[21 ] developed a carbopalladation and C–H olefination for the asymmetric synthesis of atropisomeric styrenes (Scheme [12 ]). Treatment of alkyne 63 with naphthyl iodide 64 afforded atropoactive styrene 65 featuring an oxindole scaffold with moderate enantioselectivity. In this reaction, the TADDOL-derived phosphoramidite ligand 66 displayed the best stereoinduction. A mechanism involving intramolecular C–H activation was proposed. The atroposelective insertion of the C≡C triple bond of 63 into INT-12 gave INT-13 , which was regarded as the key intermediate for stereoinduction. An intramolecular C–H palladation of INT-13 formed palladacycle INT-14 , which delivered final product 65 and liberated Pd(0) after reductive elimination.
Scheme 12 Double functionalization of an alkyne
By using the concept of transient chiral auxiliaries, Shi and co-workers[22 ] realized a palladium-catalyzed asymmetric olefination of styrene 67 in 2020 (Scheme [13 ]). Chiral amino amide 70 was chosen as the optical transient chiral auxiliary, and atropisomeric styrenes 69 were synthesized with good yields and high stereoselectivity (up to 99% ee). Palladacycle complex 72 was prepared by treating 71 , featuring an imine moiety, with stoichiometric Pd(OAc)2 in 35% yield. The structure of palladium complex 72 was confirmed by single-crystal X-ray diffraction analysis. The application of 72 instead of Pd(OAc)2 /70 to the asymmetric C–H olefination reaction under the standard conditions gave optically active 69a with 80% ee, which indicated the possibility of an in situ formed amino amide transient directing group. The utility of the products was demonstrated by employing the corresponding α,β-unsaturated chiral carboxylic acids (CCAs) as chiral ligands for the enantioselective Csp3 –H amidation of thioamides. In comparison with biaryl acid 75 , the styrene-based acid 74 derived from 69 gave an improved enantioselectivity (from 42% ee to 64% ee).
Scheme 13 C–H olefination strategy
Later, the same group[23 ] disclosed the asymmetric synthesis of atropisomeric styrenes via C–H alkenylation by using a 2-pyridyl moiety as a directing group (Scheme [14 ]). The starting material 76 could ‘freely’ rotate around the vinyl–arene axis under the reaction conditions. The pyridine nitrogen atom could coordinate with palladium and the readily available l -pyroglutamic acid to form INT-15 . Through good cooperation of the directing group and chiral ligand, modulation of the reactivity and induction of the stereoselectivity were achieved to give atropisomeric products 77 with good yields and enantioselectivity. The generality of substrate scope was investigated with different substituted styrenes. The reaction with alkynyl bromide was also successful, giving the coupling products with very high enantiopurity.
Scheme 14 Pyridine-group-directed asymmetric C–H functionalization
Very recently, Wang and co-workers[24 ] reported a C–H olefination and arylation for the asymmetric synthesis of atropisomeric styrenes by utilizing a carboxylic acid direction strategy (Scheme [15 ]). The protocol demonstrated a broad substrate scope, high yields, and excellent stereoselectivity (up to 99% ee). Notably, the absolute configuration of the products was the opposite configuration to the products of Shi and co-workers, despite Boc-l -leucine and 70 being derived from the same amino acid, l -leucine. The authors explained these observations by proposing two different models for the stereoinduction. In TS-1 , the bulky alkyl chain of the amino acid points upward and pushes the alkenyl group away from the palladium. However, in TS-2 , the upward t Bu group forces the alkenyl group downward, which leads to the opposite configuration. The utility of these CCAs was further demonstrated by two Cp*Co(CH3 CN)3 [SbF6 ]2 /CCA-catalyzed asymmetric C–H functionalization reactions.
Scheme 15 Asymmetric C–H olefination and arylation with a carboxylic acid directing group
4.4
Atropisomeric Synthesis of Styrenes Prompted by Nucleophilic Addition
In 2017, Tan and co-workers[25 ] reported an organocatalyzed atroposelective synthesis of atropisomeric styrenes by means of nucleophilic addition to propanal derivatives (Scheme [16 ]). In the presence of chiral pyrrole 83 , alkynal 81 was activated by forming INT-16 , which underwent nucleophilic attack to generate INT-17 stereoselectively. Isomerization of INT-17 gave iminium ion INT-18 , which could be converted into final product 82 by hydrolysis. With regard to substrate scope, styrenes bearing an iodine and sulfophenyl group (82a , 82b ) could be tolerated, but installation of a methyl group at the α-position of the axis greatly decreased the stereoselectivity to 54% ee (82c ). A nucleophile containing an allyl moiety was also compatible (82d ).
Scheme 16 Chiral pyrrole-catalyzed synthesis of chiral styrenes
In 2018, Yan and co-workers[26 ] described an enantioselective synthesis of sulfone-containing atropisomeric styrenes with the cooperation of quinine-derived thiourea 86 and l -proline (Scheme [17 ]). A series of enantioenriched styrenes 85 was prepared with good enantioselectivity and excellent E /Z selectivity by treating 1-alkynyl-naphthalen-2-ols 84 with sodium sulfinates. Based on control experiments and DFT calculations, a vinylidene o -quinone methide (VQM) was proposed as the key intermediate, which significantly influenced the subsequent series of studies in this area. VQM intermediate INT-19 bears an atropisomeric allenyl moiety, which is critical for the high enantioselectivity in subsequent reactions. The activated sulfinate anion derived from the combination of l -proline and sodium sulfinate would act as a nucleophile to attack INT-19 , forming final product 85a . The role of boric acid was probably to release l -proline from the complex for the next catalytic cycle.
Scheme 17 Synthesis of atropisomeric styrenes via VQMs
Based on the key optically active intermediate, VQM, Yan and co-workers[27 ] completed the asymmetric synthesis of atropisomeric sulfone-containing styrenes bearing up to three axes with high enantio- and diastereoselectivities (Scheme [18a ]). Alkynes 87 reacted with arylsulfinic acid to deliver enantioenriched multi-axis styrenes 88 smoothly with the assistance of the chiral quinine-derived squaramide catalysts 89 via tetrasubstituted VQM INT-20 . This allowed kinetic resolution with an excellent selectivity factor (S ). Later, the same group[28 ] disclosed the asymmetric synthesis of atropisomeric 1,4-distyrene 2,3-naphthalene diols by means of organocatalysis (Scheme [18b ]). Nucleophilic addition of an amidosulfone to a VQM with the aid of cinchona squaramide 93 under mild reaction conditions afforded 92 featuring two chiral axes. Catalytic asymmetric synthesis of a sulfone-containing atropisomeric styrene via the Michael addition reaction of α-amido sulfones to ynones was achieved by the same group (Scheme [18c ]).[29 ] The methodology employed N -squaramide 96 as the catalyst, giving the atropisomeric styrenes 95 with excellent enantioselectivity.
Scheme 18 Synthesis of atropisomeric styrenes via tetrasubstituted VQMs
Benefiting from the versatile reactivity of VQM and its analogs, in 2019, Tan and co-workers[30 ] achieved the construction of a series of disubstituted atropisomeric 1,1′-(ethene-1,1-diyl)binaphthol (EBINOL) derivatives by utilizing 2-naphthol as the nucleophile (Scheme [19 ]). Under catalysis with compound 100 , atropisomeric styrenes 99 were synthesized in high yields and enantioselectivity, along with complete E /Z selectivity, under mild reaction conditions. The utility of this transformation was exhibited by the preparation of atropisomeric EBINOL-based chiral phosphonic acid (ECPA) 101 and phosphoramidites 105a and 105b . Under catalysis with 101 , alkylation of indole (102 ) with N -(1-phenylvinyl)acetamide (103 ) afforded tertiary amine 104 smoothly with moderate enantioselectivity. By contrast, a BINOL-derived CPA gave a lower stereoselectivity and a SPINOL-based CPA failed in the induction of enantioselectivity. The phosphoramidite was obtained as the pair of diastereoisomers 105a and 105b exhibiting P-stereocenters because of the lack of C2 -symmetry of EBINOL. EBINOL-Phos 105a efficiently prompted the asymmetric hydrogenation of enamides 106 with 97% yield and 90% ee, whereas 105b afforded the product in low yield. The alternative phosphoramidites Phos-bs and Phos-sr did not give satisfactory results.
Scheme 19 Atroposelective synthesis of atropisomeric EBINOL
In 2020, Li, Yan, Liu, and co-workers[31 ] applied asymmetric nucleophilic addition for the synthesis of atropisomeric styrenes bearing a stereocenter and a chiral axis (Scheme [20 ]). Racemic 5H -oxazol-4-ones 109 worked as nucleophiles to attack the in situ formed VQM intermediate derived from 108 to afford 110 with high enantioselectivity, high diastereoselectivity, and a good E /Z ratio. This method offers an efficient approach to these stereoisomers, which have potential applications in asymmetric synthesis.
Scheme 20 Construction of atropisomeric styrenes with multiple stereoelements
N-Alkylation of enamide 112 also enabled preparation of atropisomeric styrenes.[32 ] Nucleophilic substitution of alkyl bromides with 112 in the presence of a catalytic amount of 114 afforded enantioenriched styrenes 113 with satisfactory stereoselectivity and good functional-group tolerance (Scheme [21 ]). Substrates including allyl bromide, propargyl bromide, 4-methoxybenzyl bromide, and benzyl bromide were successfully applied in the protocol (113a –113e ). A merit of this methodology was the rapid preparation of atropisomeric 2-arylpyrrole scaffold 115 by treating 113e with LDA. Atropisomer 116 , featuring a seven-membered cyclic system, was also prepared by reduction of 113a with DIBAL-H followed by annulation with good enantioselectivity and 78:22 diastereoselectivity.
Scheme 21 Synthesis of atropisomeric styrenes via N-alkylation
Scheme 22 Synthesis of atropisomeric styrenes via an aza-VQM intermediate
In 2020, Zhao and co-workers[33 ] identified an aza-VQM as a key intermediate for the preparation of atropisomeric vinyl α-anilines. A well-defined chiral sulfide was used as the catalyst, which promoted an asymmetric electrophilic carbothiolation and intramolecular annulation reaction (Scheme [22 ]). INT-20 was formed by coordination of sulfur reagent 118 and catalyst 120 with the aid of a Lewis acid. Subsequently, INT-20 reacted with alkyne 117 to generate sulfonium salt INT-21 , which transformed into aza-VQM INT-22 by elimination and liberated the catalyst. Intramolecular annulation of INT-22 afforded sulfur-containing atropisomeric styrenes 119 .
Following this, Zhang and co-workers[34 ] reported an asymmetric nucleophilic addition of 1-(ethynyl)naphthalen-2-amines to achieve a divergent synthesis of atropisomeric styrenes (Scheme [23 ]). The reaction employed indoles or 4-hydroxycoumarins as substrates, and high yields and excellent enantioselectivity were obtained. Based on previous work and control experiments, a mechanism involving a π–π interaction and hydrogen-bond-mediated model was proposed. Combination of 121a with chiral phosphoric acid 124 would generate INT-23 , which could isomerize to aza-VQM INT-24 in an enantioselective form. INT-24 could then be attacked by the indole to give INT-26 . Subsequent dissociation of INT-26 would afford enantioenriched 122a and regenerate 124 . The hydrogen bond plays a vital role in the reactivity and enantiocontrol. By contrast, N -methyl indole displayed no selectivity under identical conditions.
Scheme 23 Chiral phosphoric acid catalyzed atroposelective synthesis of styrenes
An atropisomeric styrene framework bearing a novel seven-membered bridged ring was also synthesized by Shi and co-workers in 2020 (Scheme [24 ]).[35 ] (3-Alkynyl-2-indolyl)methanols 125 can readily generate optically active allenes with the assistance of chiral phosphorous acid 127 , which was atroposelectively attacked by 2-naphthol to give acyclic chiral styrenes. Intramolecular dehydration afforded the fused atropisomeric styrene 126 .
Scheme 24 Atropisomeric styrene synthesis from 3-alkynyl-2-indolylmethanols
Later, the same group[36 ] reported a kinetic resolution of indole-based vinyl aniline 128 (Scheme [25 ]). The resolution, featuring a high selectivity factor (S ), allowed efficient control of conversion and enantioselectivity and offered an approach to a new class of atropisomeric styrenes.
Scheme 25 Catalytic kinetic resolution
4.5
Asymmetric Phase-Transfer Alkylation
Enolization of 3,4-dihydronaphthalen-2(1H )-one gives a 3,4-dihydronaphthalen-2-ol intermediate. In 2017, Smith and co-workers[37 ] realized an asymmetric O -alkylation strategy for the atroposelective synthesis of atropisomeric styrenes via chiral phase-transfer catalysis (Scheme [26 ]). The methodology employed ketone 132 as the enolate precursor. O-Alkylation with the assistance of chiral ammonium salt 134 afforded enol ether 133 with excellent enantioselectivity. The procedure commenced with racemic ketone 132 , featuring central chirality, as the substrate; this could generate the enolate with the aid of solid potassium phosphate and coordinate with the chiral ammonium salt to afford soluble diastereoselective ion pairs INT-27 and INT-28 . The diastereomers bearing atropisomeric information could interconvert through protonation and deprotonation. Atropisomeric styrene 133a was exposed to m -chloroperoxybenzoic acid to afford the corresponding epoxide, which was subsequently rearranged with catalytic ytterbium triflate to give 135 with central chirality. BINOL 136 was obtained readily by oxidation and dealkylation of 133a without erosion of enantioselectivity.
Scheme 26 Asymmetric O-alkylation
