Exploiting the Multidentate Nature of Chiral Disulfonimides in a Multicomponent Reaction for the Asymmetric Synthesis of Pyrrolo[1,2‐a]indoles: A Remarkable Case of Enantioinversion

A new multicomponent coupling reaction for the enantioselective synthesis of pyrrolo[1,2‐a]indoles under the catalysis of a chiral disulfonimide is described. The high specificity of the reaction is a consequence of the multidentate character of the Brønsted acid catalyst. Insights from DFT calculations helped explain the unexpected high enantioselectivity observed with the simplest 3,3′‐unsubstituted binaphthyl catalyst as a result of transition‐state stabilization by a network of cooperative noncovalent interactions. The remarkable enantioinversion resulting from the simple introduction of substituents at 3‐ and 3′‐positions, the first reported example of this phenomenon in the context of binaphthalene‐derived Brønsted acid catalysis, was instead attributed to destabilizing steric interactions.     

Methylene‐Bridged Metallocenes with 2,2′‐Methylenebis[1H‐inden‐1‐yl] Ligands: Synthesis,Characterization, and Polymerization Catalysis of a Synthetically Simple Class of C2‐ and C2v‐Symmetric ansa‐Metallocenes

The acid‐catalyzed reaction between formaldehyde and 1H‐indene, 3‐alkyl‐ and 3‐aryl‐1H‐indenes, and six‐membered‐ring substituted 1H‐indenes, with the 1H‐indene/CH₂O ratio of 2 : 1, at temperatures above 60° in hydrocarbon solvents, yields 2,2′‐methylenebis[1H‐indenes] 1 – 8 in 50–100% yield. These 2,2′‐methylenebis[1H‐indenes] are easily deprotonated by 2 equiv. of BuLi or MeLi to yield the corresponding dilithium salts, which are efficiently converted into ansa‐metallocenes of Zr and Hf. The unsubstituted dichloro{(1,1′,2,2′,3,3′,3a,3′a,7a,7′a‐η)‐2,2′‐methylenebis[1H‐inden‐1‐yl]}zirconium ([ZrCl₂( 1′ )]) is the least soluble in organic solvents. Substitution of the 1H‐indenyl moieties by hydrocarbyl substituents increases the hydrocarbon solubility of the complexes, and the presence of a substituent larger than a Me group at the 1,1′ positions of the ligand imparts a high diastereoselectivity to the metallation step, since only the racemic isomers are obtained. Methylene‐bridged ‘ansa‐zirconocenes’ show a noticeable open arrangement of the bis[1H‐inden‐1‐yl] moiety, as measured by the angle between the planes defined by the two π‐ligands (the ‘bite angle’). In particular, of the ‘zirconocenes’ structurally characterized so far, the dichloro{(1,1′,2,2′,3,3′,3a,3′a,7a,7′a‐η)‐2,2′‐methylenebis[4,7‐dimethyl‐1H‐inden‐1‐yl]}zirconium ([ZrCl₂( 5′ )] is the most open. The mixture [ZrCl₂( 1′ )]/methylalumoxane (MAO) is inactive in the polymerization of both ethylene and propylene, while the metallocenes with substituted indenyl ligands polymerize propylene to atactic polypropylene of a molecular mass that depends on the size of the alkyl or aryl groups at the 1,1′ positions of the ligand. Ethene is polymerized by rac‐dichloro{(1,1′,2,2′,3,3′,3a,3′a,7a,7′a‐η)‐2,2′‐methylenebis[1‐methyl‐1H‐inden‐1‐yl]}zirconium ([ZrCl₂( 2′ )])/MAO to polyethylene waxes (average degree of polymerization ca. 100), which are terminated almost exclusively by ethenyl end groups. Polyethylene with a high molecular mass could be obtained by increasing the size of the 1‐alkyl substituent.     

A New Class of Tunable Dendritic Diphosphine Ligands: Synthesis and Applications in the Ru‐Catalyzed Asymmetric Hydrogenation of Functionalized Ketones

A series of tunable G₀–G₃ dendritic 2,2′‐bis(diphenylphosphino)‐1,1′‐binaphthyl (BINAP) ligands was prepared by attaching polyaryl ether dendrons onto the four phenyl rings on the P atoms. Their ruthenium complexes were employed in the asymmetric hydrogenation of β‐ketoesters, α‐ketoesters, and α‐ketoamides to reveal the effects of dendron size on the catalytic properties. The second‐ and third‐generation catalysts exhibited excellent enantioselectivities, which are remarkably higher than those obtained from the small molecular catalysts and the first‐generation catalyst. Molecular modeling indicates that the incorporation of bulky dendritic wedges can influence the steric environments around the metal center. In addition, the ruthenium catalyst bearing a second‐generation dendritic ligand could be recycled and reused seven times without any obvious decrease in enantioselectivity.     

Double Stereodifferentiation in the Catalytic Asymmetric Aziridination of Imines Prepared from α‐Chiral Amines

The catalytic asymmetric aziridination of imines and diazo compounds (AZ reaction) mediated by boroxinate catalysts derived from the VANOL and VAPOL ligands was investigated with chiral imines derived from five different chiral, disubstituted, methyl amines. The strongest matched and mismatched reactions with the two enantiomers of the catalyst were noted with disubstituted methyl amines that had one aromatic and one aliphatic substituent. The synthetic scope for the AZ reaction was examined in detail for α‐methylbenzyl amine for cis‐aziridines from α‐diazo esters and for trans‐aziridines from α‐diazo acetamides. Optically pure aziridines could be routinely obtained in good yields and with high diastereoselectivity and the minor diastereomer (if any) could be easily separated. The matched case for cis‐aziridines involved the (R)‐amine with the (S)‐ligand, but curiously, for trans‐aziridines the matched case involved the (R)‐amine with the (R)‐ligand for imines derived from benzaldehyde and n‐butanal, and the (R)‐amine with the (S)‐ligand for imines derived from the bulkier aliphatic aldehydes pivaldehyde and cyclohexane carboxaldehyde.     

Design of Binaphthyl‐Modified Symmetrical Chiral Phase‐Transfer Catalysts: Substituent Effect of 4,4′,6,6′‐Positions of Binaphthyl Rings in the Asymmetric Alkylation of a Glycine Derivative

A series of symmetrical chiral phase‐transfer catalysts with 4,4′,6,6′‐tetrasubstituted binaphthyl units have been designed, and these aryl‐ and trialkylsilyl‐substituted phase‐transfer catalysts, which included a highly fluorinated catalyst, were prepared. The chiral efficiency of these chiral phase‐transfer catalysts was investigated in the asymmetric alkylation of tert‐butylglycinate–benzophenone Schiff base under mild phase‐transfer conditions, and the eminent substituent effect of the 4,4′,6,6′‐positions of the binaphthyl units on enantioselection was observed. In particular, the OctMe₂Si‐substituted catalyst was found to be highly efficient for the phase‐transfer alkylation of tert‐butylglycinate–benzophenone Schiff base with various alkyl halides, including sec‐alkyl halides. The highly fluorinated catalyst was also utilized as a recyclable chiral phase‐transfer catalyst by simple extraction with fluorous solvents.     

Alkane Oxidation by an Immobilized Nickel Complex Catalyst: Structural and Reactivity Differences Induced by Surface‐Ligand Density on Mesoporous Silica

Immobilized nickel catalysts SBA*‐ L ‐x/Ni ( L =bis(2‐pyridylmethyl)(1H‐1,2,3‐triazol‐4‐ylmethyl)amine) with various ligand densities ( L content (x)=0.5, 1, 2, 4 mol % Si) have been prepared from azidopropyl‐functionalized mesoporous silicas SBA‐N₃‐x. Related homogeneous ligand LtBu and its Ni^II complexes, [Ni( LtBu )(OAc)₂(H₂O)] ( LtBu /Ni) and [Ni( LtBu )₂]BF₄ (2 LtBu /Ni), have been synthesized. The L /Ni ratio (0.9–1.7:1) in SBA*‐ L ‐x/Ni suggests the formation of an inert [Ni L ₂] site on the surface at higher ligand loadings. SBA*‐ L ‐x/Ni has been applied to the catalytic oxidation of cyclohexane with m‐chloroperbenzoic acid (mCPBA). The catalyst with the lowest loading shows high activity in its initial use as the homogeneous LtBu /Ni catalyst, with some metal leaching. As the ligand loading increases, the activity and Ni leaching are suppressed. The importance of site‐density control for the development of immobilized catalysts has been demonstrated.     

Modulation of Multifunctional N,O,P Ligands for Enantioselective Copper‐Catalyzed Conjugate Addition of Diethylzinc and Trapping of the Zinc Enolate

In this work, we have successfully synthesized a new family of chiral Schiff base–phosphine ligands derived from chiral binaphthol (BINOL) and chiral primary amine. The controllable synthesis of a novel hexadentate and tetradentate N,O,P ligand that contains both axial and sp³‐central chirality from axial BINOL and sp³‐central primary amine led to the establishment of an efficient multifunctional N,O,P ligand for copper‐catalyzed conjugate addition of an organozinc reagent. In the asymmetric conjugate reaction of organozinc reagents to enones, the polymer‐like bimetallic multinuclear Cu? Zn complex constructed in situ was found to be substrate‐selective and a highly excellent catalyst for diethylzinc reagents in terms of enantioselectivity (up to >99 % ee). More importantly, the chirality matching between different chiral sources, C₂‐axial binaphthol and sp³‐central chiral phosphine, was crucial to the enantioselective induction in this reaction. The experimental results indicated that our chiral ligand (R,S,S)‐ L1 ‐ and (R,S)‐ L4 ‐based bimetallic complex catalyst system exhibited the highest catalytic performance to date in terms of enantioselectivity and conversion even in the presence of 0.005 mol % of catalyst (S/C=20 000, turnover number (TON)=17 600). We also studied the tandem silylation or acylation of enantiomerically enriched zinc enolates that formed in situ from copper‐ L4 ‐complex‐catalyzed conjugate addition, which resulted in the high‐yield synthesis of chiral silyl enol ethers and enoacetates, respectively. Furthermore, the specialized structure of the present multifunctional N,O,P ligand L1 or L4 , and the corresponding mechanistic study of the copper catalyst system were investigated by ³¹P NMR spectroscopy, circular dichroism (CD), and UV/Vis absorption.     

Three‐Component Asymmetric Catalytic Ugi Reaction—Concinnity from Diversity by Substrate‐Mediated Catalyst Assembly

The first chiral catalyst for the three‐component Ugi reaction was identified as a result of a screen of a large set of different BOROX catalysts. The BOROX catalysts were assembled in situ from a chiral biaryl ligand, an amine, water, BH₃?SMe₂ , and an alcohol or phenol. The catalyst screen included 13 different ligands, 12 amines, and 47 alcohols or phenols. The optimal catalyst system (LAP 8‐5‐47) provided α‐amino amides from an aldehyde, a secondary amine, and an isonitrile with excellent asymmetric induction. The catalytically active species is proposed to be an ion pair that consists of the chiral boroxinate anion and an iminium cation.     

Synthesis of Novel Monodentate Phosphoramidites and Their Application in Iridium‐Catalyzed Asymmetric Hydrogenations

New monodentate H₈‐binaphthol based phosphoramidites 6 b–i have been prepared. Starting from (S)‐3,3′‐dibromo‐5,5′,6,6′,7,7′,8,8′‐octahydro‐1,1′‐binaphthyl‐2,2′‐diol 3 , a general protocol for the synthesis of ligands 6 is presented. A small ligand library bearing aryl substituents in the 3,3′‐position of the binaphthol core was synthesized and successfully tested in the iridium‐catalyzed asymmetric hydrogenation of 2‐amidocinnamates to obtain different α‐amino acid derivatives in up to 99 % ee.     

Pincer and diamine Ru and Os diphosphane complexes as efficient catalysts for the dehydrogenation of alcohols to ketones

The ruthenium and osmium complexes [MCl₂(diphosphane)(L)] (M=Ru, Os; L=bidentate amino ligand) and [MCl(CNN)(dppb)] (CNN=pincer ligand; dppb=1,4‐bis‐ (diphenylphosphino)butane), containing the N–H moiety, have been found to catalyze the acceptorless dehydrogenation of alcohols in tBuOH and in the presence of KOtBu. The compounds trans‐[MCl₂(dppf)(en)] (M=Ru 7 , Os 13 ; dppf=1,1′‐bis(diphenylphosphino)ferrocene; en=ethylenediamine) display very high activity and different substrates, including cyclic and linear alcohols, are efficiently oxidized to ketones by using 0.8–0.04 mol % of catalyst. The effect of the base and the comparison of the catalytic activity of the Ru versus Os complexes are reported. The ruthenium complex 7 generally leads to a faster conversion into ketones with respect to the osmium complex 13 , which displays better activity in the dehydrogenation of 5‐en‐3β‐hydroxy steroids. The synthesis of new Ru and Os complexes [MCl₂(PP)(L)] (PP=dppb, dppf; L=(±)‐trans‐1,2‐diaminocyclohexane, 2‐(aminomethyl)pyridine, and 2‐aminoethanol) of trans and cis configuration is also reported.     

Chirality‐ and pH‐Controlled Supramolecular Isomerism in Cobalt Phosphonates and Its Impact on the Magnetic Behavior

Two pairs of enantiomeric compounds with formulas (S)‐ or (R)‐Co₃(ppap)₂(4,4′‐bpy)₂(H₂O)₂ ? 4 H₂O [(S)‐ 1 or (R)‐ 1 ], (S)‐ or (R)‐Co₃(ppap)₂(4,4′‐bpy)₂(H₂O)₂ ? 3 H₂O [(S)‐ or (R)‐ 2 ), and related racemic compound Co₃(ppap)₂(4,4′‐bpy)₂(H₂O)₂ ? 4 H₂O (rac‐ 3 ; 4,4′‐bpy=4,4′‐bipyridine, H₃ppap=3‐phenyl‐2‐[(phosphonomethyl)amino]propanoic acid) are reported. Compounds 1 and rac‐ 3 show identical three‐dimensional framework structures, whereas compounds 2 have two‐dimensional layer structures. Compounds 1 and 2 are catenation isomers, formation of which is controlled solely by the pH of the reaction mixtures, whereas the formation of isomeric compounds 1 and rac‐ 3 is controlled purely by the chirality of the phosphonate ligand. The magnetic properties of fully dehydrated (S)‐ 1 , (S)‐ 2 , and rac‐ 3 are highly dependent on both structure and chirality.     

A Highly Efficient and Broadly Applicable Cationic Gold Catalyst

Gold catalysts capable of promoting reactions at low‐level loadings under mild conditions are the exception rather than the norm. We examined reactions where the regeneration of cationic gold catalyst (e.g., protodeauration) was the turnover limiting stage. By manipulating electron density on the substituents around phosphorus and introducing steric handles we designed a phosphine ligand that contains two electron‐rich ortho‐biphenyl groups and a cyclohexyl substituent. This ligand formed a gold complex that catalyzed common types of gold‐catalyzed reactions including intra‐ and intermolecular X? H (X=C, N, O) additions to alkynes and cycloisomerizations, with high turnover numbers at room temperature or slightly elevated temperatures (≤50 °C). Our new ligand can be prepared in one step from commercially available starting materials.     

Catalytic asymmetric aziridination with borate catalysts derived from VANOL and VAPOL ligands: scope and mechanistic studies

An extended study of the scope and mechanism of the catalytic asymmetric aziridination of imines with ethyl diazoacetate mediated by catalysts prepared from the VANOL and VAPOL ligands and triphenylborate is described. Nonlinear studies with scalemic VANOL and VAPOL reveal an essentially linear relationship between the optical purity of the ligand and the product suggesting that the catalyst incorporates a single molecule of the ligand. Two species are present in the catalyst prepared from B(OPh)(3) and either VANOL or VAPOL as revealed by (1)H NMR studies. Mass spectral analysis of the catalyst mixture suggests that one of the species involves one ligand molecule and one boron atom (B1) and the other involves one ligand and two boron atoms (B2). The latter can be formulated as either a linear or cyclic pyroborate and the (11)B NMR spectrum is most consistent with the linear pyroborate structure. Several new protocols for catalyst preparation are developed which allow for the generation of mixtures of the B1 and B2 catalysts in ratios that range from 10:1 to 1:20. Studies with catalysts enriched in the B1 and B2 species reveal that the B2 catalyst is the active catalyst in the VAPOL catalyzed asymmetric aziridination reaction giving significantly higher asymmetric inductions and rates than the B1 catalyst. The difference is not as pronounced in the VANOL series. A series of 12 different imines were surveyed with the optimal catalyst preparation procedure with the finding that the asymmetric inductions are in the low to mid 90s for aromatic imines and in the mid 80s to low 90s for aliphatic imines for both VANOL and VAPOL catalysts. Nonetheless, the crystallinity of the N-benzhydryl aziridines is such that nearly all of the 12 aziridine products screened can be brought to >99 % ee with a single recrystallization.     

The Control of the Stereochemistry in the Palladium‐Catalyzed Alternating Styrene/Carbon Monoxide Copolymerization: Effect of the Chirality of the Ligand and of the Ligand‐to‐Palladium Ratio,Preliminary Communication

Diaquapalladium(2+) trifluoromethanesulfonates modified with (4R,4′S)‐ or (4S,4′S)‐2,2′‐bis(4‐benzyl‐4,5‐dihydrooxazole) (C_s‐ and C₂‐ligands) produce isotactic poly(1‐oxo‐2‐phenylpropane‐1,3‐diyl) through copolymerization of styrene with carbon monoxide. However, the same meso‐catalyst in the presence of the free ligand leads to prevailingly syndiotactic growth of the copolymer, whereas the optically active catalyst, when used in the presence of the free enantiomeric ligand, gives an atactic copolymer.     

Acid‐, Water‐ and High‐Temperature‐Stable Ruthenium Complexes for the Total Catalytic Deoxygenation of Glycerol to Propane

The ruthenium aqua complexes [Ru(H₂O)₂(bipy)₂](OTf)₂, [cis‐Ru(6,6′‐Cl₂‐bipy)₂(OH₂)₂](OTf)₂, [Ru(H₂O)₂(phen)₂](OTf)₂, [Ru(H₂O)₃(2,2′:6′,2′′‐terpy)](OTf)₂ and [Ru(H₂O)₃(Phterpy)](OTf)₂ (bipy=2,2′‐bipyridine; OTf^?=triflate; phen=phenanthroline; terpy= terpyridine; Phterpy=4′‐phenyl‐2,2′:6′,2′′‐terpyridine) are water‐ and acid‐stable catalysts for the hydrogenation of aldehydes and ketones in sulfolane solution. In the presence of HOS(O)₂CF₃ (triflic acid) as a dehydration co‐catalyst they directly convert 1,2‐hexanediol to n‐hexanol and hexane. The terpyridine complexes are stable and active as catalysts at temperatures ≥250 °C and in either aqueous sulfolane solution or pure water convert glycerol into n‐propanol and ultimately propane as the final reaction product in up to quantitative yield. For the terpy complexes the active catalyst is postulated to be a carbonyl species [(4′‐R‐2,2′:6′,2′′‐terpy)Ru(CO)(H₂O)₂](OTf)₂ (R=H, Ph) formed by the decarbonylation of aldehydes (hexanal for 1,2‐hexanediol and 3‐hydroxypropanal for glycerol) generated in the reaction mixture through acid‐catalyzed dehydration. The structure of the dimeric complex [{(4′‐phenyl‐2,2′:6′,2′′‐terpy)Ru(CO)}₂(μ‐OCH₃)₂](OTf)₂ has been determined by single crystal X‐ray crystallography (Space group P (a=8.2532(17); b=12.858(3); c=14.363(3) Å; α=64.38(3); β=77.26(3); γ = 87.12(3)°, R=4.36 %).     

BINAP versus BINAP(O) in asymmetric intermolecular Mizoroki-Heck reactions: substantial effects on selectivities

2,2′‐Bis(diphenylphosphino)‐1,1′‐binaphthyl (BINAP) was employed as chiral ligand in the enantioselective intermolecular Mizoroki–Heck reaction, whereas the use of cognate BINAP(O) (monooxidized BINAP) is unprecedented. The regio‐ and enantioselectivity of the arylation of representative cyclic alkenes changes dramatically in the presence of hemilabile BINAP(O) instead of BINAP. The arylation of 2,3‐dihydrofuran is perfectly regiodivergent (98:2 versus 0:100) and the arylation of cyclopentene is only enantioselective with BINAP(O) [60 versus 10 % enantiomeric excess (ee)]. Use of [Pd₂(dba)₃] ? dba (dba=dibenzylideneacetone) instead of Pd(OAc)₂ produces as high as 86 % ee in the arylation of cyclopentene.     

Enantioselective Double Manipulation of Tetrahydroisoquinolines with Terminal Alkynes and Aldehydes under Copper(I) Catalysis

Tetrahydroisoquinoline alkaloids with a C1 stereogenic center are a common unit in many natural and non‐natural compounds of biological importance. Herein we describe a novel Cu^I‐catalyzed highly chemo‐ and enantioselective synthesis of chiral tetrahydroisoquinoline‐alkaloid derivatives from readily available unsubstituted tetrahydroisoquinolines, aldehydes, and terminal alkynes in the presence of the ligand (R,R)‐N‐pinap. This synthetic operation installs two substituents in the 1‐ and 2‐positions.     

A New Modular Phosphite‐Pyridine Ligand Library for Asymmetric Pd‐Catalyzed Allylic Substitution Reactions: A Study of the Key Pd‐π‐Allyl Intermediates

A library of phosphite‐pyridine ligands L1 – L12 a – g has been successfully applied for the first time in the Pd‐catalyzed allylic substitution reactions of several di‐ and trisubstituted substrates by using a wide range of C, N and O nucleophiles, among which are the little studied α‐substituted malonates, β‐diketones, and alkyl alcohols. The highly modular nature of this ligand library enables the substituents/configuration at the ligand backbone, and the substituents/configurations at the biaryl phosphite moiety to be easily and systematically varied. We found that the introduction of an enantiopure biaryl phosphite moiety played an essential role in increasing the versatility of the Pd‐catalytic systems. Enantioselectivities were therefore high for several hindered and unhindered di‐ and trisubstituted substrates by using a wide range of C, N and O nucleophiles. Of particular note were the high enantioselectivities (up to>99 % ee) and high activities obtained for the trisubstituted substrates S6 and S7 , which compare favorably with the best that have been reported in the literature. We have also extended the use of these new catalytic systems in alternative environmentally friendly solvents such as propylene carbonate and ionic liquids. Studies on the Pd‐π‐allyl intermediates provide a deeper understanding of the effect of ligand parameters on the origin of enantioselectivity.     

Total Syntheses and Biological Evaluation of Both Enantiomers of Several Hydroxylated Dimeric Nuphar Alkaloids

Herein, we describe the first total syntheses of five members of the dimeric nuphar alkaloids: (+)‐6,6′‐dihydroxythiobinupharidine (+)‐ 1 a , (+)‐6‐hydroxythiobinupharidine (+)‐ 1 b , (?)‐6,6′‐dihydroxythionuphlutine (?)‐ 2 a , (?)‐6,6′‐dihydroxyneothiobinupharidine (?)‐ 3 a , and (+)‐6,6′‐dihydroxyneothionuphlutine (+)‐ 4 a . The latter two have not been found in nature. We have also made each of their enantiomers (?)‐ 1 a – b , (+)‐ 2 a , (+)‐ 3 a , and (?)‐ 4 a . The key step in these syntheses was the dimerization of an α‐aminonitrile (a hydrolytically stable surrogate for its corresponding hemiaminal) with chiral Lewis acid complexes. We have also reassigned the literature structures of (+)‐ 1 a – 1 b —for those instances in which the NMR spectra were obtained in CD₃OD—to their corresponding CD₃O‐adducts. Our efforts provide for the first time apoptosis data for (?)‐ 3 a , (+)‐ 4 a , and all five non‐natural enantiomers prepared. The data indicate high apoptotic activity regardless of the enantiomer or relative stereochemical configuration at C7 and C7′.     

Copper‐Complex‐Catalyzed Asymmetric Aerobic Oxidative Cross‐Coupling of 2‐Naphthols: Enantioselective Synthesis of 3,3′‐Substituted C1‐Symmetric BINOLs

A novel chiral 1,5‐N,N‐bidentate ligand based on a spirocyclic pyrrolidine oxazoline backbone was designed and prepared, and it coordinates CuBr in situ to form an unprecedented catalyst that enables efficient oxidative cross‐coupling of 2‐naphthols. Air serves as an external oxidant and generates a series of C₁‐symmetric chiral BINOL derivatives with high enantioselectivity (up to 99 % ee) and good yield (up to 87 %). This approach is tolerant of a broader substrates scope, particularly substrates bearing various 3‐ and 3′‐substituents. A preliminary investigation using one of the obtained C₁‐symmetric BINOL products was used as an organocatalyst, exhibiting better enantioselectivity than the previously reported organocatalyst, for the asymmetric α‐alkylation of amino esters.