Stereo- and regioselectivity of the hetero-Diels–Alder reaction of nitroso derivatives with conjugated dienes

• Lucie Brulíková,
• Aidan Harrison,
• Marvin J. Miller and
• Jan Hlaváč

Beilstein J. Org. Chem. 2016, 12, 1949–1980, doi:10.3762/bjoc.12.184

• substrates: a) reaction with chiral nitroso dienophiles; b) reaction with a chiral diene; and c) reaction via double asymmetric induction, with both the diene and nitroso dienophile being chiral entities. Chiral dienophiles: The use of acylnitroso dienophiles with chiral auxiliaries has ample precedent in

• used by Orena in reactions with cyclopentadiene and cyclohexadiene, giving the products with de values of 74 and 86%, respectively [118]. A series of chiral auxiliaries based on mandelic acid showed similar stereoselectivity benefits and have been proposed by Procter for stereoselective synthesis [109

Experimental and theoretical insights in the alkene–arene intramolecular π-stacking interaction

• Valeria Corne,
• Ariel M. Sarotti,
• Carmen Ramirez de Arellano,
• Rolando A. Spanevello and
• Alejandra G. Suárez

Beilstein J. Org. Chem. 2016, 12, 1616–1623, doi:10.3762/bjoc.12.158

•  1). Saponification of adducts 11 and 12 provided the free 5-norbornenecarboxylic acid and the chiral auxiliaries 5a and 5b in excellent yields, which can be reused. Conclusion We have reported the synthesis of chiral acrylates derived from renewable feedstock as models to study arene–alkene π

Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction

• Samantha Caputo,
• Andrea Basso,
• Lisa Moni,
• Renata Riva,
• Valeria Rocca and
• Luca Banfi

Beilstein J. Org. Chem. 2016, 12, 139–143, doi:10.3762/bjoc.12.15

• /epimerization can again be an issue in special cases [24]. However, the use of amines as chiral auxiliaries has been seldom exploited in peptidomimetic synthesis [16][25][26] because the need to remove the auxiliary reduces the number of diversity inputs and increases the number of synthetic steps. From the

• point of view of atom- and step-economy, the use of chiral amines that are retained in the final products will be more valuable [27]. In this case they are not "chiral auxiliaries" and are not removed after the multicomponent reaction, and they contribute to the diversity of the final products. However

Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams

• Katherine M. Byrd

Beilstein J. Org. Chem. 2015, 11, 530–562, doi:10.3762/bjoc.11.60

• development of asymmetric variants of the Michael reaction. In early studies, chemists relied on chiral auxiliaries [5], heterocuprates [15][16], or natural product-based [17] ligands to induce high to modest stereoselectivity. In 1991, Alexandre Alexakis and co-workers reported the first asymmetric conjugate

• lactams. 1.1 DCA using chiral auxiliaries Chiral auxiliaries have been useful tools to induce stereoselectivity in C–C bond forming reactions [5][32][33][34]. Ideally, these compounds are stable, easily attached, removed and recoverable. One of the first examples of a DCA reaction using a chiral auxiliary

• the oxygen of the resulting enolate of the CA reaction. This chelation to the magnesium would retard the 1,2-addition reaction from occurring. Since the Mukaiyama publication, there have been many chiral auxiliaries studied in DCA reactions of α,β-unsaturated amides [35]. Figure 2 highlights a few of

Metal-free one-pot synthesis of 2-substituted and 2,3-disubstituted morpholines from aziridines

• Hongnan Sun,
• Binbin Huang,
• Run Lin,
• Chao Yang and
• Wujiong Xia

Beilstein J. Org. Chem. 2015, 11, 524–529, doi:10.3762/bjoc.11.59

• cis-2,3-disubstituted morpholine, aprepitant, is approved for the use in the prevention of chemotherapy-induced nausea and vomiting [6]. In addition to pharmacological properties, morpholines are also used in organic synthesis as bases, catalysts, and chiral auxiliaries [7][8][9][10][11][12][13]. Thus

(2R,1'S,2'R)- and (2S,1'S,2'R)-3-[2-Mono(di,tri)fluoromethylcyclopropyl]alanines and their incorporation into hormaomycin analogues

• Armin de Meijere,
• Sergei I. Kozhushkov,
• Dmitrii S. Yufit,
• Christian Grosse,
• Marcel Kaiser and
• Vitaly A. Raev

Beilstein J. Org. Chem. 2014, 10, 2844–2857, doi:10.3762/bjoc.10.302

• -threonine (4) and (2S,3R)-β-methylphenylalanine (3), using the Belokon' approach with (S)- and (R)-2-[(N-benzylprolyl)amino]benzophenone [(S)- and (R)-10] as reusable chiral auxiliaries have been developed. Three new fluoromethyl analogues of the naturally occurring octadepsipeptide hormaomycin (1) with

• from (S)- and (R)-2-[(N-benzylprolyl)amino]benzophenone [(S)- and (R)-10] as reusable chiral auxiliaries with the racemic iodides 11a–c, employing the protocol of Larionov and de Meijere [7], in each case led to a mixture of diastereomeric products, which were separated by column chromatography

One-pot stereoselective synthesis of α,β-differentiated diamino esters via the sequence of aminochlorination, aziridination and intermolecular S_N2 reaction

• Yiwen Xiong,
• Ping Qian,
• Chenhui Cao,
• Haibo Mei,
• Jianlin Han,
• Guigen Li and
• Yi Pan

Beilstein J. Org. Chem. 2014, 10, 1802–1807, doi:10.3762/bjoc.10.189

• corresponding β,γ-amino alcohols and vicinal diamines. α,β-Diamino acid derivatives have been served as organocatalysts, chiral ligands, chiral auxiliaries for asymmertric synthesis [10][11][12], as well as synthetic fragments for peptides and natural products [13]. Mannich-type addition reactions of α-amino

Asymmetric Ugi 3CR on isatin-derived ketimine: synthesis of chiral 3,3-disubstituted 3-aminooxindole derivatives

• Giordano Lesma,
• Fiorella Meneghetti,
• Alessandro Sacchetti,
• Mattia Stucchi and
• Alessandra Silvani

Beilstein J. Org. Chem. 2014, 10, 1383–1389, doi:10.3762/bjoc.10.141

• created, the stereoselectivity remains a difficult task. Waiting for enantioselective versions of the Ugi reaction [29][30][31], the diastereoselective approach by using chiral material is a possible solution. In particular, amines have shown to be promising as chiral auxiliaries, even though only a few

Preparation of phosphines through C–P bond formation

• Iris Wauters,
• Wouter Debrouwer and
• Christian V. Stevens

Beilstein J. Org. Chem. 2014, 10, 1064–1096, doi:10.3762/bjoc.10.106

• halophosphines and their weak configurational stability. P-stereogenic chlorophosphines racemize easily even at room temperature [30]. Enantiopure P-stereogenic compounds can be synthesized via a diastereoselective nucleophilic substitution at phosphorus utilizing chiral auxiliaries. Diastereomeric intermediates

• are formed that are separable by chromatography or recrystallization. The protocol has proven to be effective and has become the preferred approach for the synthesis of chiral phosphines. Commonly used chiral auxiliaries are chiral secondary alcohols (for example (−)-menthol (3), endo-borneol, etc

Group-assisted purification (GAP) chemistry for the synthesis of Velcade via asymmetric borylation of N-phosphinylimines

• Jian-bo Xie,
• Jian Luo,
• Timothy R. Winn,
• David B. Cordes and
• Guigen Li

Beilstein J. Org. Chem. 2014, 10, 746–751, doi:10.3762/bjoc.10.69

• -catalyzed borylation of the imine anchored with chiral auxiliaries [16][17]; (3) to conduct asymmetric catalytic hydrogenation as the key step to control the chiral center of boronic aicd [18]. As anticipated, the above known syntheses required traditional purification methods using column chromatography or

Synthesis of complex intermediates for the study of a dehydratase from borrelidin biosynthesis

• Frank Hahn,
• Nadine Kandziora,
• Steffen Friedrich and
• Peter F. Leadlay

Beilstein J. Org. Chem. 2014, 10, 634–640, doi:10.3762/bjoc.10.55

• as on aldehyde 11 [18][19][20][21]. However, in all these cases either the aldol reaction itself proved to be low yielding (<20%) or removal conditions of chiral auxiliaries were destructive to the molecule. The best results were obtained for an anti-selective variant, in which aldehyde 11 was

Concise, stereodivergent and highly stereoselective synthesis of cis- and trans-2-substituted 3-hydroxypiperidines – development of a phosphite-driven cyclodehydration

• Peter H. Huy,
• Julia C. Westphal and
• Ari M. P. Koskinen

Beilstein J. Org. Chem. 2014, 10, 369–383, doi:10.3762/bjoc.10.35

• active natural products [1][2][3][4][5][6][7][8][9], chiral auxiliaries [10][11] and catalysts for asymmetric synthesis [12][13][14]. Especially the 2-substituted 3-hydroxypiperidine scaffold of the general structure B (as one type of an 1,2-amino alcohol) can be found in numerous natural products and

Stereodivergent synthesis of jaspine B and its isomers using a carbohydrate-derived alkoxyallene as C₃-building block

• Volker M. Schmiedel,
• Stefano Stefani and
• Hans-Ulrich Reissig

Beilstein J. Org. Chem. 2013, 9, 2564–2569, doi:10.3762/bjoc.9.291

• . Keywords: chiral auxiliaries; gold catalysis; jaspine B; lithiated alkoxyallenes; natural product synthesis; pachastrissamine; tetrahydrofurans; Introduction Jaspine B, also known as pachastrissamine (1, Scheme 1), is an anhydrophytosphingosine derivative, isolated 2002 from the marine sponge Pachastrissa

• Having established suitable conditions for the construction of the functionalized tetrahydrofuran core we focused our attention on the synthesis of enantiopure jaspine B (1). Earlier investigations by Goré [38] and our group already showed the feasibility of alkoxyallenes with carbohydrate-derived chiral

• auxiliaries for the synthesis of enantiopure natural products such as preussin [39] and anisomycin [40] or in hetero Diels–Alder reactions [41][42]. For the stereodivergent synthesis of both enantiomers of jaspine B (1), we chose diacetoneglucose-derived alkoxyallene 11, which is easily accessible on gram

Non-cross-linked polystyrene-supported 2-imidazolidinone chiral auxiliary: synthesis and application in asymmetric alkylation reactions

• Quynh Pham Bao Nguyen and
• Taek Hyeon Kim

Beilstein J. Org. Chem. 2013, 9, 2113–2119, doi:10.3762/bjoc.9.248

• -imidazolidinone chiral auxiliaries were successfully investigated with excellent diastereocontrol (>99% de). The recovery and the recycling of this soluble polymer-supported chiral auxiliary were achieved in order to produce highly optical pure carboxylic acids. Keywords: asymmetric alkylation; chiral

• auxiliaries; chiral carboxylic acids; 2-imidazolidinone; non-cross-linked polystyrene; Introduction Chiral auxiliaries have been proven as a powerful tool for the asymmetric synthesis of highly optical pure compounds used in pharmaceuticals or agrochemicals [1][2]. The recycling and reuse of expensive chiral

• auxiliaries is a challenge in organic synthesis and remains under-developed [3]. In this field, polymer-supported synthesis has emerged as a versatile technique, which involves the attachment of chiral auxiliaries to the polymer carriers for convenient purification, recovery and reuse. Most recently, cross

Enantioselective synthesis of planar chiral ferrocenes via palladium-catalyzed annulation with diarylethynes

• Yan-Chao Shi,
• Rong-Fei Yang,
• De-Wei Gao and
• Shu-Li You

Beilstein J. Org. Chem. 2013, 9, 1891–1896, doi:10.3762/bjoc.9.222

• planar chirality are applied as efficient ligands or catalysts in asymmetric catalysis [5][6][7][8][9][10][11][12][13][14][15]. However, the typical method for introduction of planar chirality in the ferrrocene backbone is still utilizing the chiral auxiliaries strategy [16][17][18][19][20][21]. Snieckus

A versatile and efficient approach for the synthesis of chiral 1,3-nitroamines and 1,3-diamines via conjugate addition to new (S,E)-γ-aminated nitroalkenes derived from L-α-amino acids

• Vera Lúcia Patrocinio Pereira,
• André Luiz da Silva Moura,
• Daniel Pais Pires Vieira,
• Leandro Lara de Carvalho,
• Eliz Regina Bueno Torres and
• Jeronimo da Silva Costa

Beilstein J. Org. Chem. 2013, 9, 832–837, doi:10.3762/bjoc.9.95

• enantioselective synthesis as chiral auxiliaries, chiral catalysts, chiral reagents and chiral ligands [59][60]. In our continuing interest in synthesizing new chiral nonracemic nitro compounds [61][62][63][64][65][66][67][68] by a "chiron" approach [45], we intended to develop a route for obtaining γ-nitrogenated

Chemoenzymatic synthesis and biological evaluation of enantiomerically enriched 1-(β-hydroxypropyl)imidazolium- and triazolium-based ionic liquids

• Paweł Borowiecki,
• Małgorzata Milner-Krawczyk and
• Jan Plenkiewicz

Beilstein J. Org. Chem. 2013, 9, 516–525, doi:10.3762/bjoc.9.56

• to the stereogenic center of the alcohol in the same plane. The differences in the chemical shifts (ΔδRS) observed in the spectra of the esters prepared from the chiral auxiliaries [(R)- and (S)-MPA acids, respectively], were calculated separately for the protons attached to the carbon atoms situated

Asymmetric Diels–Alder reaction with >C=P– functionality of the 2-phosphaindolizine-η¹-P-aluminium(O-menthoxy) dichloride complex: experimental and theoretical results

• Rajendra K. Jangid,
• Nidhi Sogani,
• Neelima Gupta,
• Raj K. Bansal,
• Moritz von Hopffgarten and
• Gernot Frenking

Beilstein J. Org. Chem. 2013, 9, 392–400, doi:10.3762/bjoc.9.40

• ; DFT calculations Diels–Alder reaction; Introduction There is an increasing emphasis on the synthesis of optically pure compounds, as far as possible, for environmental, economic and social reasons. Using chiral auxiliaries for changing enantiotopic faces into diastereotopic faces is a common approach

• developed [2]. The chiral pool continues to be an attractive and economic source of enantiomerically pure chiral auxiliaries (ligands or modifiers) for enantioselective synthesis [3]. Two naturally occurring enantiomers of menthol and synthetically prepared (1R)-(+)-8-phenylmenthol have often been used as

• chiral auxiliaries [3][4]. Chiral phosphines constitute a very important group of ligands as their coordination compounds with transition metals have been extensively employed in asymmetric catalysis to convert achiral compounds into enantio-enriched products with high efficiency and enantioselectivity

trans-2-(2,5-Dimethoxy-4-iodophenyl)cyclopropylamine and trans-2-(2,5-dimethoxy-4-bromophenyl)cyclopropylamine as potent agonists for the 5-HT₂ receptor family

• Adam Pigott,
• Stewart Frescas,
• John D. McCorvy,
• Xi-Ping Huang,
• Bryan L. Roth and
• David E. Nichols

Beilstein J. Org. Chem. 2012, 8, 1705–1709, doi:10.3762/bjoc.8.194

• chiral auxiliaries in the cyclopropanation step could directly afford the chiral cyclopropane acids [8], but time and resources did not allow us to pursue that approach. Conclusion In conclusion, our strategy to replace the ethylamine side chain of 1a (or 1b) with a cyclopropylamine moiety was successful

Carbohydrate-auxiliary assisted preparation of enantiopure 1,2-oxazine derivatives and aminopolyols

• Marcin Jasiński,
• Dieter Lentz and
• Hans-Ulrich Reissig

Beilstein J. Org. Chem. 2012, 8, 662–674, doi:10.3762/bjoc.8.74

• samarium diiodide leading to enantiopure acyclic aminopolyols. We also report on our attempts to convert these compounds into enantiopure hydroxylated pyrrolidine derivatives. Keywords: aminopolyols; carbohydrates; chiral auxiliaries; lithiated alkoxyallenes; 1,2-oxazines; pyrroles; pyrrolidines; samarium

Continuous-flow enantioselective α-aminoxylation of aldehydes catalyzed by a polystyrene-immobilized hydroxyproline

• Xacobe C. Cambeiro,
• Rafael Martín-Rapún,
• Pedro O. Miranda,
• Sonia Sayalero,
• Esther Alza,
• Patricia Llanes and
• Miquel A. Pericàs

Beilstein J. Org. Chem. 2011, 7, 1486–1493, doi:10.3762/bjoc.7.172

• preformed enolates, both with the use of chiral auxiliaries (chiral, enantiopure enolates and achiral oxidizing agents, or achiral enolates and chiral, enantiopure oxidizing agents) [3][4][5] and by Mukaiyama-type catalytic processes involving preformed achiral enolate equivalents and achiral oxidants, with

Alkene selenenylation: A comprehensive analysis of relative reactivities, stereochemistry and asymmetric induction, and their comparisons with sulfenylation

• Vadim A. Soloshonok and
• Donna J. Nelson

Beilstein J. Org. Chem. 2011, 7, 744–758, doi:10.3762/bjoc.7.85

• reactivity of organoselenium compounds, it is expected that chiral selenium containing derivatives could be synthetically useful as chiral auxiliaries or intermediates for the development of a novel asymmetric methodology platform [15][16][17][18]. Furthermore, compared with sulfur analogs [44], chiral

• considered generally more efficient chiral auxiliaries compared with compound 1 [27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43]. Reactions of benzeneselenenyl halides, including chiral compounds 1–3, with alkenes generally [55][56] exhibit high Markovnikov regioselectivity [57], with

Effects of anion complexation on the photoreactivity of bisureido- and bisthioureido-substituted dibenzobarrelene derivatives

• Heiko Ihmels and
• Jia Luo

Beilstein J. Org. Chem. 2011, 7, 278–289, doi:10.3762/bjoc.7.37

• asymmetric photoreactions have been conducted with remarkable enantioselectivity in homogeneous solution, whereas reports of asymmetric di-π-methane rearrangements in solutions are relatively rare. Chiral auxiliaries attached as ester or amide functionalities at the vinylic positions of dibenzobarrelene

Enantioselective synthesis of tricyclic amino acid derivatives based on a rigid 4-azatricyclo[5.2.1.0^2,6]decane skeleton

• Matthias Breuning,
• Tobias Häuser,
• Christian Mehler,
• Christian Däschlein,
• Carsten Strohmann,
• Andreas Oechsner and
• Holger Braunschweig

Beilstein J. Org. Chem. 2009, 5, No. 81, doi:10.3762/bjoc.5.81

• β-turn-inducing building blocks in peptidomimetics and for chiral auxiliaries in asymmetric organocatalysis. Keywords: amino acid; enantioselective synthesis; norbornane; polycyclic compounds; pyrrolidine; Introduction Unnatural amino acids with a rigid bowl-shaped backbone have received

• are promising candidates as ß-turn-inducing building blocks in peptidomimetics and as chiral auxiliaries in organocatalysis. The conformationally rigid amino acid derivatives 1–3 (β-turn-inducing building blocks) and 4–6 (successful organocatalysts). The targeted tricyclic amino acid derivatives 7 and

Conformational rigidity of silicon- stereogenic silanes in asymmetric catalysis: A comparative study

• Sebastian Rendler and
• Martin Oestreich

Beilstein J. Org. Chem. 2007, 3, No. 9, doi:10.1186/1860-5397-3-9

• based on silicon-stereogenic reagents or substrates were revisited or invented. [1][2][3][4] Aside from the use of silicon-stereogenic chiral auxiliaries in substrate-controlled reactions, [5] a still limited number of remarkable stereoselective processes with a stereogenic silicon as the reactive site