Advancements in hydrochlorination of alkenes

• Daniel S. Müller

Beilstein J. Org. Chem. 2024, 20, 787–814, doi:10.3762/bjoc.20.72

• ]. It is important to note that we are not aware of any catalytic enantioselective hydrochlorination reactions of alkenes. Conjugate additions of HCl to a complex of α,β-unsaturated acids, incorporated in an α-cyclodextrin, which corresponds to a formal hydrochlorination was reported by Tanaka and co

Catalytic multi-step domino and one-pot reactions

• Svetlana B. Tsogoeva

Beilstein J. Org. Chem. 2024, 20, 254–256, doi:10.3762/bjoc.20.25

• stereocenters [7]. In the Review paper by Kisszékelyi and Šebesta, the diverse variety of chiral metal enolates obtained by asymmetric conjugate additions of organometallic reagents and the possibilities to engage metal enolates in tandem reactions with new electrophiles are presented [8]. A Perspective from X

Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review

• Nosheen Beig,
• Varsha Goyal and
• Raj K. Bansal

Beilstein J. Org. Chem. 2023, 19, 1408–1442, doi:10.3762/bjoc.19.102

• , Me, C≡C-n-hep, Ph, CO2Me) and trialkylaluminum (alkyl = Me, Et, iBu) were used for the reactions. This approach is particularly attractive for asymmetric conjugate additions to pentenones, which are otherwise difficult to accomplish. 2.2.3 Reaction with organoboron reagents: In 2010, Hoveyda and co

Asymmetric tandem conjugate addition and reaction with carbocations on acylimidazole Michael acceptors

• Brigita Mudráková,
• Renata Marcia de Figueiredo,
• Jean-Marc Campagne and
• Radovan Šebesta

Beilstein J. Org. Chem. 2023, 19, 881–888, doi:10.3762/bjoc.19.65

• obtained by other conjugate addition reactions. Keywords: acylimidazole; asymmetric catalysis; carbocation; conjugate addition; enolate; Introduction Asymmetric metal-catalyzed conjugate additions provide access to numerous chiral scaffolds. This type of C–C bond formation efficiently enables the

• construction of stereogenic centers using polar organometallics [1]. In this way, 1,4-additions of typical organometallics such as dialkylzinc, Grignard reagents, and trialkylaluminum have been developed [2][3][4][5][6][7][8][9]. Recently, also Cu-catalyzed conjugate additions of organozirconium [10][11] or

• organoboron reagents were realized [12]. Also, in terms of suitable Michael acceptors as substrates, unsaturated ketones, aldehydes, esters, thioesters, amides, alkenyl heterocycles and enoyl heterocycles became viable for conjugate additions. The maturity and robustness of this methodology is documented by

Enolates ambushed – asymmetric tandem conjugate addition and subsequent enolate trapping with conventional and less traditional electrophiles

• Péter Kisszékelyi and
• Radovan Šebesta

Beilstein J. Org. Chem. 2023, 19, 593–634, doi:10.3762/bjoc.19.44

• organic synthetic transformations. Chiral metal enolates obtained by asymmetric conjugate additions of organometallic reagents are structurally complex intermediates that can be employed in many transformations. In this review, we describe this burgeoning field that is reaching maturity after more than 25

• array of organic synthetic transformations. Enolates are usually formed by deprotonation of the corresponding organic compound. However, other synthetic approaches for their generation exist, such as cleavage of enol ethers and esters, halogen–metal exchange, transmetalations, and conjugate additions to

• were successfully employed in asymmetric conjugate additions (ACA) [3][4][5][6][7][8][9], mainly organozinc [10], Grignard [11][12][13], trialkylaluminum [14], or organozirconium reagents [15]. Additions with these reagents lead to corresponding zinc, magnesium, aluminum, and zirconium enolates, which

An accelerated Rauhut–Currier dimerization enabled the synthesis of (±)-incarvilleatone and anticancer studies

• Tharun K. Kotammagari,
• Sweta Misra,
• Sayantan Paul,
• Sunita Kunte,
• Rajesh G. Gonnade,
• Manas K. Santra and
• Asish K. Bhattacharya

Beilstein J. Org. Chem. 2023, 19, 204–211, doi:10.3762/bjoc.19.19

• intermolecular fashion to form a C–C bond between the two Michael acceptors. This whole process involves two intermolecular conjugate additions, which leads to low reactivity. In case of intramolecular RC reactions, a high reactivity is observed. This is due to one intermolecular and one intramolecular conjugate

New advances in asymmetric organocatalysis

• Radovan Šebesta

Beilstein J. Org. Chem. 2022, 18, 240–242, doi:10.3762/bjoc.18.28

• possibilities in combination of covalent and noncovalent activation, our group designed and synthesized N-sulfinylpyrrolidine-containing ureas and thioureas and applied them in Michael additions of aldehydes to heterocycle containing nitroalkenes [25]. Dubey and Chowdhury showed that 1,4-conjugate additions of

Highly stereocontrolled total synthesis of racemic codonopsinol B through isoxazolidine-4,5-diol vinylation

• Lukáš Ďurina,
• Anna Ďurinová,
• František Trejtnar,
• Ľuboš Janotka,
• Lucia Messingerová,
• Jana Doháňošová,
• Ján Moncol and
• Róbert Fischer

Beilstein J. Org. Chem. 2021, 17, 2781–2786, doi:10.3762/bjoc.17.188

• the proline catalysis are of higher purity (after purification by silica gel column chromatography), than those synthesized by other methods [16]. Definitely, the effective asymmetric organocatalytic conjugate additions of hydroxylamines to enals using various catalysts provide access to

Recent advances in the asymmetric phosphoric acid-catalyzed synthesis of axially chiral compounds

• Alemayehu Gashaw Woldegiorgis and
• Xufeng Lin

Beilstein J. Org. Chem. 2021, 17, 2729–2764, doi:10.3762/bjoc.17.185

• (4H)-ones to β,γ-alkynyl-α-imino esters. Synthesis of chiral tetrasubstituted allenes and naphthopyrans. Asymmetric remote 1,8-conjugate additions

Solvent-free synthesis of enantioenriched β-silyl nitroalkanes under organocatalytic conditions

• Akhil K. Dubey and
• Raghunath Chowdhury

Beilstein J. Org. Chem. 2021, 17, 2642–2649, doi:10.3762/bjoc.17.177

• the best of our knowledge, organocatalyzed or metal-catalyzed enantioselective conjugate additions of nitroalkanes to β-silyl enones are not yet known. Results and Discussion The optimization study began with the conjugate addition reaction between β-TMS enone 1a and nitromethane (2) as the model

Electron-rich triarylphosphines as nucleophilic catalysts for oxa-Michael reactions

• Susanne M. Fischer,
• Simon Renner,
• A. Daniel Boese and
• Christian Slugovc

Beilstein J. Org. Chem. 2021, 17, 1689–1697, doi:10.3762/bjoc.17.117

• , triarylphosphines are generally less reactive in conjugate additions than trialkylphosphines and often high catalyst loadings of up to 20 mol % and elevated temperatures are necessary to obtain satisfactory conversions [5][14][15]. The low reactivity of arylphosphines can be enhanced by introducing electron

Methodologies for the synthesis of quaternary carbon centers via hydroalkylation of unactivated olefins: twenty years of advances

• Thiago S. Silva and
• Fernando Coelho

Beilstein J. Org. Chem. 2021, 17, 1565–1590, doi:10.3762/bjoc.17.112

• obtained exclusively as the trans diastereoisomer (Scheme 26B). Based on the previous work using the Fe(III)/silane system to promote hydrogen atom transfer to olefins, the Xu group explored the use of unsaturated imines 70 as radical acceptors in MHAT-driven radical conjugate additions with olefins [94

A comprehensive review of flow chemistry techniques tailored to the flavours and fragrances industries

• Guido Gambacorta,
• James S. Sharley and
• Ian R. Baxendale

Beilstein J. Org. Chem. 2021, 17, 1181–1312, doi:10.3762/bjoc.17.90

Recent advances in palladium-catalysed asymmetric 1,4–additions of arylboronic acids to conjugated enones and chromones

• Jan Bartáček,
• Jan Svoboda,
• Martin Kocúrik,
• Jaroslav Pochobradský,
• Alexander Čegan,
• Miloš Sedlák and
• Jiří Váňa

Beilstein J. Org. Chem. 2021, 17, 1048–1085, doi:10.3762/bjoc.17.84

• excellent both in terms of enantioselectivities and conversions (up to 98%; up to 83% ee; Table 28). The reuse of the heterogeneous catalyst has not been studied in this case. In 2020, our group reported the first heterogeneous polystyrene-supported recyclable catalyst for the asymmetric conjugate additions

Copper-catalysed alkylation of heterocyclic acceptors with organometallic reagents

• Yafei Guo and
• Syuzanna R. Harutyunyan

Beilstein J. Org. Chem. 2020, 16, 1006–1021, doi:10.3762/bjoc.16.90

• enantioselectivity have been reported for conjugate additions of both organoaluminium and organozinc reagents, these reagents also present major drawbacks, namely their commercial availability and atom efficiency, given that only one alkyl group is transferred from the organometallic reagent to the Michael acceptor

Recent advances in Cu-catalyzed C(sp³)–Si and C(sp³)–B bond formation

• Balaram S. Takale,
• Ruchita R. Thakore,
• Elham Etemadi-Davan and
• Bruce H. Lipshutz

Beilstein J. Org. Chem. 2020, 16, 691–737, doi:10.3762/bjoc.16.67

• scope of this silicon addition to unsaturated lactones using copper catalysis together with NHC ligand L16. The ligand used previously to great advantage by the Hoveyda and Oestreich groups for conjugate additions did not yield high ees for these substrates. The authors designed a new NHC possessing

• adducts (e.g., 373 to form products, 374 and 375; Scheme 59) highlights the utility of this methodology [109]. Following Hoveyda’s report on enantioselective Cu-catalyzed conjugate additions of borylated butadiene, generated in situ, to enolates [110], Procter et al. described the regio-divergent

Copper-catalyzed enantioselective conjugate addition of organometallic reagents to challenging Michael acceptors

• Delphine Pichon,
• Jennifer Morvan,
• Christophe Crévisy and
• Marc Mauduit

Beilstein J. Org. Chem. 2020, 16, 212–232, doi:10.3762/bjoc.16.24

• -acyloxazolidinones, N-acylpyrrolidinones, amides, and N-acylpyrroles have been scarcely investigated in Cu ECA despite their usefulness for postfunctionalizations. This tutorial review aims to describe the early examples and recent advances in copper-catalyzed asymmetric conjugate additions of dialkylzinc, Grignard

• a higher reactivity in conjugate additions, even with the less reactive MeMgBr. As depicted in Scheme 6, excellent yields and remarkable enantioselectivities (up to 96%) were obtained in ECAs of linear aliphatic Grignard reagents (in particular MeMgBr) to a wide range of substrates, catalyzed by

• ]. Indeed, due to their poor reactivity compared to other Michael acceptors, catalytic asymmetric conjugate additions of organometallic reagents to N,N-dialkylenamides remained a real challenge. However, thanks to the synergistic action of the boron-based Lewis acid BF3∙Et2O, CuBr∙SMe2, and the chiral (R,S

Combination of multicomponent KA² and Pauson–Khand reactions: short synthesis of spirocyclic pyrrolocyclopentenones

• Riccardo Innocenti,
• Elena Lenci,
• Gloria Menchi and
• Andrea Trabocchi

Beilstein J. Org. Chem. 2020, 16, 200–211, doi:10.3762/bjoc.16.23

• the equatorial alcohol, although in lower yield. The use of CeCl3 together with EtMgBr was found particularly effective to suppress conjugate additions, with similar yield as reported for analogous substrates [56]. Subsequent acid-catalyzed displacement of the hydroxy moiety with aniline in the

N-(1-Phenylethyl)aziridine-2-carboxylate esters in the synthesis of biologically relevant compounds

• Iwona E. Głowacka,
• Aleksandra Trocha,
• Andrzej E. Wróblewski and
• Dorota G. Piotrowska

Beilstein J. Org. Chem. 2019, 15, 1722–1757, doi:10.3762/bjoc.15.168

• transition state was involved. Acid-induced aziridine ring openings and subsequent conjugate additions to the α,β-unsaturated lactone led to the formation of cis-fused [5,5']bicyclic compounds 186a or 186b. Reduction of the lactone moiety in 186a and subsequent deprotection gave (2S,3R,4S,5R)-184. In order

Intramolecular cascade annulation triggered by rhodium(III)-catalyzed sequential C(sp²)–H activation and C(sp³)–H amination

• Liangliang Song,
• Guilong Tian,
• Johan Van der Eycken and
• Erik V. Van der Eycken

Beilstein J. Org. Chem. 2019, 15, 571–576, doi:10.3762/bjoc.15.52

• polymerization, prone to go through conjugate additions [11][12]. Moreover, the cyclometalation intermediates are unstable, and the β-substitution or α,β-disubstitution of acrylate sterically prevents the cyclometalation [13][14]. Despite these, several approaches have been developed to synthesize pyridones and

Cobalt- and rhodium-catalyzed carboxylation using carbon dioxide as the C1 source

• Tetsuaki Fujihara and
• Yasushi Tsuji

Beilstein J. Org. Chem. 2018, 14, 2435–2460, doi:10.3762/bjoc.14.221

• carboxylation of mesityl triflate (5) at 40 °C proceeded successfully, affording 6 in 77% yield (Scheme 6) Carboxylation of α,β-unsaturated nitriles and esters α,β-Unsaturated carbonyl compounds are good substrates for conjugate additions that use a catalytic amount of a metal complex and a stoichiometric

Asymmetric Michael addition reactions catalyzed by calix[4]thiourea cyclohexanediamine derivatives

• Zheng-Yi Li,
• Hong-Xiao Tong,
• Yuan Chen,
• Hong-Kui Su,
• Tangxin Xiao,
• Xiao-Qiang Sun and
• Leyong Wang

Beilstein J. Org. Chem. 2018, 14, 1901–1907, doi:10.3762/bjoc.14.164

• also synthesized a model catalyst 4 by a similar synthetic procedure as outlined for catalyst 2. All compounds 1–4 were fully characterized by NMR spectroscopy and HRMS analyses. Optimization of reaction conditions Generally, conjugate additions were employed for evaluating the catalytic activities of

Conjugate addition–enantioselective protonation reactions

• James P. Phelan and
• Jonathan A. Ellman

Beilstein J. Org. Chem. 2016, 12, 1203–1228, doi:10.3762/bjoc.12.116

• synthetic manipulations. Furthermore, enantioselective conjugate additions to α-amino-α,β-unsaturated esters provides rapid access to enantioenriched α-amino acid derivatives. However, α,β-unsaturated esters present some challenges; the transient enolate intermediate can adopt E- or Z-enolate geometries

• . Building on his asymmetric conjugate additions to α-substituted enones, Luo demonstrated that Hantzsch ester 133 chemoselectively reduces activated alkenes 132 in the presence of α-substituted vinyl ketones 118, generating carbon nucleophiles 135 in situ. These nucleophiles then reacted with the α

A modular approach to neutral P,N-ligands: synthesis and coordination chemistry

• Vladislav Vasilenko,
• Torsten Roth,
• Clemens K. Blasius,
• Sebastian N. Intorp,
• Hubert Wadepohl and
• Lutz H. Gade

Beilstein J. Org. Chem. 2016, 12, 846–853, doi:10.3762/bjoc.12.83

• hydrogenations [1][2] and allylic substitutions [3][4] to Heck reactions [5] and conjugate additions to enones [6]. Their popularity arises from the inherent electronic disparity of the phosphorus and the nitrogen donor groups, rendering one binding site a soft π-acceptor featuring a pronounced trans effect and

Cupreines and cupreidines: an established class of bifunctional cinchona organocatalysts

• Laura A. Bryant,
• Rossana Fanelli and
• Alexander J. A. Cobb

Beilstein J. Org. Chem. 2016, 12, 429–443, doi:10.3762/bjoc.12.46

• then turn to asymmetric 1,2-additions followed by conjugate additions, a cyclopropanation, (ep)oxidations, α-functionalisation processes, cycloadditions, domino processes and finally miscellaneous reactions. We ultimately aim to demonstrate through this plethora of diverse processes, that the 6’-OH

• stereochemical outcome of the reaction [36]. This work was based on a related scheme from Chimni and co-worker, who used CPN derivatised at the 9-OH with 1-naphthoyl in the addition of sesamol to a range of N-sulfonylimines [37]. 1,4-Conjugate additions Deng and co-workers have contributed many examples of 1,4