Iridium-catalyzed hydroacylation reactions of C1-substituted oxabenzonorbornadienes with salicylaldehyde: an experimental and computational study

• Angel Ho,
• Austin Pounder,
• Krish Valluru,
• Leanne D. Chen and
• William Tam

Beilstein J. Org. Chem. 2022, 18, 251–261, doi:10.3762/bjoc.18.30

• -stereocontrolled ring-opening reactions of oxa- and azabicyclic olefins with dialkylzinc reagents catalyzed by a nickel compound (Scheme 1) [60]. The reaction was entirely stereoselective; however, unsymmetrical OBDs 5 produced mixtures of regioisomers 6 and 7. In the same year, Hill and co-workers published a

• reaction (Scheme 2). Satisfyingly, the reaction exclusively afforded the C3-hydroacylated regioisomer 15 in all cases. Moreover, the reaction was stereoselective for the formation of the exo-adduct rather than a mixture of endo/exo products as previously reported by Tanaka/Suemune [65] and Bolm [66], who

Synthesis and late stage modifications of Cyl derivatives

• Phil Servatius and
• Uli Kazmaier

Beilstein J. Org. Chem. 2022, 18, 174–181, doi:10.3762/bjoc.18.19

• decided to take advantage of an asymmetric chelate enolate Claisen rearrangement, which should allow the stereoselective generation of the unusual amino acid, depending on the configuration of the chiral allylic alcohol used [41][42]. If a peptide Claisen rearrangement [43][44][45] is carried out with a

The enzyme mechanism of patchoulol synthase

• Houchao Xu,
• Bernd Goldfuss,
• Gregor Schnakenburg and
• Jeroen S. Dickschat

Beilstein J. Org. Chem. 2022, 18, 13–24, doi:10.3762/bjoc.18.2

• in the structure of 3 with the absolute configuration as shown in Figure 2. The absolute configuration of 3 was furthermore independently confirmed through a stereoselective deuteration strategy (Scheme 4; all labelling experiments of this study are summarised in Supporting Information File 1, Table

• stereoselective labelling experiments using (E)-(4-13C,4-2H)IPP (blue H = 2H) and (Z)-(4-13C,4-2H)IPP (red H = 2H), and (R)-(1-13C,1-2H)IPP (blue H = 2H) and (S)-(1-13C,1-2H)IPP (red H = 2H). Black dots indicate 13C-labelled carbons. Labelling experiments on the biosynthesis of patchoulol (3, part 1). Black dots

First total synthesis of hoshinoamide A

• Haipin Zhou,
• Zihan Rui,
• Yiming Yang,
• Shengtao Xu,
• Yutian Shao and
• Long Liu

Beilstein J. Org. Chem. 2021, 17, 2924–2931, doi:10.3762/bjoc.17.201

• synthesized in high efficiency. After systematic screening of the coupling reagents in liquid phase, the key intermediate tripeptide 7 was obtained in high yield. The solid-phase synthesis improves the entire efficiency of the synthetic route. This strategy could be applied to the stereoselective synthesis of

Total synthesis of the O-antigen repeating unit of Providencia stuartii O49 serotype through linear and one-pot assemblies

• Tanmoy Halder and
• Somnath Yadav

Beilstein J. Org. Chem. 2021, 17, 2915–2921, doi:10.3762/bjoc.17.199

• stereoselective glycosylations. The work provides an access to the trisaccharide repeating unit of the O-polysaccharide of Providencia stuartii O49 with the stereospecific α-p-methoxyphenyl glycoside. Structure of the repeating unit of the lipopolysaccharide of Providencia stuartii O49 serotype. Retrosynthetic

Iron-catalyzed domino coupling reactions of π-systems

• Austin Pounder and
• William Tam

Beilstein J. Org. Chem. 2021, 17, 2848–2893, doi:10.3762/bjoc.17.196

The PIFA-initiated oxidative cyclization of 2-(3-butenyl)quinazolin-4(3H)-ones – an efficient approach to 1-(hydroxymethyl)-2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones

• Alla I. Vaskevych,
• Nataliia O. Savinchuk,
• Ruslan I. Vaskevych,
• Eduard B. Rusanov,
• Oleksandr O. Grygorenko and
• Mykhailo V. Vovk

Beilstein J. Org. Chem. 2021, 17, 2787–2794, doi:10.3762/bjoc.17.189

• well as by Sm(OTf)3-catalyzed stereoselective [3 + 2] cycloaddition of bis-silyldienediolate and imines, in turn synthesized from anthranylamides and benzaldehydes [32]. A promising approach to the synthesis of 2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-one derivatives substituted at the pyrrolidine

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

• -stereoselective epoxidation of 2,3-dihydroisoxazole with in situ-generated DMDO, the syn-selective α-chelation-controlled addition of vinyl-MgBr/CeCl3 to the isoxazolidine-4,5-diol intermediate, and the substrate-directed epoxidation of the terminal double bond of the corresponding γ-amino-α,β-diol with aqueous

• first prepared synthetically before its isolation from natural crude material, employing a stereoselective addition of an aryl Grignard reagent to a five-membered chiral cyclic nitrone derived from ᴅ-arabinose [2]. Its analytical data were consistent with those for the later isolated natural product

• methodology based on the trans-stereoselective epoxidation reaction of 2,3-dihydroisoxazoles followed by the regioselective hydrolysis of the corresponding isoxazolidinyl epoxide [15][16]. Very recently, we have reported the synthesis of γ-(hydroxyamino)-α,β-diols by the addition of Grignard reagents 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

• acids are widely used in stereoselective oxidative/cross-coupling of two aryl counterparts, asymmetric control of aromatic ring formation, atroposelective functionalization of biaryl compounds, and so on [17][29][30]. In this context, Akiyama (2004) described that chiral phosphoric acids (CPAs) have

• regio- and stereoselective γ-addition reaction of isoxazol-5(4H)-ones 103 to β,γ-alkynyl-α-imino esters 102 for the synthesis of axially chiral tetrasubstituted α-amino allenoates 104 containing an adjacent quaternary carbon stereocenter and an axially chiral tetrasubstituted allene scaffold [104

• -naphthylamines with azodicarboxylates. Synthesis of brominated atropisomeric N-arylquinoids. The enantioselective syntheses of axially chiral SPINOL derivatives. γ-Addition reaction of various 2,3-disubstituted indoles to β,γ-alkynyl-α-imino esters. Regio- and stereoselective γ-addition reactions of isoxazol-5

Synthetic strategies toward 1,3-oxathiolane nucleoside analogues

• Umesh P. Aher,
• Dhananjai Srivastava,
• Girij P. Singh and
• Jayashree B. S

Beilstein J. Org. Chem. 2021, 17, 2680–2715, doi:10.3762/bjoc.17.182

• -oxathiolane ring with different nucleobases in a way that only one isomer is produced in a stereoselective manner via N-glycosylation. An emphasis has been placed on the C–N-glycosidic bond constructed during the formation of the nucleoside analogue. The third focus is on the separation of enantiomers of 1,3

• , ii) a stereoselective N-glycosylation process that is compatible with an enantiomerically pure substrate, and iii) separation of enantiomers by chemical or enzymatic resolution methods. This review summarizes the methods used to synthesize 1,3-oxathiolane nucleosides. Many methods provide the

• effective enantiopure synthesis of lamivudine (1) were achieved by many scientists. The synthesis of 1,3-oxathiolane nucleosides utilizing stereoselective coupling of a nucleobase with the oxathiolane sugar intermediate via in situ chelation was reported by Liotta and co-workers (Scheme 29) [72

AlBr₃-Promoted stereoselective anti-hydroarylation of the acetylene bond in 3-arylpropynenitriles by electron-rich arenes: synthesis of 3,3-diarylpropenenitriles

• Yelizaveta Gorbunova,
• Dmitry S. Ryabukhin and
• Aleksander V. Vasilyev

Beilstein J. Org. Chem. 2021, 17, 2663–2667, doi:10.3762/bjoc.17.180

• , benzene and its polymethylated derivatives) under the action of aluminum bromide (AlBr3, 6 equiv) at room temperature for 0.5–2 h result in the stereoselective formation of 3,3-diarylpropenenitriles (Ar(Ar′)C=CHCN) in yields of 20–64%, as products of mainly anti-hydroarylation of the acetylene bond. The

• nitriles 1. At the last step of the reaction, a proton substitutes AlBr3, and final hydrolysis of the reaction mixture gives rise to nitriles 2. It should be noted that this AlBr3-promoted hydroarylation of acetylene nitriles 1 (Scheme 1) is a novel transition-metal (Pd, Pt, Rh, etc.)-free stereoselective

• [17]. Conclusion We have developed a novel transition-metal (Pd, Pt, Rh, etc.)-free procedure for the regio- and stereoselective hydroarylation of the carbon–carbon triple bond in 3-arylpropynenitriles by arenes under electrophilic activation by aluminum bromide AlBr3. The obtained 3,3

Ligand-dependent stereoselective Suzuki–Miyaura cross-coupling reactions of β-enamido triflates

• Tomáš Chvojka,
• Athanasios Markos,
• Svatava Voltrová,
• Radek Pohl and
• Petr Beier

Beilstein J. Org. Chem. 2021, 17, 2657–2662, doi:10.3762/bjoc.17.179

• 43 Prague 2, Czech Republic 10.3762/bjoc.17.179 Abstract The stereoselective Suzuki–Miyaura cross-coupling of (Z)-β-enamido triflates is demonstrated. Depending on the nature of the ligand in the palladium catalyst, either retention or inversion of the configuration during the synthesis of β,β

• of cytotoxic, antifungal, or antibiotic properties [10][11][12]. Modern stereoselective syntheses leading to highly substituted enamides include cross-coupling of vinyl (pseudo)halides or organoboron compounds [13], hydroamidation of alkynes [14][15][16], ynamide functionalization [17][18][19], or

• isomerization of N-allyl amides [20], but still possess drawbacks, especially for stereoselective synthesis of tri- and tetrasubstituted enamides. Recently, we have reported a triflic acid-mediated reaction of N-fluoroalkyl-1,2,3-triazoles leading to (Z)-β-enamido triflates [21] and Lewis acid-mediated reaction

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

• Enantioenriched organosilanes are attractive molecules in organic synthesis owing to their potential applications in stereoselective synthesis [1][2]. The unique sterical and electronical features of the C–Si bond can induce stereodifferentiation at the adjacent prostereogenic center in organic transformations [2

N-Sulfinylpyrrolidine-containing ureas and thioureas as bifunctional organocatalysts

• Viera Poláčková,
• Dominika Krištofíková,
• Boglárka Némethová,
• Renata Górová,
• Mária Mečiarová and
• Radovan Šebesta

Beilstein J. Org. Chem. 2021, 17, 2629–2641, doi:10.3762/bjoc.17.176

• a privileged structural motif central to many catalyst designs [12]. This fact stems from the success of diarylprolinol silyl ethers as chiral organocatalysts, which were independently introduced by Hayashi [13] and Jørgensen [14]. These compounds were used in a large number of stereoselective

• -Butanesulfinamide is highly useful in stereoselective synthesis as a stereoinducing group [21]. Thus, N-sulfinylureas and thioureas are a new class of organocatalysts, with the sulfinyl group acting both as an acidifying and a chiral controlling moiety. A variety of N-sulfinylureas catalyzed aza-Henry reaction

Recent advances in organocatalytic asymmetric aza-Michael reactions of amines and amides

• Pratibha Sharma,
• Raakhi Gupta and
• Raj K. Bansal

Beilstein J. Org. Chem. 2021, 17, 2585–2610, doi:10.3762/bjoc.17.173

• -MRs, each highlighting a certain aspect of the reaction. While Sánchez-Roselló et al. [18] classified these reactions on the basis of the nature of the substrates, Nayak et al. [19] and Bhanja et al. [20] focused on the stereoselective synthesis of nitrogen heterocycles via Michael cascade reactions

• . Recently, Vinogradov et al. [21] reviewed the synthesis of pharmacology-relevant nitrogen heterocycles via stereoselective aza-MRs. On the other hand, Enders et al. [22], Wang et al. [23] as well as Krishna et al. [24] highlighted the scope and catalytic performances of some organocatalysts in asymmetric

• . Review In the present review, the known stereoselective syntheses of pharmacology-oriented nitrogen containing heterocyclic scaffolds via non-covalent bonding and covalent bonding organocatalytic aza-MRs has been systematized. This classification is especially useful for researchers to understand both

Visible-light-mediated copper photocatalysis for organic syntheses

• Yajing Zhang,
• Qian Wang,
• Zongsheng Yan,
• Donglai Ma and
• Yuguang Zheng

Beilstein J. Org. Chem. 2021, 17, 2520–2542, doi:10.3762/bjoc.17.169

• study [41][42] in 2017. This metal-catalyzed, photoinduced, and asymmetric radical transformation requires two catalysts, namely, (i) a metal catalyst that promotes electron transfer and (ii) a separate chiral catalyst that facilitates the highly stereoselective bond formation. In 2016, Fu [82

• subsequent stereoselective transformations. In addition, Fimognari’s group [101] utilized copper photoredox catalysts to achieve the N-desulfonylation of benzenesulfonyl-protected N-heterocycles 72 (Scheme 29). In 2019, Xiao’s group [102] observed that under visible light or copper catalysis, cycloketone

• applications of photoinduced copper-catalyzed reactions include alkene/alkyne functionalization, organic halide functionalization, and alkyl C–H functionalization. This review introduced the photoinduced copper-catalyzed stereoselective reactions within these broad reaction categories. Copper salts coordinate

Strategies for the synthesis of brevipolides

• Yudhi D. Kurniawan and
• A'liyatur Rosyidah

Beilstein J. Org. Chem. 2021, 17, 2399–2416, doi:10.3762/bjoc.17.157

• reduced in a stereoselective manner adopting Luche conditions to provide diol 24 (dr 97:3), which after masking the primary alcohol moiety as a silyl ether, allowed isolation of the desired product 25 in 86% yield. This intermediate possessed the correct chirality on the free secondary alcohol to

• stereoselective reduction (Scheme 8). Among a selection of reagents, Mohapatra found that lithium tri-tert-butoxyaluminum hydride in ethanol at low temperature furnished 71 as a single diastereoisomer in 94% yield. The allylic alcohol moiety was protected as TBDPS ether 73 (92%) and oxidatively cleaved following

• ). The olefin moieties can be installed via stereoselective allylation and cinnamic acid esterification of 94, which is derived from symmetrical alcohol 95. The right-hand side portion of this molecule can be constructed by epoxidation of the allylic alcohol derived from α,β-unsaturated ester 96 and the

Advances in mercury(II)-salt-mediated cyclization reactions of unsaturated bonds

• Sumana Mandal,
• Raju D. Chaudhari and
• Goutam Biswas

Beilstein J. Org. Chem. 2021, 17, 2348–2376, doi:10.3762/bjoc.17.153

• with Hg(OAc)2 affording the corresponding cyclized pyanosylmethylmercuric chloride derivatives 12 (Scheme 5). This methodology can be used to synthesize rare C-glycosyl carbohydrates from easily available sugars. In a similar manner, stereoselective cyclization of C-glycosyl amino acid derivative 13

• using mercuric trifluoroacetate Hg(TFA)2 at room temperature was performed. The reaction proceeds primarily through stereoselective cyclization to give α-ᴅ-C-glycopyranosyl amino acid derivative 14 as the major product [43]. Nevertheless, C-mannopyranosyl derivatives cannot be achieved in a similar

• of Hg(OAc)2 [53]. The cyclized products 34A,B formed from starting material 33 were regiospecific and followed Markovnikoff’s type addition in the reaction [54][55][56][57]. It was also reported that the formation of α-phosphorylated pyrrolidines mostly takes place in regio- and stereoselective ways

Halides as versatile anions in asymmetric anion-binding organocatalysis

• Lukas Schifferer,
• Martin Stinglhamer,
• Kirandeep Kaur and
• Olga García Macheño

Beilstein J. Org. Chem. 2021, 17, 2270–2286, doi:10.3762/bjoc.17.145

• step by chloride abstraction that leads to the formation of an oxocarbenium intermediate, which then undergoes the stereoselective addition of the nucleophile. Mechanistic insights revealed that two thiourea molecules are, in fact, needed and cooperatively participate in the activation of 73. However

Photoredox catalysis in nickel-catalyzed C–H functionalization

• Lusina Mantry,
• Rajaram Maayuri,
• Vikash Kumar and
• Parthasarathy Gandeepan

Beilstein J. Org. Chem. 2021, 17, 2209–2259, doi:10.3762/bjoc.17.143

• transformations have become one of the most reliable and basic tools for designing and manufacturing biologically relevant molecules and functional materials [1][2][3][4]. The formation of highly chemo-, regio-, and stereoselective products with excellent yields is the key reason for transition-metal catalysis as

Transition-metal-free intramolecular Friedel–Crafts reaction by alkene activation: A method for the synthesis of some novel xanthene derivatives

• Tülay Yıldız,
• İrem Baştaş and
• Hatice Başpınar Küçük

Beilstein J. Org. Chem. 2021, 17, 2203–2208, doi:10.3762/bjoc.17.142

• method using π-activated alcohols has frequently been used for xanthene synthesis. Some of these methods are the stereoselective synthesis of 9-vinyl-substituted unsymmetrical xanthenes and thioxanthenes by intramolecular FCA reaction [39], Lewis acid-catalyzed intramolecular FCA [40], and the synthesis

Progress and challenges in the synthesis of sequence controlled polysaccharides

• Giulio Fittolani,
• Theodore Tyrikos-Ergas,
• Denisa Vargová,
• Manishkumar A. Chaube and
• Martina Delbianco

Beilstein J. Org. Chem. 2021, 17, 1981–2025, doi:10.3762/bjoc.17.129

• group on the glycosyl donor and the acceptor for the stereoselective formation of the β(1–3) linkage (Figure 4) [132]. Interestingly, oligomers bearing several 4,6-O-benzylidene groups show anomalously small coupling constants for some of the C-1 hydrogens. NMR [133] and X-ray [134] studies revealed

• linkages is particularly relevant, as α(1–4)-glucans form the backbone of starch, with the linear amylose and the branched amylopectin, and α(1–3)-glucans are related to fungal pathogenicity in plants [168]. Only few options can aid the stereoselective construction of 1,2-cis glycosidic bonds. In general

• -mediated aglycon delivery (BMAD) with the use of a diboron catalyst allowed for regio-, as well as stereoselective glycosylation to achieve an α(1-3)-pentaglucoside [175]. Regioselective 1,2-cis-glycosylation could also be achieved by boron-catalyzed coupling via a SNi-type mechanism [176]. Hydrogen bond

Asymmetric organocatalyzed synthesis of coumarin derivatives

• Natália M. Moreira,
• Lorena S. R. Martelli and
• Arlene G. Corrêa

Beilstein J. Org. Chem. 2021, 17, 1952–1980, doi:10.3762/bjoc.17.128

• acid (4) as catalyst [30]. Based on this pioneer work, our research group described an efficient, highly stereoselective, one-pot process comprising an organocatalytic conjugate addition of dimedone or 4-hydroxycoumarin 1 to α,β-unsaturated aldehydes 2 followed by an intramolecular isocyanide-based

• stereoselective one-pot procedure for the synthesis of five-membered annulated coumarins 28 was described by the group of Enders [40]. Using dual catalysis, with a cinchona primary amine derivative 22 and silver carbonate, a series of functionalized coumarin derivatives 28 were obtained in good yields (up to 91

• synthesis of 3,4-dihydrocoumarins 80 bearing a cyclohexene ring, through [4 + 2] cycloaddition between 2,4-dienals 79 and 3-coumarincarboxylates 43. This stereoselective transformation was performed using a squaramide 81 derivative catalyst, which activates the aldehyde with the formation of an enamine

On the application of 3d metals for C–H activation toward bioactive compounds: The key step for the synthesis of silver bullets

• Renato L. Carvalho,
• Amanda S. de Miranda,
• Mateus P. Nunes,
• Roberto S. Gomes,
• Guilherme A. M. Jardim and
• Eufrânio N. da Silva Júnior

Beilstein J. Org. Chem. 2021, 17, 1849–1938, doi:10.3762/bjoc.17.126

Breaking paracyclophane: the unexpected formation of non-symmetric disubstituted nitro[2.2]metaparacyclophanes

• Suraj Patel,
• Tyson N. Dais,
• Paul G. Plieger and
• Gareth J. Rowlands

Beilstein J. Org. Chem. 2021, 17, 1518–1526, doi:10.3762/bjoc.17.109

• mixture of starting material 6, the conjugate addition product 14, and a trace of the denitration product 15. The structure of both compounds was confirmed by single X-ray crystallography (Figure 4 and Figure 5). The addition of methanol is stereoselective with only a single diastereomer of 14 being