Anomeric 1,2,3-triazole-linked sialic acid derivatives show selective inhibition towards a bacterial neuraminidase over a trypanosome trans-sialidase

• Peterson de Andrade,
• Sanaz Ahmadipour and
• Robert A. Field

Beilstein J. Org. Chem. 2022, 18, 208–216, doi:10.3762/bjoc.18.24

• natural substrate for sialidases and its chemical modification has been a useful approach to generate potent and selective inhibitors. Aiming at advancing the discovery of selective Trypanosoma cruzi trans-sialidase (TcTS) inhibitors, we have synthesised a small series of anomeric 1,2,3-triazole-linked

• differences in sialidases that need to be addressed in order to achieve selective inhibition. Keywords: inhibition; neuraminidase; sialic acid; trans-sialidase; 1,2,3-triazole; Introduction Amongst the diversity of glycans present in living organisms, N-acetylneuraminic acid (Neu5Ac, sialic acid) is

• series of C-2-modified sialic acid bearing a monosaccharide tethered via 1,2,3-triazole ring (sialylmimetic neoglycoconjugates) [19] that showed 67–91% inhibitory activity at 1 mM. We now envisaged replacing the monosaccharide moiety by (hetero)aromatic substituents (Figure 2A) expecting better

Synthesis and antimicrobial activity of 1H-1,2,3-triazole and carboxylate analogues of metronidazole

• Satya Kumar Avula,
• Syed Raza Shah,
• Khdija Al-Hosni,
• Muhammad U. Anwar,
• Rene Csuk,
• Biswanath Das and
• Ahmed Al-Harrasi

Beilstein J. Org. Chem. 2021, 17, 2377–2384, doi:10.3762/bjoc.17.154

• -Wittenberg, Kurt-Mothes-Str. 2, d-06120, Halle (Saale), Germany 10.3762/bjoc.17.154 Abstract Herein, a series of novel 1H-1,2,3-triazole and carboxylate derivatives of metronidazole (5a–i and 7a–e) were synthesized and evaluated for their antimicrobial activity in vitro. All the newly synthesized compounds

• inhibiting effects compared to the activity of the parent compound. Amongst the tested compounds 5b, 5c, 5e, 7b and 7e displayed excellent potent antimicrobial activity. The current study has demonstrated the usefulness of the 1H-1,2,3-triazole moiety in the metronidazole skeleton. Keywords: antimicrobial

• agents; carboxylate analogues; 1H-1,2,3-triazole analogues; metronidazole; synthesis; Introduction Metronidazole (1) is an important antimicrobial agent which has been clinically used successfully for a long time. It was originally used for the treatment of infections caused by Trichomonas varginalis

(Phenylamino)pyrimidine-1,2,3-triazole derivatives as analogs of imatinib: searching for novel compounds against chronic myeloid leukemia

• Luiz Claudio Ferreira Pimentel,
• Lucas Villas Boas Hoelz,
• Henayle Fernandes Canzian,
• Frederico Silva Castelo Branco,
• Andressa Paula de Oliveira,
• Vinicius Rangel Campos,
• Floriano Paes Silva Júnior,
• Rafael Ferreira Dantas,
• Jackson Antônio Lamounier Camargos Resende,
• Anna Claudia Cunha,
• Nubia Boechat and
• Mônica Macedo Bastos

Beilstein J. Org. Chem. 2021, 17, 2260–2269, doi:10.3762/bjoc.17.144

• )pyrimidine-pyridine (PAPP) group as a pharmacophoric fragment, and these compounds were biologically evaluated. The synthesis of twelve new compounds was performed in three steps and assisted by microwave irradiation in a 1,3-dipolar cycloaddition to obtain 1,2,3-triazole derivatives substituted on carbon C

• in the docking studies. Keywords: chronic myeloid leukemia; 1,3-dipolar cycloaddition; imatinib; (phenylamino)pyrimidine-pyridine; 1,2,3-triazole; Introduction Changes in tyrosine kinase proteins (TKPs), either by mutation or chromosomal translocation, can turn them into potent oncogenes

• analogs [12][13], in this work, we designed a series of imatinib 1,2,3-triazole analogs 1a,b and 2a–j (Figure 1). The 1,2,3-triazoles are heterocyclic compounds, consisting of a five-membered ring, containing two carbon atoms and three nitrogen atoms [14]. The application of click chemistry, a concept

A recent overview on the synthesis of 1,4,5-trisubstituted 1,2,3-triazoles

• Pezhman Shiri,
• Ali Mohammad Amani and
• Thomas Mayer-Gall

Beilstein J. Org. Chem. 2021, 17, 1600–1628, doi:10.3762/bjoc.17.114

• synthesis of a wide variety of relevant 1,4,5-trisubstituted 1,2,3-triazole molecules are reported. The synthesis of this category of diverse fully functionalized 1,2,3-triazoles has become a necessary and unique research subject in modern synthetic organic key transformations in academia, pharmacy, and

• -triazoles; N-containing heterocycles; 1,4,5-trisubstituted 1,2,3-triazoles; Introduction A high number of N-heterocycles [1][2][3][4] are identified, and this number is increasing very quickly [5][6][7][8]. Among them, the small heterocyclic ring of the 1,2,3-triazole is present in a broad variety of

• compounds with not only biological but also industrial significance [9][10][11]. It possesses a cyclic scaffold with carbon and three nitrogen elements in the ring [12][13][14][15]. An immense versatility of biological properties is possessed by 1,2,3‐triazole heterocyclic systems, and many strategies are

Double-headed nucleosides: Synthesis and applications

• Vineet Verma,
• Jyotirmoy Maity,
• Vipin K. Maikhuri,
• Ritika Sharma,
• Himal K. Ganguly and
• Ashok K. Prasad

Beilstein J. Org. Chem. 2021, 17, 1392–1439, doi:10.3762/bjoc.17.98

• . The heterocyclic structures which were found to be attached to these double-headed nucleosides include triazolophthalazine [11], 4,6-di-tert-butylbenzoxazole [12], mesitylisoxazole [13], 5-trimethylsilyl-1,2,3-triazole [14], 1-pivaloyloxymethyl-1H-1,2,3-triazole [15], 1,3,4-oxadiazino[6,5-b]indole [16

• ]. Nielsen and co-workers [43] synthesized 2′-(4-(thymin-1-ylmethyl)-1,2,3-triazole-1-yl)- and 2′-(4-(N6-benzoyladenine-9-ylmethyl)-1,2,3-triazole-1-yl)-substituted double-headed nucleosides of 2′-deoxy-5′-O-(4,4′-dimethoxytrityl)uridine (14 and 15) from the nucleoside azide 12 which in turn was obtained by

• complementary bases [34]. Nielsen and co-workers [23] synthesized the double-headed nucleoside 1-(5′-O-(4,4′-dimethoxytrityl)-2′-C-((4-(pyren-1-yl)-1,2,3-triazole-1-yl)methyl)arabinofuranosyl)uracil (41) starting from spironucleoside 2 which in turn was synthesized from uridine following a procedure reported in

Microwave-assisted multicomponent reactions in heterocyclic chemistry and mechanistic aspects

• Shivani Gulati,
• Stephy Elza John and
• Nagula Shankaraiah

Beilstein J. Org. Chem. 2021, 17, 819–865, doi:10.3762/bjoc.17.71

Synthesis of β-triazolylenones via metal-free desulfonylative alkylation of N-tosyl-1,2,3-triazoles

• Soumyaranjan Pati,
• Renata G. Almeida,
• Eufrânio N. da Silva Júnior and
• Irishi N. N. Namboothiri

Beilstein J. Org. Chem. 2021, 17, 762–770, doi:10.3762/bjoc.17.66

• 61% yields, respectively. The reaction of mild electron withdrawing 3-methoxyphenyl-1,2,3-triazole 1e led to product 3h in low yield (38%) whereas the corresponding 4-tert-butylphenyl-1,2,3-triazole 1f afforded the product 3i in 53% yield. Later, the reaction was performed using various

• the scope of cyclohexane-1,3-dione 2a is limited. On the contrary, dimedone (2d) did not react with N-tosyl-1,2,3-triazole, but reacted with N-mesyl-1,2,3-triazole to form the 5,5-dimethyl-3-oxo-cyclohex-1-en-1-yl methanesulfonate intermediate 4a. The highly substrate-dependent nature of the reaction

• excellent yields. Nucleophilic addition to 5- and 6-membered cyclic tosyloxyenones. Synthesis, functionalization and applications of triazoles. The reaction was performed using 0.2 mmol N-tosyl-1,2,3-triazole 1 and 0.2 mmol of cyclohexyl-1,3-dione 2. Yields are determined after silica gel column

Effective microwave-assisted approach to 1,2,3-triazolobenzodiazepinones via tandem Ugi reaction/catalyst-free intramolecular azide–alkyne cycloaddition

• Maryna O. Mazur,
• Oleksii S. Zhelavskyi,
• Eugene M. Zviagin,
• Svitlana V. Shishkina,
• Vladimir I. Musatov,
• Maksim A. Kolosov,
• Elena H. Shvets,
• Anna Yu. Andryushchenko and
• Valentyn A. Chebanov

Beilstein J. Org. Chem. 2021, 17, 678–687, doi:10.3762/bjoc.17.57

• into two well-resolved doublets and two triplets slightly shifted downfield. This phenomenon can be explained by the loss of conformational motion of the aromatic ring and the formation of the hard molecular carcass of the 7-membered ring fused with a 1,2,3-triazole cycle. Then we applied higher

Deoxygenative C2-heteroarylation of quinoline N-oxides: facile access to α-triazolylquinolines

• Geetanjali S. Sontakke,
• Rahul K. Shukla and
• Chandra M. R. Volla

Beilstein J. Org. Chem. 2021, 17, 485–493, doi:10.3762/bjoc.17.42

• reaction conditions (Scheme 1b) [58][59][60][61][62]. Results and Discussion We initiated our trials employing easily accessible quinoline N-oxide (1a) and 1-tosyl-4-phenyl-1,2,3-triazole (2a) as model substrates. Subjecting the reaction mixture to 100 °C in the presence of DIPEA in 1,2-dichloroetane (DCE

• ) with 4-phenyl-1-tosyl-1H-1,2,3-triazole (2a, 8.3 mmol, 1.2 equiv) at room temperature for 1 h, the reaction worked equally well and produced the desired product 3a in 87% yield (1.6 g). In addition, to enlarge the simplicity of the developed protocol for selective C2-triazolylation of quinoline

• the stepwise pathway. The plausible mechanism for the C2-triazolylation of quinoline N-oxides is presented in Scheme 7 [64]. The reaction initiates by the nucleophilic attack of quinoline N-oxide, e.g., 1a, on the sulfonyl group of N-sulfonyl-1,2,3-triazole 2, leading to the formation of intermediate

1,2,3-Triazoles as leaving groups in S_NAr–Arbuzov reactions: synthesis of C6-phosphonated purine derivatives

• Kārlis-Ēriks Kriķis,
• Irina Novosjolova,
• Anatoly Mishnev and
• Māris Turks

Beilstein J. Org. Chem. 2021, 17, 193–202, doi:10.3762/bjoc.17.19

• leaving group in SNAr reactions with S- and N-nucleophiles [19][20][21]. It is worth to note that 2/6-amino-6/2-triazolylpurines possess high levels of fluorescence [19][22][23][24]. Herein, we describe an extension for SNAr reactions that makes use of the 1,2,3-triazole leaving group of 2,6

• a mixture of hexane and DCM using the slow-evaporation technique (Figure 2). This follows the previously reported regioselective C6-substitution of 2,6-bistriazolylpurines in SNAr transformations. Conclusion We have developed a novel SNAr–Arbuzov transformation that makes use of 1,2,3-triazole as a

• C16H27ClN4O3P, 389.1504; found, 389.1508. General procedure for the synthesis of 9-alkyl-2,6-bistriazolyl-9H-purine derivatives 6 Dimethyl 1,1'-(9-heptyl-9H-purine-2,6-diyl)bis(1H-1,2,3-triazole-4-carboxylate) (6a): CuI (0.06 g, 0.30 mmol, 0.12 equiv) was added to a stirred solution of 2,6-diazido-9-heptyl-9H

Regioselective synthesis of heterocyclic N-sulfonyl amidines from heteroaromatic thioamides and sulfonyl azides

• Vladimir Ilkin,
• Vera Berseneva,
• Tetyana Beryozkina,
• Tatiana Glukhareva,
• Lidia Dianova,
• Wim Dehaen,
• Eugenia Seliverstova and
• Vasiliy Bakulev

Beilstein J. Org. Chem. 2020, 16, 2937–2947, doi:10.3762/bjoc.16.243

• , Department of Chemistry, KU Leuven, Celestijnenlaan 200F, 3001 Leuven, Belgium 10.3762/bjoc.16.243 Abstract N-Sulfonyl amidines bearing 1,2,3-triazole, isoxazole, thiazole and pyridine substituents were successfully prepared for the first time by reactions of primary, secondary and tertiary heterocyclic

• thioamides with alkyl- and arylsulfonyl azides. For each type of thioamides a reliable procedure to prepare N-sulfonyl amidines in good yields was found. Reactions of 1-aryl-1,2,3-triazole-4-carbothioamides with azides were shown to be accompanied with a Dimroth rearrangement to form 1-unsubstituted 5

• -arylamino-1,2,3-triazole-4-N-sulfonylcarbimidamides. 2,5-Dithiocarbamoylpyridine reacts with sulfonyl azides to form a pyridine bearing two sulfonyl amidine groups. Keywords: amidines; Dimroth rearrangement; isoxazoles; sulfonyl thiazoles; thioamides; 1,2,3-triazoles; Introduction The biological activity

Azidophosphonium salt-directed chemoselective synthesis of (E)/(Z)-cinnamyl-1H-triazoles and regiospecific access to bromomethylcoumarins from Morita–Baylis–Hillman adducts

• Soundararajan Karthikeyan,
• Radha Krishnan Shobana,
• Kamarajapurathu Raju Subimol,
• J. Helen Ratna Monica and
• Ayyanoth Karthik Krishna Kumar

Beilstein J. Org. Chem. 2020, 16, 1579–1587, doi:10.3762/bjoc.16.130

• transformations for complex molecules [29][30][31]. Two individual research groups have reported the multistep pathway to access the cinnamyl-1H-1,2,3-triazole derivatives IX from acetates of MBH adducts (Scheme 2) [32][33]. The other preferable moiety for triazole transformations is the allyl halide of MBH

• equiv) and CuI (3 mol %) at room temperature. To our expectations, the reaction afforded the (E)-cinnamyl-1H-1,2,3-triazole in a low yield of 24% (Table 1, entry 1). Thereby, we anticipated that an increase in the proportion of the AzPS would substantially increase the yield of 3a (Table 1, entries 2

• efficiency of this reaction. The substrate scope of the optimized reaction and its limitations were further extended to structurally distinct MBH adducts (Scheme 3). The MBH adducts derived from methoxy and ethoxy acrylate stereochemically afforded the (E)-cinnamyl-1,4-disubstituted 1,2,3-triazole

Photocatalysis with organic dyes: facile access to reactive intermediates for synthesis

• Stephanie G. E. Amos,
• Marion Garreau,
• Luca Buzzetti and
• Jerome Waser

Beilstein J. Org. Chem. 2020, 16, 1163–1187, doi:10.3762/bjoc.16.103

A systematic review on silica-, carbon-, and magnetic materials-supported copper species as efficient heterogeneous nanocatalysts in “click” reactions

• Pezhman Shiri and
• Jasem Aboonajmi

Beilstein J. Org. Chem. 2020, 16, 551–586, doi:10.3762/bjoc.16.52

• groups. The intramolecular reaction of an alkyne as a dipolarophile with an azide as a 1,3-dipole to produce the desired 1,2,3-triazole motif is a model of “click” chemistry. The concept of “click” chemistry is an idiom that was developed by Sharpless and Meldal and later by others to describe organic

• reaction proceeds under mild conditions, is effective, efficient, and requires no column purification in many cases. The Cu alkyne–azide cycloaddition (CuAAC) version also gives only 1,2,3-triazole products substituted at the 1- and 4-positions in an aqueous medium even at room temperature and requires no

• 1,2,3-triazole products substituted at the 1- and 5-positions [13]. A range of copper(I) species (copper(I) iodide, copper(I) bromide, [Cu(CH3CN)4]PF6, (EtO)3P⋅CuI, and [Cu(PPh3)3]Br) has been applied in the prementioned reaction [14]. Generally, Cu(I) species are not thermodynamically stable and can be

Aerobic synthesis of N-sulfonylamidines mediated by N-heterocyclic carbene copper(I) catalysts

• Faïma Lazreg,
• Marie Vasseur,
• Alexandra M. Z. Slawin and
• Catherine S. J. Cazin

Beilstein J. Org. Chem. 2020, 16, 482–491, doi:10.3762/bjoc.16.43

• diphenylamine, only 20% of the desired product was observed (12c). Interestingly, with benzyl azide, a substrate not containing a sulfonyl moiety, the product obtained is the 1,2,3-triazole derivative [33], resulting from a [3 + 2] cycloaddition of azide and alkyne (Scheme 6). The catalytic system was also

Halogen-bonding-induced diverse aggregation of 4,5-diiodo-1,2,3-triazolium salts with different anions

• Xingyu Xu,
• Shiqing Huang,
• Zengyu Zhang,
• Lei Cao and
• Xiaoyu Yan

Beilstein J. Org. Chem. 2020, 16, 78–87, doi:10.3762/bjoc.16.10

• chemistry, anion recognition, organocatalysis, materials science and tuning of biomolecular systems [17][18][19][20][21][22][23][24][25][26][27]. 1,2,3-Triazole-based XB-donors, such as 5-iodo-1,2,3-triazoles A [28][29][30][31][32][33] and 5-iodo-1,2,3-triazolium B [34][35][36][37] (Figure 1), are promising

• aldehydes [44]. Despite a variety of XB donors based on 1,2,3-triazole have been reported, no 4,5-diido-1,2,3-triazolium salts have been reported for an XB interaction. Herein, we report the synthesis and characterization of 4,5-diido-1,2,3-triazolium D with different anions. The crystal structures of these

• understand the 1,2,3-triazole based XB donors, model 1,2,3-triazole A, 1,2,3-triazolium B, 1,2,3-triazolylidene complex C-CuI and diiodotriazolium D were calculated by DFT calculations (Figure 9). The calculation results show that σ holes in diiodotriazolium D are mainly located in the elongation of two C–I

Diversity-oriented synthesis of spirothiazolidinediones and their biological evaluation

• Sambasivarao Kotha,
• Gaddamedi Sreevani,
• Lilya U. Dzhemileva,
• Milyausha M. Yunusbaeva,
• Usein M. Dzhemilev and
• Vladimir A. D’yakonov

Beilstein J. Org. Chem. 2019, 15, 2774–2781, doi:10.3762/bjoc.15.269

• represent an important class of nitrogen-containing biologically active compounds which exhibit various biological properties, such as antiviral, antibacterial and anticancer, etc. [55][56][57][58]. Recently, the use of 1,2,3-triazole derivatives as drug candidates has been increased for clinical therapy of

Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization

• Valentina A. Ol’shevskaya,
• Elena G. Kononova and
• Andrei V. Zaitsev

Beilstein J. Org. Chem. 2019, 15, 2704–2709, doi:10.3762/bjoc.15.263

• 1,2,3-triazole heterocycles via the copper-catalyzed azide–alkyne cycloaddition reaction (CuAAC) between alkynes and azides, developed independently by Sharpless [41] and Meldal [42]. In addition to the applications of triazoles as pharmacophores in the potential biologically active molecules, these

• -propargylmaleimide [44] was carried out successfully in CH2Cl2 and the fluorinated porphyrin–triazole–maleimide conjugates 7a and 7b were obtained in 54–58% yield. In these conjugates the tetrafluorophenyl units of the porphyrin macrocycle where separated from maleimides with 1,2,3-triazole spacer groups. Removal of

Click chemistry towards thermally reversible photochromic 4,5-bisthiazolyl-1,2,3-triazoles

• Chenxia Zhang,
• Kaori Morinaka,
• Mahmut Kose,
• Takashi Ubukata and
• Yasushi Yokoyama

Beilstein J. Org. Chem. 2019, 15, 2161–2169, doi:10.3762/bjoc.15.213

• AcOEt than in toluene, and the thermal back reaction rate in AcOEt was increased. Conclusion We have synthesized three novel thermally reversible 4,4'-(1-benzyl-1H-1,2,3-triazole-4,5-diyl)bis(5-methyl-2-(4-substituted-phenyl)thiazole)s 1o–3o by Ru(I)-catalysed Huisgen cyclization, which is a type of

1,2,3-Triazolium macrocycles in supramolecular chemistry

• Mastaneh Safarnejad Shad,
• Pulikkal Veettil Santhini and
• Wim Dehaen

Beilstein J. Org. Chem. 2019, 15, 2142–2155, doi:10.3762/bjoc.15.211

• candidates for amide bond surrogates. Interestingly, 1,2,3-triazole units can act as sensors for both anions and cations via different binding mechanisms [16][17]. The heterocyclic ring N2 and N3 atoms could realize the selective recognition of the cations whereas the C5–H···anions electrostatic interaction

• of 1,4-disubstituted 1,2,3- triazole units [19][20][21][22][23][24]. Macrocyclic ring closure can be achieved by the CuAAC of building blocks functionalized with both azide and alkyne, using [1 + 1], [2 + 2], [n + n] strategies depending on how much triazoles are needed to be included in the

• happen between Lewis bases and electron-defective heavy chalcogen atoms containing Lewis acidic s-holes which is known under the term chalcogen bonding (ChB) [18]. A mechanically interlocked rotaxane 8 (Figure 8) has been prepared by Beer and co-workers utilizing the 5-(methylchalcogeno)-1,2,3-triazole

Attempted synthesis of a meta-metalated calix[4]arene

• Christopher D. Jurisch and
• Gareth E. Arnott

Beilstein J. Org. Chem. 2019, 15, 1996–2002, doi:10.3762/bjoc.15.195

• yielding transformations to azide and 1,2,3-triazole derivatives which may have application in other areas of research. Keywords: calixarene; inherent chirality; mesoionic carbene; mononitration; ruthenacycle; Introduction Calix[4]arenes are a class of diverse macrocyclic compounds which have been the

• Ullmann-type coupling to give aryl azide 2, which readily reacted with phenylacetylene in a copper-catalyzed Huisgen 1,3-dipolar cycloaddition to give 1,2,3-triazole 3 (Scheme 1). The formation of the ruthenacycle was then achieved using Albrecht’s method involving regioselective methylation of triazole 3

Polyaminoazide mixtures for the synthesis of pH-responsive calixarene nanosponges

• Antonella Di Vincenzo,
• Antonio Palumbo Piccionello,
• Alberto Spinella,
• Delia Chillura Martino,
• Marco Russo and
• Paolo Lo Meo

Beilstein J. Org. Chem. 2019, 15, 633–641, doi:10.3762/bjoc.15.59

• azide stretching of the reticulating agent, respectively. On the other hand, a tiny signal at 3140 cm−1 appears, which can be attributed to the Csp2–H stretching typical of the newly formed 1,2,3-triazole ring. The occurrence of the triazole ring is also accounted for by tiny signals at 1244, 1204, 1050

Copper(I)-catalyzed tandem reaction: synthesis of 1,4-disubstituted 1,2,3-triazoles from alkyl diacyl peroxides, azidotrimethylsilane, and alkynes

• Muhammad Israr,
• Changqing Ye,
• Munira Taj Muhammad,
• Yajun Li and
• Hongli Bao

Beilstein J. Org. Chem. 2018, 14, 2916–2922, doi:10.3762/bjoc.14.270

• available lauroyl peroxide (2a), and TMSN3 (Table 1). In a preliminary experiment, the reaction of 1a with 2a in the presence of 10 mol % of CuCl in THF at 50 °C afforded 1,4-disubstituted 1,2,3-triazole 3a in 65% isolated yield (Table 1, entry 1). Surprisingly, under these conditions no CuAAC product

Assembly of fully substituted triazolochromenes via a novel multicomponent reaction or mechanochemical synthesis

• Robby Vroemans,
• Yenthel Verhaegen,
• My Tran Thi Dieu and
• Wim Dehaen

Beilstein J. Org. Chem. 2018, 14, 2689–2697, doi:10.3762/bjoc.14.246

• , which enables them to undergo a high variety of reactions and functionalizations [15]. Combining the chromene core with the 1,2,3-triazole structural motif has led to some interesting new molecules [16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31]. Very recently, spiro-fused

• ], via intramolecular cyclization of a diazomethane group and a nitrile [23], or via our recently reported NH-triazole synthesis starting from 6-methoxyflavanone [24]. Furthermore, 1,4,5-trisubstituted 1,2,3-triazole annulated chromenes have been reported via an intramolecular arylation reaction of 1,2,3

• substituents on the chromene core and 1,2,3-triazole offer a lot of possibilities for further derivatization and optimization towards biologically relevant structures such as flavonoid structures. Our group developed a Knoevenagel-assisted three-component reaction of (protected) salicylaldehyde, ethyl

Catalyst-free synthesis of 4-acyl-NH-1,2,3-triazoles by water-mediated cycloaddition reactions of enaminones and tosyl azide

• Lu Yang,
• Yuwei Wu,
• Yiming Yang,
• Chengping Wen and
• Jie-Ping Wan

Beilstein J. Org. Chem. 2018, 14, 2348–2353, doi:10.3762/bjoc.14.210

• , authentically mild conditions (40 °C stirring) as well as practical scalability. Keywords: additive-free; catalyst-free; cycloaddition; enaminones; on water; 1,2,3-triazole; Introduction Discovering sustainable chemical syntheses constitutes one central issue of modern organic chemistry. A large number of

• , including those reactions involving valuable C–C [7][8][9][10][11], C–heteroatom [12][13][14][15][16], heteroatom–heteroatom [17][18] bond formation as well as divergent cascade reactions [19][20][21][22][23], are presently taking place to guide the progress of sustainable organic synthesis. 1,2,3-Triazole

• development of these metal-catalyzed cycloaddition strategies [33][34][35]. Alongside the vast progress happened in MAAC-based 1,2,3-triazole synthesis, the past decade has witnessed the emergence of another powerful cycloaddition tool for the 1,2,3-triazole synthesis: the metal-free cycloaddition of azides