Synthesis of fluorinated acid-functionalized, electron-rich nickel porphyrins

• Mike Brockmann,
• Jonas Lobbel,
• Lara Unterriker and
• Rainer Herges

Beilstein J. Org. Chem. 2024, 20, 2954–2958, doi:10.3762/bjoc.20.248

• favor an alternating sequence of the chains pointing upward and downward. Conclusion This study reports the synthesis of perfluoroalkyl carboxylic esters with CH2–OTf groups in the ω-position of the type TfO–CH2–(CF2)n–COOCH3 (n = 2, 4, 6, Tf = triflate). The latter compounds were used in Williamson

A review of recent advances in electrochemical and photoelectrochemical late-stage functionalization classified by anodic oxidation, cathodic reduction, and paired electrolysis

• Nian Li,
• Ruzal Sitdikov,
• Ajit Prabhakar Kale,
• Joost Steverlynck,
• Bo Li and
• Magnus Rueping

Beilstein J. Org. Chem. 2024, 20, 2500–2566, doi:10.3762/bjoc.20.214

Carbonylative synthesis and functionalization of indoles

• Alex De Salvo,
• Raffaella Mancuso and
• Xiao-Feng Wu

Beilstein J. Org. Chem. 2024, 20, 973–1000, doi:10.3762/bjoc.20.87

• ., in two different periods, reported two paradigmatic examples for indole syntheses. In 2010, they developed the synthesis of 1-(alkoxyarylmethyl)indole-3-carboxylic esters from 2-alkynylaniline imines by using PdI2/KI as catalyst system and oxygen as oxidant [15]. In particular, the reaction was

• years later, they performed, using the same catalytic and oxidative conditions, another oxidative heterocyclization/alkoxycarbonylation process for the synthesis of N-substituted indole-3-carboxylic esters and N–H free indole-3-carboxylic esters from N-substituted 2-alkynylanilines and 2-alkynylanilines

• the formation of N-substituted indole derivatives from N-substituted anilines. The direct PdI2/KI oxidative carbonylation of 2-alkynylanilines does not lead to the formation of indole-3-carboxylic esters but to the formation of acyclic carbamates. For this reason, they performed the reaction in the

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

• -workers [61] extended the application of NHC–copper catalysts to the conjugate addition of boronates to acyclic α,β-unsaturated carboxylic esters, ketones, and thioesters leading to the enantioselective formation of boron-substituted quaternary carbon stereogenic centers (Scheme 43). All transformations

Derivatives of benzo-1,4-thiazine-3-carboxylic acid and the corresponding amino acid conjugates

• Péter Kisszékelyi,
• Tibor Peňaška,
• Klára Stankovianska,
• Mária Mečiarová and
• Radovan Šebesta

Beilstein J. Org. Chem. 2022, 18, 1195–1202, doi:10.3762/bjoc.18.124

• isolated products were not the expected 4H-, rather the 2H-benzo-1,4-thiazines. 3D renderings of derivatives 19a and 19b obtained at the ωB97xD/6-31G* level are depicted in Scheme 5b. Conclusion In conclusion, we have described the synthesis of rarely explored 4H-benzo[b][1,4]thiazine-3-carboxylic esters

1,2-Naphthoquinone-4-sulfonic acid salts in organic synthesis

• Ruan Carlos B. Ribeiro,
• Patricia G. Ferreira,
• Amanda de A. Borges,
• Luana da S. M. Forezi,
• Fernando de Carvalho da Silva and
• Vitor F. Ferreira

Beilstein J. Org. Chem. 2022, 18, 53–69, doi:10.3762/bjoc.18.5

• enzyme human carboxylesterase (hCE1) that cleaves carboxylic esters. This enzyme functions in the detoxification metabolism of carcinogenic and mutagenic organic compounds, converting them into nontoxic metabolites. This compound served as inspiration for Hatfield and co-workers [84], who proposed the

Synthesis of trifluoromethyl ketones by nucleophilic trifluoromethylation of esters under a fluoroform/KHMDS/triglyme system

• Yamato Fujihira,
• Yumeng Liang,
• Makoto Ono,
• Kazuki Hirano,
• Takumi Kagawa and
• Norio Shibata

Beilstein J. Org. Chem. 2021, 17, 431–438, doi:10.3762/bjoc.17.39

• with the optimized conditions in hand (entry 9, Table 1). Various carboxylic esters were investigated in the presence of 1.1 equiv of HCF3 and two equiv of KHMDS (Scheme 3). Methyl 2-naphthoate (1a) gave 2a in 75% yield, but sterically demanding methyl 1-naphthoate (1b) gave the desired trifluoromethyl

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

• corresponding amides 4a–d by treatment with phosphorus decasulfide (Scheme 1). It is worth noting that amides of 1-alkyl-1,2,3-triazole-4-carboxylic acids are poorly represented in the literature and the methods of their preparation require the addition of alkyl azides to acetylene carboxylic esters and

Synthesis of (macro)heterocycles by consecutive/repetitive isocyanide-based multicomponent reactions

• Angélica de Fátima S. Barreto and
• Carlos Kleber Z. Andrade

Beilstein J. Org. Chem. 2019, 15, 906–930, doi:10.3762/bjoc.15.88

• isocyanide-based multicomponent reactions in the synthesis of macrocycles containing a tetrazole nucleus [30]. The strategy was based on the use of α-isocyano-ω-carboxylic esters 71 via a microwave-mediated Ugi-azide reaction at the beginning of the synthesis and an intramolecular Ugi reaction of

5-Aminopyrazole as precursor in design and synthesis of fused pyrazoloazines

• Ranjana Aggarwal and
• Suresh Kumar

Beilstein J. Org. Chem. 2018, 14, 203–242, doi:10.3762/bjoc.14.15

• (5H)-one derivatives 204 by refluxing in 1 N sodium hydroxide. Pyrazolo[3,4-d]pyrimidinone 204 were further chlorinated by phosphorus oxychloride and subsequently converted to carboxylic esters 207 via cyanation followed by hydrolysis and esterification. Kaplan et al. [20] explored the synthesis of

Phosphonic acid: preparation and applications

• Charlotte M. Sevrain,
• Mathieu Berchel,
• Hélène Couthon and
• Paul-Alain Jaffrès

Beilstein J. Org. Chem. 2017, 13, 2186–2213, doi:10.3762/bjoc.13.219

• . Nevertheless, G. David et al. have reported in a study dedicated to the synthesis of methacrylate monomers functionalized with phosphonic acids the occurrence of side compounds [199]. The treatment of the bis-phosphonate 72 with TMS-Br followed by methanolysis, induces a cleavage of the carboxylic esters

Synthesis of γ-hydroxypropyl P-chirogenic (±)-phosphorus oxide derivatives by regioselective ring-opening of oxaphospholane 2-oxide precursors

• Iris Binyamin,
• Shoval Meidan-Shani and
• Nissan Ashkenazi

Beilstein J. Org. Chem. 2015, 11, 1332–1339, doi:10.3762/bjoc.11.143

• new P(V)-carbon bond(s) [12]. While the former synthetic approach has been studied extensively and its scope and limitations are well documented, the full potential of the latter approach may be regarded as only partially exploited. Similar to Grignard reactions with carboxylic esters, the formation

A Lewis acid-promoted Pinner reaction

• Dominik Pfaff,
• Gregor Nemecek and
• Joachim Podlech

Beilstein J. Org. Chem. 2013, 9, 1572–1577, doi:10.3762/bjoc.9.179

• Dominik Pfaff Gregor Nemecek Joachim Podlech Institut für Organische Chemie, Karlsruher Institut für Technologie (KIT), Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany 10.3762/bjoc.9.179 Abstract Carbonitriles and alcohols react in a Lewis acid-promoted Pinner reaction to carboxylic esters. Best

• activated nitrilium cation, which can be attacked by the alcohol component. Proton transfer (P.T.) yields the imidate hydrochloride [3]. Various transformations are possible with the imidate hydrochlorides: Hydrolysis at low pH leads to carboxylic esters, where basic hydrolysis yields imidates. Reaction

• electron-rich benzyl alcohol, furnished no carboxylic ester at all (Table 2, entry 15). Rather poor yields of the respective carboxylic esters were achieved, when unsubstituted benzyl alcohol (56) or 4-fluorobenzyl alcohol (64) were reacted with one of the carbonitriles (Table 3). Instead we isolated

Use of 3-[¹⁸F]fluoropropanesulfonyl chloride as a prosthetic agent for the radiolabelling of amines: Investigation of precursor molecules, labelling conditions and enzymatic stability of the corresponding sulfonamides

• Reik Löser,
• Steffen Fischer,
• Achim Hiller,
• Martin Köckerling,
• Uta Funke,
• Aurélie Maisonial,
• Peter Brust and
• Jörg Steinbach

Beilstein J. Org. Chem. 2013, 9, 1002–1011, doi:10.3762/bjoc.9.115

• -labelled sulfonyl chloride [18F]10 with 4-nitroaniline, potassium trimethylsilanolate was tested as auxiliary base. This reagent has good solubility in organic solvents and was suggested by Laganis and Chenard as equivalent for the O2− ion and is typically used to convert carboxylic esters to the

A facile, rapid, one-pot regio/stereoselective synthesis of 2-iminothiazolidin-4-ones under solvent/scavenger-free conditions

• Murugan Sathishkumar,
• Sangaraiah Nagarajan,
• Poovan Shanmugavelan,
• Murugan Dinesh and
• Alagusundaram Ponnuswamy

Beilstein J. Org. Chem. 2013, 9, 689–697, doi:10.3762/bjoc.9.78

• halides [16][17] or carboxylic esters [18]. These protocols are generally solution phase methods using organic solvents and acid scavengers. In the present scenario, such protocols may not be recommended by the principles of green chemistry. Consequently, the search for simple and efficient

Presence or absence of a novel charge-transfer complex in the base-catalyzed hydrolysis of N-ethylbenzamide or ethyl benzoate

• Shinichi Yamabe,
• Wei Guan and
• Shigeyoshi Sakaki

Beilstein J. Org. Chem. 2013, 9, 185–196, doi:10.3762/bjoc.9.22

• dilute alkali is the usual way of hydrolyzing esters, and the reaction is called saponification. The base-catalyzed hydrolysis of amides is an important model for the enzymatic cleavage of peptide bonds [2][3]. The base-promoted hydrolyses of carboxylic esters and amides accompanying the 18O exchange

Regioselective ester cleavage during the preparation of bisphosphonate methacrylate monomers

• Kamel Chougrani,
• Gilles Niel,
• Bernard Boutevin and
• Ghislain David

Beilstein J. Org. Chem. 2011, 7, 364–368, doi:10.3762/bjoc.7.46

• influence of the chain length between the methacrylate and acetate groups. It is worth mentioning that the phosphonic acid 7a is stable in the two-step deprotection process (Table 1, entry 7) emphasizing the greater stability of conjugated carboxylic esters over unconjugated ones. Other examples of similar

N-alkyl-N-(phosphonoethyl) substituted (meth)acrylamides – new adhesive monomers for self-etching self-priming one part dental adhesive

• Joachim E. Klee and
• Uwe Lehmann

Beilstein J. Org. Chem. 2009, 5, No. 72, doi:10.3762/bjoc.5.72

• spectroscopy as well as refractive index and viscosity. The phosphonoethyl substituted (meth)acrylamide monomers show improved hydrolytic stability compared to carboxylic esters. The highest stability was found for the phosphonoethyl substituted acrylamide monomers. Acrylamides have a larger polymerization

• behavior and the relatively high molecular weight are responsible for the lower adhesion. Conclusion A series of novel N-alkyl-N-(phosphonoethyl) substituted mono-, bis- and tris(meth)acrylamides 3 was synthesized which shows improved hydrolytic stability compared to carboxylic esters. Their stability

The Elbs and Boyland- Sims peroxydisulfate oxidations

• E. J. Behrman

Beilstein J. Org. Chem. 2006, 2, No. 22, doi:10.1186/1860-5397-2-22

• the intermediate sulfate esters using acetic acid which spares carboxylic esters. These authors also give a current example of the use of sulfate esters as a protecting group in synthesis [7] as do Bunnett and Jenvey. [8] Parenthetically, there is a disputed report of the formation of quinones in low