Radical ligand transfer: a general strategy for radical functionalization

• David T. Nemoto Jr,
• Kang-Jie Bian,
• Shih-Chieh Kao and
• Julian G. West

Beilstein J. Org. Chem. 2023, 19, 1225–1233, doi:10.3762/bjoc.19.90

• simplified manganese salen complex I, allowing for the identity of the carbon–heteroatom bond to be controlled based on added nucleophile and enabling C–Cl, C–N, and C–S bonds to be formed directly while completely suppressing traditional ATRA products [9]. In mechanistic studies, rearrangement products

Strategies in the synthesis of dibenzo[b,f]heteropines

• David I. H. Maier,
• Barend C. B. Bezuidenhoudt and
• Charlene Marais

Beilstein J. Org. Chem. 2023, 19, 700–718, doi:10.3762/bjoc.19.51

• etherification entails the palladium or copper-catalysed formation of a carbon–heteroatom bond. Despite significant successes and facile access to the core tricyclic motif, access to dibenzo[b,f]heteropines with disparately substituted aromatic rings fused to the heterocyclic ring and varied substitution

DDQ in mechanochemical C–N coupling reactions

• Shyamal Kanti Bera,
• Rosalin Bhanja and
• Prasenjit Mal

Beilstein J. Org. Chem. 2022, 18, 639–646, doi:10.3762/bjoc.18.64

• moiety in 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), it was well established as a hydride transfer reagent in various organic reactions [14][15]. Generally, DDQ assists in dehydrogenation reactions in organic synthesis [16]. In this context, various carbon–heteroatom bond formation reactions such

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

• discussed. Recent methods in the pursuit for efficient and economical carbon–carbon and carbon–heteroatom bond-forming reactions, such as cross-coupling, CDC, and oxidative coupling/difunctionalizations, will be summarized. The review is categorized by reaction type, and the type of bonds being formed. For

• –heteroatom bond-forming reactions. Catalysis, as a synthetic tool, is widely employed to accomplish transformations to produce many various pharmaceuticals, polymeric materials, and fine chemicals [1][2][3][4][5][6][7][8]. Catalysis is one of the fundamental pillars of green chemistry, the design of chemical

• the design of novel domino reactions. Keywords: cascade; catalysis; coupling; earth-abundant; iron; Introduction Over the past couple decades, the use of transition-metal-catalyzed cross-coupling reactions have become a staple within the organic chemist’s arsenal of carbon–carbon and carbon

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

• catalysts for a variety of enantioselective transformations, especially for carbon–carbon and carbon–heteroatom bond-forming reactions [15][28]. They are important for the development of axially chiral compounds, which are involved in the design of chiral catalysts and ligands. Currently, chiral phosphoric

Synthetic approaches to bowl-shaped π-conjugated sumanene and its congeners

• Shakeel Alvi and
• Rashid Ali

Beilstein J. Org. Chem. 2020, 16, 2212–2259, doi:10.3762/bjoc.16.186

• molecules. Notably, it has been found that the introduction of heteroatom(s) in the periphery of these architectures generally decrease the depth of bowl, may be because of an increase in the carbon–heteroatom bond length. For this reason, these heterobuckybowls possess less strained energy due to shallower

Chlorination of phenylallene derivatives with 1-chloro-1,2-benziodoxol-3-one: synthesis of vicinal-dichlorides and chlorodienes

• Zhensheng Zhao and
• Graham K. Murphy

Beilstein J. Org. Chem. 2018, 14, 796–802, doi:10.3762/bjoc.14.67

• - and vinyl chlorides are highly sought-after intermediates for effecting allylations, and for use in transition metal-catalyzed carbon–carbon and carbon–heteroatom bond-forming reactions [13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28]. Given the versatility of allyl chloride and β

Recent advances in copper-catalyzed asymmetric coupling reactions

• Fengtao Zhou and
• Qian Cai

Beilstein J. Org. Chem. 2015, 11, 2600–2615, doi:10.3762/bjoc.11.280

• construction of heteroatom-containing ring systems. This review summarizes the recent progress in copper-catalyzed asymmetric coupling reactions for the formation of C–C and carbon–heteroatom bonds. Keywords: asymmetric; carbon–heteroatom bond; copper; coupling; Introduction Copper-mediated coupling

• ). Copper-catalyzed couplings of allylic halides with nucleophiles Transition metal-catalyzed allylic substitutions are the most important process for carbon–carbon and carbon–heteroatom bond formation in organic synthesis [56][57][58]. Allylic substitution of the substrate with nucleophiles can afford two

Chiral phosphines in nucleophilic organocatalysis

• Yumei Xiao,
• Zhanhu Sun,
• Hongchao Guo and
• Ohyun Kwon

Beilstein J. Org. Chem. 2014, 10, 2089–2121, doi:10.3762/bjoc.10.218

• of carbon–carbon and carbon–heteroatom bond-forming transformations [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18]. Many phosphine-catalyzed reactions have been developed for the syntheses of various biologically important acyclic and cyclic molecules. Asymmetric variants of these

Photorelease of phosphates: Mild methods for protecting phosphate derivatives

• Sanjeewa N. Senadheera,
• Abraham L. Yousef and
• Richard S. Givens

Beilstein J. Org. Chem. 2014, 10, 2038–2054, doi:10.3762/bjoc.10.212

• organic chemistry and biochemistry, but they are particularly important for mechanistic studies in biochemistry and biophysics [6][8][9][10][11]. Most PPG candidates require sufficiently high energy excited states for heterolysis of a carbon–oxygen or carbon–heteroatom bond that binds the chromophore to a

Transition-metal and organocatalysis in natural product synthesis

• David Yu-Kai Chen and
• Dawei Ma

Beilstein J. Org. Chem. 2013, 9, 1192–1193, doi:10.3762/bjoc.9.134

• the history of chemical science. These transformations, largely concerning carbon–carbon/carbon–heteroatom bond formations, asymmetric induction, and catalysis, constantly expand the repertoire of powerful tools available at the organic chemist’s disposal, and enable more challenging synthetic

Cascade radical reaction of substrates with a carbon–carbon triple bond as a radical acceptor

• Hideto Miyabe,
• Ryuta Asada and
• Yoshiji Takemoto

Beilstein J. Org. Chem. 2013, 9, 1148–1155, doi:10.3762/bjoc.9.128

• chiral Lewis acid and these substrates. Keywords: cascade; cyclization; enantioselective; free radical; Lewis acid; radical; Introduction Strategies involving a cascade process offer the advantage of multiple carbon–carbon and/or carbon–heteroatom bond formations in a single operation. Radical

Mechanochemistry assisted asymmetric organocatalysis: A sustainable approach

• Pankaj Chauhan and
• Swapandeep Singh Chimni

Beilstein J. Org. Chem. 2012, 8, 2132–2141, doi:10.3762/bjoc.8.240

• , which helps in the easy isolation of products. Besides the significant progress in the application of mechanochemical techniques in asymmetric organocatalysis, there exists a lot of scope for other asymmetric reactions ranging from simple carbon–carbon, and carbon–heteroatom bond formation to more

N-Heterocyclic carbene–palladium(II)-1-methylimidazole complex catalyzed Mizoroki–Heck reaction of aryl chlorides with styrenes

• Ting-Ting Gao,
• Ai-Ping Jin and
• Li-Xiong Shao

Beilstein J. Org. Chem. 2012, 8, 1916–1919, doi:10.3762/bjoc.8.222

• phosphine ligands, which can then increase the catalytic activity of the metal centre and the stability of the NHC–metal complexes, have attracted growing attention in the metal-catalyzed carbon–carbon and carbon–heteroatom bond-formation reactions during the past two decades [10][11][12][13][14][15

Hypervalent iodine(III)-induced methylene acetoxylation of 3-oxo-N-substituted butanamides

• Wei-Bing Liu,
• Cui Chen,
• Qing Zhang and
• Zhi-Bo Zhu

Beilstein J. Org. Chem. 2011, 7, 1436–1440, doi:10.3762/bjoc.7.167

• : 1-carbamoyl-2-oxopropyl acetate derivatives; C-hetero bond; (diacetoxyiodo)benzene; methylene acetoxylation; Introduction Carbon–carbon, carbon–heteroatom bond formation leading to useful molecular structures is one of the most interesting and challenging research topics in organic chemistry [1][2

When gold can do what iodine cannot do: A critical comparison

• Sara Hummel and
• Stefan F. Kirsch

Beilstein J. Org. Chem. 2011, 7, 847–859, doi:10.3762/bjoc.7.97

• majority of gold-catalyzed cyclization modes have involved initial carbon-heteroatom bond formation [7][10]. As a general rule, the nucleophilic attack of a carbonyl (or imine) group onto an alkyne activated by gold-complexation generates first an oxonium (iminium) ion species, the cationic character of

• being solely anti. This reaction is an excellent example that underlines the great potential of the alkynophilicity of the gold metal center. While gold-catalysts make both carbon–carbon and carbon–heteroatom bond formation possible, the analogous process with iodine electrophiles was not realized

Unusual behavior in the reactivity of 5-substituted-1H-tetrazoles in a resistively heated microreactor

• Bernhard Gutmann,
• Toma N. Glasnov,
• Tahseen Razzaq,
• Walter Goessler,
• Dominique M. Roberge and
• C. Oliver Kappe

Beilstein J. Org. Chem. 2011, 7, 503–517, doi:10.3762/bjoc.7.59

• Figure S5 in Supporting Information File 1) clearly reveals that the age/history of the reactor can have an influence on the chemical transformations occurring inside these flow devices. The use of transition metal catalysts for carbon–carbon or carbon–heteroatom bond formation under continuous flow

Reduction of arenediazonium salts by tetrakis(dimethylamino)ethylene (TDAE): Efficient formation of products derived from aryl radicals

• Mohan Mahesh,
• John A. Murphy,
• Franck LeStrat and
• Hans Peter Wessel

Beilstein J. Org. Chem. 2009, 5, No. 1, doi:10.3762/bjoc.5.1

• : cyclization; electron transfer; indole; indoline; radical; Introduction Arenediazonium salts have long proved useful as sources of aryl radicals in many reactions featuring carbon-carbon (e.g., Meerwein [1], Pschorr [2][3], Gomberg [3] reactions) and carbon-heteroatom bond (e.g., Sandmeyer [4]) formation