Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives

• Imane Nekkaa,
• Márta Palkó,
• István M. Mándity and
• Ferenc Fülöp

Beilstein J. Org. Chem. 2018, 14, 318–324, doi:10.3762/bjoc.14.20

• addition, they are present in several natural frameworks [42][43][44]. We wanted to exploit the benefits of flow processing for reaction optimization and synthesis and develop novel sustainable synthetic methodologies with possible useful applications for the pharmaceutical industry. Our results show that

Aminosugar-based immunomodulator lipid A: synthetic approaches

• Alla Zamyatina

Beilstein J. Org. Chem. 2018, 14, 25–53, doi:10.3762/bjoc.14.3

• availability of homogeneous structurally distinct lipid A, the development of divergent and reproducible approaches for the synthesis of various types of lipid A has become a subject of considerable importance. This review focuses on recent advances in synthetic methodologies toward LPS substructures

Mechanochemical synthesis of small organic molecules

• Tapas Kumar Achar,
• Anima Bose and
• Prasenjit Mal

Beilstein J. Org. Chem. 2017, 13, 1907–1931, doi:10.3762/bjoc.13.186

• . Improvement in new synthetic methodologies under mechanomilling conditions with better results are always demanding, rather than “greening” the solution phase synthesis. Mechanochemical aldol condensation reactions [48]. Enantioselective organocatalyzed aldol reactions under mechanomilling. a) Based on binam

An effective Pd nanocatalyst in aqueous media: stilbene synthesis by Mizoroki–Heck coupling reaction under microwave irradiation

• Carolina S. García,
• Paula M. Uberman and
• Sandra E. Martín

Beilstein J. Org. Chem. 2017, 13, 1717–1727, doi:10.3762/bjoc.13.166

• an economic and environmental standpoint, it is highly desirable to develop more environmentally friendly synthetic methodologies. Several studies were dedicated to the design of a novel catalytic system, that are more accessible, robust, efficient and ligand-free [19]. In that sense, nanoparticles

Nucleophilic and electrophilic cyclization of N-alkyne-substituted pyrrole derivatives: Synthesis of pyrrolopyrazinone, pyrrolotriazinone, and pyrrolooxazinone moieties

• Işıl Yenice,
• Sinan Basceken and
• Metin Balci

Beilstein J. Org. Chem. 2017, 13, 825–834, doi:10.3762/bjoc.13.83

• synthetic method for the construction of the pyrrolopyrazinone core structure as well as for its derivatives is not described in the literature [14]. Recently, we developed new synthetic methodologies for the synthesis of various pyrrole-fused new heterocycles using alkyne cyclization reactions [15][16][17

Fluorescent carbon dots from mono- and polysaccharides: synthesis, properties and applications

• Stephen Hill and
• M. Carmen Galan

Beilstein J. Org. Chem. 2017, 13, 675–693, doi:10.3762/bjoc.13.67

• wide range of in vivo applications, which has been the topic of several recent reviews [13][14][15]. Following the serendipitous discovery by Xu et al. during the separation and purification of single-walled carbon nanotubes (SWCNTs) [16], the development of synthetic methodologies to access these

Chiral ammonium betaine-catalyzed asymmetric Mannich-type reaction of oxindoles

• Masahiro Torii,
• Kohsuke Kato,
• Daisuke Uraguchi and
• Takashi Ooi

Beilstein J. Org. Chem. 2016, 12, 2099–2103, doi:10.3762/bjoc.12.199

• important class of biologically relevant molecules, and numerous efforts have been made for the development of reliable synthetic methodologies to enable the installation of the C-3 stereogenic center [1][2][3][4]. Among them, the direct stereoselective functionalization of 3-monosubstituted oxindoles is a

Versatile deprotonated NHC: C,N-bridged dinuclear iridium and rhodium complexes

• Albert Poater

Beilstein J. Org. Chem. 2016, 12, 117–124, doi:10.3762/bjoc.12.13

• ], substrate recognition [29] and/or biological systems [30][31]. Among the synthetic methodologies to access to pNHC metal complexes [32][33][34][35][36][37][38][39][40], recently N-arylimine functionalized pNHC iridium complexes were obtained using excess of [Ir(cod)(µ-Cl)]2 [41], and next deprotonation of

An efficient synthesis of N-substituted 3-nitrothiophen-2-amines

• Sundaravel Vivek Kumar,
• Shanmugam Muthusubramanian,
• J. Carlos Menéndez and
• Subbu Perumal

Beilstein J. Org. Chem. 2015, 11, 1707–1712, doi:10.3762/bjoc.11.185

• limitations in existing synthetic methodologies, particularly in the direct preparation of N-substituted amino derivatives. 2-Aminothiophenes have traditionally been synthesized from mercapto- or halogen-substituted thiophenes through nucleophilic displacements [19]. More recently, these derivatives have been

Synthesis of 1,2-cis-2-C-branched aryl-C-glucosides via desulfurization of carbohydrate based hemithioacetals

• Henok H. Kinfe,
• Fanuel M. Mebrahtu,
• Mandlenkosi M. Manana,
• Kagiso Madumo and
• Mokela S. Sokamisa

Beilstein J. Org. Chem. 2015, 11, 583–588, doi:10.3762/bjoc.11.64

• the regioselective ring opening of 1,2-cyclopropanated carbohydrates and the radical addition reaction of glycals [11][12][13][14][15]. Although the synthetic methodologies developed for the synthesis of C-glycosides and 2-C-branched sugars are extensively studied, the synthesis of 1,2-cis-2-C

Electrocarboxylation: towards sustainable and efficient synthesis of valuable carboxylic acids

• Roman Matthessen,
• Jan Fransaer,
• Koen Binnemans and
• Dirk E. De Vos

Beilstein J. Org. Chem. 2014, 10, 2484–2500, doi:10.3762/bjoc.10.260

• possibilities and challenges of implementing other synthetic methodologies. In view of potential industrial application, the choice of reactor setup, electrode type and reaction pathway has a large influence on the sustainability and efficiency of the process. Keywords: carbon dioxide; carboxylic acids

Expedient synthesis of 1,6-anhydro-α-D-galactofuranose, a useful intermediate for glycobiological tools

• Luciana Baldoni and
• Carla Marino

Beilstein J. Org. Chem. 2014, 10, 1651–1656, doi:10.3762/bjoc.10.172

• complex products and bioactive compounds. Among the glycosans, the anhydro sugars involving the anomeric center in the ring formation, the 1,6-anhydro sugars are the most common and useful building blocks [1][2]. They can play a role in synthetic methodologies aiming at the obtainment of regioselectively

Synthesis of chiral N-phosphoryl aziridines through enantioselective aziridination of alkenes with phosphoryl azide via Co(II)-based metalloradical catalysis

• Jingran Tao,
• Li-Mei Jin and
• X. Peter Zhang

Beilstein J. Org. Chem. 2014, 10, 1282–1289, doi:10.3762/bjoc.10.129

• efforts have been made for the construction of this class of nitrogen-containing three-membered ring compounds [3][4][5][6][7][8]. Among synthetic methodologies, catalytic aziridination of alkenes with nitrene sources via “C2 + N1” addition has received the most attention because of the abundance of both

Clean and fast cross-coupling of aryl halides in one-pot

• Valerica Pandarus,
• Geneviève Gingras,
• François Béland,
• Rosaria Ciriminna and
• Mario Pagliaro

Beilstein J. Org. Chem. 2014, 10, 897–901, doi:10.3762/bjoc.10.87

• . As the fine chemicals and pharmaceutical industries are eventually adopting green chemistry synthetic methodologies [13], this method provides both industries with a clean route to valued compounds that are widely used in many industrial sectors. Chemical structure of SiliaCat DPP-Pd. Heterogeneously

Aza-Diels–Alder reaction between N-aryl-1-oxo-1H-isoindolium ions and tert-enamides: Steric effects on reaction outcome

• Amitabh Jha,
• Ting-Yi Chou,
• Zainab ALJaroudi,
• Bobby D. Ellis and
• T. Stanley Cameron

Beilstein J. Org. Chem. 2014, 10, 848–857, doi:10.3762/bjoc.10.81

• been studied. In continuation of our efforts on the development of novel synthetic methodologies [27][28][29][30][31][32][33][34][35][36], we report herein a systematic study of steric and electronic effects of aryl substituents leading to substituted 6,6a-dihydroisoindolo[2,1-a]quinolin-11(5H)-ones

An oxidative amidation and heterocyclization approach for the synthesis of β-carbolines and dihydroeudistomin Y

• Suresh Babu Meruva,
• Akula Raghunadh,
• Raghavendra Rao Kamaraju,
• U. K. Syam Kumar and
• P. K. Dubey

Beilstein J. Org. Chem. 2014, 10, 471–480, doi:10.3762/bjoc.10.45

• -carbolines or dihydroeudistomin. The previously developed synthetic methodologies in our laboratory [19][20][21][22][23][24] were utilized for the synthesis of eudistomin Y (6) and its analogues The disconnection approach employed in the synthesis of 1-benzoyl-β-carboline is described in Scheme 1

Synthesis and stereochemical assignments of diastereomeric Ni(II) complexes of glycine Schiff base with (R)-2-(N-{2-[N-alkyl-N-(1-phenylethyl)amino]acetyl}amino)benzophenone; a case of configurationally stable stereogenic nitrogen

• Hiroki Moriwaki,
• Daniel Resch,
• Hengguang Li,
• Iwao Ojima,
• Ryosuke Takeda,
• José Luis Aceña and
• Vadim A. Soloshonok

Beilstein J. Org. Chem. 2014, 10, 442–448, doi:10.3762/bjoc.10.41

• currently available methodologies [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30]; however, the chemistry of α-AAs continues to evolve [31][32][33][34][35][36][37][38]. Many of the reported synthetic methodologies have shown preference for

Diversity-oriented synthesis of dihydrobenzoxazepinones by coupling the Ugi multicomponent reaction with a Mitsunobu cyclization

• Lisa Moni,
• Luca Banfi,
• Andrea Basso,
• Alice Brambilla and
• Renata Riva

Beilstein J. Org. Chem. 2014, 10, 209–212, doi:10.3762/bjoc.10.16

• Lorenzo Giardini and Sara Piano for preliminary exploratory experiments, Andrea Armirotti and Martina Spallarossa for HRMS, PRIN 2009 ("Synthetic Methodologies for Generation of Biologically Relevant Molecular Diversity") and the University of Genova for funding.

New developments in gold-catalyzed manipulation of inactivated alkenes

• Michel Chiarucci and
• Marco Bandini

Beilstein J. Org. Chem. 2013, 9, 2586–2614, doi:10.3762/bjoc.9.294

• . Cooperative [Au(I)]/menthol catalysis for the enantioselective intramolecular hydroamination of dienes. Acknowledgements Acknowledgment is made to Progetto FIRB “Futuro in Ricerca” Innovative sustainable synthetic methodologies for C–H activation processes, (MIUR, Rome) and the Università di Bologna.

An overview of the synthetic routes to the best selling drugs containing 6-membered heterocycles

• Marcus Baumann and
• Ian R. Baxendale

Beilstein J. Org. Chem. 2013, 9, 2265–2319, doi:10.3762/bjoc.9.265

• outlay [5]. As a result pharmaceutical companies are constantly seeking ways to accelerate this development process by adopting new synthetic methodologies and enabling technologies in order to profitably generate new medications for both old and new targets [6]. By reviewing the synthetic routes used to

Straightforward synthesis of a tetrasaccharide repeating unit corresponding to the O-antigen of Escherichia coli O16

• Manas Jana and
• Anup Kumar Misra

Beilstein J. Org. Chem. 2013, 9, 1757–1762, doi:10.3762/bjoc.9.203

• summary, a straightforward synthetic strategy was developed for the synthesis of the tetrasaccharide 1 as its p-methoxyphenyl glycoside corresponding to the O-antigen of E. coli O16. The target compound was synthesized by using a minimum number of steps and by applying recently developed elegant synthetic

• methodologies. Both the yields of the protecting group manipulations and the stereoselectivity of the glycosylation reactions were excellent. Experimental General methods are similar as described in an earlier report [21]. p-Methoxyphenyl (2-O-acetyl-4-O-benzyl-α-L-rhamnopyranosyl)-(1→3)-2-azido-4,6-O

Organocatalyzed enantioselective desymmetrization of aziridines and epoxides

• Ping-An Wang

Beilstein J. Org. Chem. 2013, 9, 1677–1695, doi:10.3762/bjoc.9.192

• desymmetrization of meso-aziridines and meso-epoxides. Undoubtedly, these synthetic methodologies will continue to demonstrate their versatile utilities in organic synthesis. However, there are some difficulties that should be pointed out. Organocatalysts for the enantioselective desymmetrization of meso

Coupling of C-nitro-NH-azoles with arylboronic acids. A route to N-aryl-C-nitroazoles

• Marta K. Kurpet,
• Aleksandra Dąbrowska,
• Małgorzata M. Jarosz,
• Katarzyna Kajewska-Kania,
• Nikodem Kuźnik and
• Jerzy W. Suwiński

Beilstein J. Org. Chem. 2013, 9, 1517–1525, doi:10.3762/bjoc.9.173

• containing a base, both of which are necessary for providing good yields of the products. The method represents an important supplement to the synthetic methodologies for the preparation of N-aryl-C-nitroazoles and can be successfully applied to the synthesis of a series of diverse C-nitroazoles

Amyloid-β probes: Review of structure–activity and brain-kinetics relationships

• Todd J. Eckroat,
• Abdelrahman S. Mayhoub and
• Sylvie Garneau-Tsodikova

Beilstein J. Org. Chem. 2013, 9, 1012–1044, doi:10.3762/bjoc.9.116

• efforts to develop chemical probes to detect pathophysiological hallmarks of AD, such as amyloid-β plaques, for diagnosis and monitoring of therapeutic efficacy. This review provides a survey of chemical probes developed to date for AD with emphasis on synthetic methodologies and structure–activity

Alternaric acid: formal synthesis and related studies

• Michael C. Slade and
• Jeffrey S. Johnson

Beilstein J. Org. Chem. 2013, 9, 166–172, doi:10.3762/bjoc.9.19

• endeavors, both in natural-product synthesis and synthetic methodologies [20]. Key to their use in a variety of contexts is the ability of silyl glyoxylates to function as linchpin synthons for geminal coupling of nucleophile/electrophile pairs at a glycolic acid subunit (Scheme 1A), which allows the rapid