Photoredox-catalyzed silyldifluoromethylation of silyl enol ethers
- Vyacheslav I. Supranovich,
- Vitalij V. Levin and
- Alexander D. Dilman
Beilstein J. Org. Chem. 2020, 16, 1550–1553, doi:10.3762/bjoc.16.126
Mechanochemical green synthesis of hyper-crosslinked cyclodextrin polymers
- Alberto Rubin Pedrazzo,
- Fabrizio Caldera,
- Marco Zanetti,
- Silvia Lucia Appleton,
- Nilesh Kumar Dhakar and
- Francesco Trotta
Beilstein J. Org. Chem. 2020, 16, 1554–1563, doi:10.3762/bjoc.16.127
Five-component, one-pot synthesis of an electroactive rotaxane comprising a bisferrocene macrocycle
- Natalie Lagesse,
- Luca Pisciottani,
- Maxime Douarre,
- Pascale Godard,
- Brice Kauffmann,
- Vicente Martí-Centelles and
- Nathan D. McClenaghan
Beilstein J. Org. Chem. 2020, 16, 1564–1571, doi:10.3762/bjoc.16.128
NHC-catalyzed enantioselective synthesis of β-trifluoromethyl-β-hydroxyamides
- Alyn T. Davies,
- Mark D. Greenhalgh,
- Alexandra M. Z. Slawin and
- Andrew D. Smith
Beilstein J. Org. Chem. 2020, 16, 1572–1578, doi:10.3762/bjoc.16.129
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
A dynamic combinatorial library for biomimetic recognition of dipeptides in water
- Florian Klepel and
- Bart Jan Ravoo
Beilstein J. Org. Chem. 2020, 16, 1588–1595, doi:10.3762/bjoc.16.131
Antibacterial scalarane from Doriprismatica stellata nudibranchs (Gastropoda, Nudibranchia), egg ribbons, and their dietary sponge Spongia cf. agaricina (Demospongiae, Dictyoceratida)
- Cora Hertzer,
- Stefan Kehraus,
- Nils Böhringer,
- Fontje Kaligis,
- Robert Bara,
- Dirk Erpenbeck,
- Gert Wörheide,
- Till F. Schäberle,
- Heike Wägele and
- Gabriele M. König
Beilstein J. Org. Chem. 2020, 16, 1596–1605, doi:10.3762/bjoc.16.132
Synthesis of new dihydroberberine and tetrahydroberberine analogues and evaluation of their antiproliferative activity on NCI-H1975 cells
- Giacomo Mari,
- Lucia De Crescentini,
- Serena Benedetti,
- Francesco Palma,
- Stefania Santeusanio and
- Fabio Mantellini
Beilstein J. Org. Chem. 2020, 16, 1606–1616, doi:10.3762/bjoc.16.133
Facile synthesis of 7-alkyl-1,2,3,4-tetrahydro-1,8-naphthyridines as arginine mimetics using a Horner–Wadsworth–Emmons-based approach
- Rhys A. Lippa,
- John A. Murphy and
- Tim N. Barrett
Beilstein J. Org. Chem. 2020, 16, 1617–1626, doi:10.3762/bjoc.16.134
Fluorohydration of alkynes via I(I)/I(III) catalysis
- Jessica Neufeld,
- Constantin G. Daniliuc and
- Ryan Gilmour
Beilstein J. Org. Chem. 2020, 16, 1627–1635, doi:10.3762/bjoc.16.135
Rearrangement of o-(pivaloylaminomethyl)benzaldehydes: an experimental and computational study
- Csilla Hargitai,
- Györgyi Koványi-Lax,
- Tamás Nagy,
- Péter Ábrányi-Balogh,
- András Dancsó,
- Gábor Tóth,
- Judit Halász,
- Angéla Pandur,
- Gyula Simig and
- Balázs Volk
Beilstein J. Org. Chem. 2020, 16, 1636–1648, doi:10.3762/bjoc.16.136
Models of necessity
- Timothy Clark and
- Martin G. Hicks
Beilstein J. Org. Chem. 2020, 16, 1649–1661, doi:10.3762/bjoc.16.137
Pauson–Khand reaction of fluorinated compounds
- Jorge Escorihuela,
- Daniel M. Sedgwick,
- Alberto Llobat,
- Mercedes Medio-Simón,
- Pablo Barrio and
- Santos Fustero
Beilstein J. Org. Chem. 2020, 16, 1662–1682, doi:10.3762/bjoc.16.138
Clickable azide-functionalized bromoarylaldehydes – synthesis and photophysical characterization
- Dominik Göbel,
- Marius Friedrich,
- Enno Lork and
- Boris J. Nachtsheim
Beilstein J. Org. Chem. 2020, 16, 1683–1692, doi:10.3762/bjoc.16.139
Synthesis of Streptococcus pneumoniae serotype 9V oligosaccharide antigens
- Sharavathi G. Parameswarappa,
- Claney L. Pereira and
- Peter H. Seeberger
Beilstein J. Org. Chem. 2020, 16, 1693–1699, doi:10.3762/bjoc.16.140
Synthesis of the tetrasaccharide repeating unit of the O-specific polysaccharide of Azospirillum doebereinerae type strain GSF71T using linear and one-pot iterative glycosylations
- Arin Gucchait,
- Pradip Shit and
- Anup Kumar Misra
Beilstein J. Org. Chem. 2020, 16, 1700–1705, doi:10.3762/bjoc.16.141
Microwave-assisted efficient one-pot synthesis of N2-(tetrazol-5-yl)-6-aryl/heteroaryl-5,6-dihydro-1,3,5-triazine-2,4-diamines
- Moustafa Sherief Moustafa,
- Ramadan Ahmed Mekheimer,
- Saleh Mohammed Al-Mousawi,
- Mohamed Abd-Elmonem,
- Hesham El-Zorba,
- Afaf Mohamed Abdel Hameed,
- Tahany Mahmoud Mohamed and
- Kamal Usef Sadek
Beilstein J. Org. Chem. 2020, 16, 1706–1712, doi:10.3762/bjoc.16.142
One-pot synthesis of isosorbide from cellulose or lignocellulosic biomass: a challenge?
- Isaline Bonnin,
- Raphaël Mereau,
- Thierry Tassaing and
- Karine De Oliveira Vigier
Beilstein J. Org. Chem. 2020, 16, 1713–1721, doi:10.3762/bjoc.16.143
Tuneable access to indole, indolone, and cinnoline derivatives from a common 1,4-diketone Michael acceptor
- Dalel El-Marrouki,
- Sabrina Touchet,
- Abderrahmen Abdelli,
- Hédi M’Rabet,
- Mohamed Lotfi Efrit and
- Philippe C. Gros
Beilstein J. Org. Chem. 2020, 16, 1722–1731, doi:10.3762/bjoc.16.144
Nonenzymatic synthesis of anomerically pure, mannosyl-based molecular probes for scramblase identification studies
- Giovanni Picca,
- Markus Probst,
- Simon M. Langenegger,
- Oleg Khorev,
- Peter Bütikofer,
- Anant K. Menon and
- Robert Häner
Beilstein J. Org. Chem. 2020, 16, 1732–1739, doi:10.3762/bjoc.16.145
Et3N/DMSO-supported one-pot synthesis of highly fluorescent β-carboline-linked benzothiophenones via sulfur insertion and estimation of the photophysical properties
- Dharmender Singh,
- Vipin Kumar and
- Virender Singh
Beilstein J. Org. Chem. 2020, 16, 1740–1753, doi:10.3762/bjoc.16.146
When metal-catalyzed C–H functionalization meets visible-light photocatalysis
- Lucas Guillemard and
- Joanna Wencel-Delord
Beilstein J. Org. Chem. 2020, 16, 1754–1804, doi:10.3762/bjoc.16.147
