Separation and identification of indene–C70 bisadduct isomers
- Bolong Zhang,
- Jegadesan Subbiah,
- David J. Jones and
- Wallace W. H. Wong
Beilstein J. Org. Chem. 2016, 12, 903–911, doi:10.3762/bjoc.12.88
A robust synthesis of 7,8-didemethyl-8-hydroxy-5-deazariboflavin
- Matthias Bender,
- Henrik Mouritsen and
- Jens Christoffers
Beilstein J. Org. Chem. 2016, 12, 912–917, doi:10.3762/bjoc.12.89
1H-Imidazol-4(5H)-ones and thiazol-4(5H)-ones as emerging pronucleophiles in asymmetric catalysis
- Antonia Mielgo and
- Claudio Palomo
Beilstein J. Org. Chem. 2016, 12, 918–936, doi:10.3762/bjoc.12.90
Superstructures with cyclodextrins: chemistry and applications III
- Gerhard Wenz and
- Eric Monflier
Beilstein J. Org. Chem. 2016, 12, 937–938, doi:10.3762/bjoc.12.91
Stimuli-responsive HBPS-g-PDMAEMA and its application as nanocarrier in loading hydrophobic molecules
- Yongsheng Chen,
- Li Wang,
- Haojie Yu,
- Zain-Ul-Abdin,
- Ruoli Sun,
- Guanghui Jing,
- Rongbai Tong and
- Zheng Deng
Beilstein J. Org. Chem. 2016, 12, 939–949, doi:10.3762/bjoc.12.92
Reactions of N,3-diarylpropiolamides with arenes under superelectrophilic activation: synthesis of 4,4-diaryl-3,4-dihydroquinolin-2(1H)-ones and their derivatives
- Larisa Yu. Gurskaya,
- Diana S. Belyanskaya,
- Dmitry S. Ryabukhin,
- Denis I. Nilov,
- Irina A. Boyarskaya and
- Aleksander V. Vasilyev
Beilstein J. Org. Chem. 2016, 12, 950–956, doi:10.3762/bjoc.12.93
One-pot synthesis of enantiomerically pure N-protected allylic amines from N-protected α-amino esters
- Gastón Silveira-Dorta,
- Sergio J. Álvarez-Méndez,
- Víctor S. Martín and
- José M. Padrón
Beilstein J. Org. Chem. 2016, 12, 957–962, doi:10.3762/bjoc.12.94
A cross-metathesis approach to novel pantothenamide derivatives
- Jinming Guan,
- Matthew Hachey,
- Lekha Puri,
- Vanessa Howieson,
- Kevin J. Saliba and
- Karine Auclair
Beilstein J. Org. Chem. 2016, 12, 963–968, doi:10.3762/bjoc.12.95
Marine-derived myxobacteria of the suborder Nannocystineae: An underexplored source of structurally intriguing and biologically active metabolites
- Antonio Dávila-Céspedes,
- Peter Hufendiek,
- Max Crüsemann,
- Till F. Schäberle and
- Gabriele M. König
Beilstein J. Org. Chem. 2016, 12, 969–984, doi:10.3762/bjoc.12.96
The synthesis of functionalized bridged polycycles via C–H bond insertion
- Jiun-Le Shih,
- Po-An Chen and
- Jeremy A. May
Beilstein J. Org. Chem. 2016, 12, 985–999, doi:10.3762/bjoc.12.97
Catalytic asymmetric synthesis of biologically important 3-hydroxyoxindoles: an update
- Bin Yu,
- Hui Xing,
- De-Quan Yu and
- Hong-Min Liu
Beilstein J. Org. Chem. 2016, 12, 1000–1039, doi:10.3762/bjoc.12.98
Cationic Pd(II)-catalyzed C–H activation/cross-coupling reactions at room temperature: synthetic and mechanistic studies
- Takashi Nishikata,
- Alexander R. Abela,
- Shenlin Huang and
- Bruce H. Lipshutz
Beilstein J. Org. Chem. 2016, 12, 1040–1064, doi:10.3762/bjoc.12.99
Antibacterial structure–activity relationship studies of several tricyclic sulfur-containing flavonoids
- Lucian G. Bahrin,
- Henning Hopf,
- Peter G. Jones,
- Laura G. Sarbu,
- Cornelia Babii,
- Alina C. Mihai,
- Marius Stefan and
- Lucian M. Birsa
Beilstein J. Org. Chem. 2016, 12, 1065–1071, doi:10.3762/bjoc.12.100
Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides
- Long-Yi Xi,
- Ruo-Yi Zhang,
- Lei Shi,
- Shan-Yong Chen and
- Xiao-Qi Yu
Beilstein J. Org. Chem. 2016, 12, 1072–1078, doi:10.3762/bjoc.12.101
Bifunctional catalysis
- Darren J. Dixon
Beilstein J. Org. Chem. 2016, 12, 1079–1080, doi:10.3762/bjoc.12.102
Efficient syntheses of climate relevant isoprene nitrates and (1R,5S)-(−)-myrtenol nitrate
- Sean P. Bew,
- Glyn D. Hiatt-Gipson,
- Graham P. Mills and
- Claire E. Reeves
Beilstein J. Org. Chem. 2016, 12, 1081–1095, doi:10.3762/bjoc.12.103
Towards the total synthesis of keramaphidin B
- Pavol Jakubec,
- Alistair J. M. Farley and
- Darren J. Dixon
Beilstein J. Org. Chem. 2016, 12, 1096–1100, doi:10.3762/bjoc.12.104
Supramolecular chemistry at the interface of biology, materials and medicine
- Eric V. Anslyn and
- Steven C. Zimmerman
Beilstein J. Org. Chem. 2016, 12, 1101–1102, doi:10.3762/bjoc.12.105
The role of alkyl substituents in deazaadenine-based diarylethene photoswitches
- Christopher Sarter,
- Michael Heimes and
- Andres Jäschke
Beilstein J. Org. Chem. 2016, 12, 1103–1110, doi:10.3762/bjoc.12.106
Modular synthesis of the pyrimidine core of the manzacidins by divergent Tsuji–Trost coupling
- Sebastian Bretzke,
- Stephan Scheeff,
- Felicitas Vollmeyer,
- Friederike Eberhagen,
- Frank Rominger and
- Dirk Menche
Beilstein J. Org. Chem. 2016, 12, 1111–1121, doi:10.3762/bjoc.12.107
Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylation
- Yunyun Liu,
- Yi Zhang,
- Xiaoji Cao and
- Jie-Ping Wan
Beilstein J. Org. Chem. 2016, 12, 1122–1126, doi:10.3762/bjoc.12.108
Synthesis of a deuterated probe for the confocal Raman microscopy imaging of squalenoyl nanomedicines
- Eric Buchy,
- Branko Vukosavljevic,
- Maike Windbergs,
- Dunja Sobot,
- Camille Dejean,
- Simona Mura,
- Patrick Couvreur and
- Didier Desmaële
Beilstein J. Org. Chem. 2016, 12, 1127–1135, doi:10.3762/bjoc.12.109
Chiral cyclopentadienylruthenium sulfoxide catalysts for asymmetric redox bicycloisomerization
- Barry M. Trost,
- Michael C. Ryan and
- Meera Rao
Beilstein J. Org. Chem. 2016, 12, 1136–1152, doi:10.3762/bjoc.12.110
Synthesis of 2-oxindoles via 'transition-metal-free' intramolecular dehydrogenative coupling (IDC) of sp2 C–H and sp3 C–H bonds
- Nivesh Kumar,
- Santanu Ghosh,
- Subhajit Bhunia and
- Alakesh Bisai
Beilstein J. Org. Chem. 2016, 12, 1153–1169, doi:10.3762/bjoc.12.111
Synthesis of highly functionalized 2,2'-bipyridines by cyclocondensation of β-ketoenamides – scope and limitations
- Paul Hommes and
- Hans-Ulrich Reissig
Beilstein J. Org. Chem. 2016, 12, 1170–1177, doi:10.3762/bjoc.12.112
Unusual traits of cis and trans-2,3-dibromo-1,1-dimethylindane on the way from 1,1-dimethylindene to 2-bromo-, 3-bromo-, and 2,3-dibromo-1,1-dimethylindene
- Rudolf Knorr,
- David S. Stephenson,
- Ernst Lattke,
- Petra Böhrer and
- Jakob Ruhdorfer
Beilstein J. Org. Chem. 2016, 12, 1178–1184, doi:10.3762/bjoc.12.113
NeoPHOX – a structurally tunable ligand system for asymmetric catalysis
- Jaroslav Padevět,
- Marcus G. Schrems,
- Robin Scheil and
- Andreas Pfaltz
Beilstein J. Org. Chem. 2016, 12, 1185–1195, doi:10.3762/bjoc.12.114
Biradical vs singlet oxygen photogeneration in suprofen–cholesterol systems
- Fabrizio Palumbo,
- Francisco Bosca,
- Isabel M. Morera,
- Inmaculada Andreu and
- Miguel A. Miranda
Beilstein J. Org. Chem. 2016, 12, 1196–1202, doi:10.3762/bjoc.12.115
