Published in Org Biomol Chem on March 02, 2016
Nonracemic Betti base as a new chiral auxiliary: application to total syntheses of enantiopure (2S,6R)-dihydropinidine and (2S,6R)-isosolenopsins. J Org Chem (2005) 2.19
Solar water oxidation by composite catalyst/alpha-Fe(2)O(3) photoanodes. J Am Chem Soc (2009) 1.35
25th anniversary article: semiconductor nanowires--synthesis, characterization, and applications. Adv Mater (2014) 1.33
Retromer is required for apoptotic cell clearance by phagocytic receptor recycling. Science (2010) 1.30
Hypoxia-inducible factor-1 promotes pancreatic ductal adenocarcinoma invasion and metastasis by activating transcription of the actin-bundling protein fascin. Cancer Res (2014) 1.25
Solution-liquid-solid growth of semiconductor nanowires. Inorg Chem (2006) 1.18
Phosphine-catalyzed asymmetric additions of malonate esters to {gamma}-substituted allenoates and allenamides. Proc Natl Acad Sci U S A (2010) 1.17
Nickel-catalyzed enantioselective cross-couplings of racemic secondary electrophiles that bear an oxygen leaving group. J Am Chem Soc (2012) 1.08
Workhorse semilocal density functional for condensed matter physics and quantum chemistry. Phys Rev Lett (2009) 1.00
Caenorhabditis elegans protein arginine methyltransferase PRMT-5 negatively regulates DNA damage-induced apoptosis. PLoS Genet (2009) 1.00
Enantioselective Carbon-Sulfur Bond Formation: γ Additions of Aryl Thiols to Allenoates Catalyzed by a Chiral Phosphepine. Chem Sci (2011) 0.93
Ligand-controlled remarkable regio- and stereodivergence in intermolecular hydrosilylation of internal alkynes: experimental and theoretical studies. J Am Chem Soc (2013) 0.91
Zn-doped p-type gallium phosphide nanowire photocathodes from a surfactant-free solution synthesis. Nano Lett (2012) 0.90
Phase-selective cation-exchange chemistry in sulfide nanowire systems. J Am Chem Soc (2014) 0.88
Catalytic enantioselective synthesis of tetrahydroisoquinolines and their analogues bearing a C4 stereocenter: formal synthesis of (+)-(8S,13R)-cyclocelabenzine. Chemistry (2013) 0.83
Dithiafulvenyl unit as a new donor for high-efficiency dye-sensitized solar cells: synthesis and demonstration of a family of metal-free organic sensitizers. Org Lett (2012) 0.82
Chiral phosphoric acid catalyzed enantioselective desymmetrization of meso-epoxides by thiols. Org Lett (2013) 0.82
Catalytic asymmetric nucleophilic openings of 3-substituted oxetanes. Org Biomol Chem (2014) 0.82
Organocatalytic asymmetric synthesis of 1,1-diarylethanes by transfer hydrogenation. J Am Chem Soc (2014) 0.82
Catalytic enantioselective intermolecular desymmetrization of 3-substituted oxetanes. Angew Chem Int Ed Engl (2013) 0.81
A new strategy for efficient synthesis of medium and large ring lactones without high dilution or slow addition. J Am Chem Soc (2013) 0.80
Iridium-catalyzed intermolecular azide-alkyne cycloaddition of internal thioalkynes under mild conditions. Angew Chem Int Ed Engl (2014) 0.80
Enantioselective synthesis of β,γ-unsaturated α-fluoroesters catalyzed by N-heterocyclic carbenes. Angew Chem Int Ed Engl (2012) 0.79
Synthesis of eight-membered lactones: intermolecular [6+2] cyclization of amphoteric molecules with siloxy alkynes. Angew Chem Int Ed Engl (2012) 0.79
Wogonin protects rat dorsal root ganglion neurons against tunicamycin-induced ER stress through the PERK-eIF2α-ATF4 signaling pathway. J Mol Neurosci (2014) 0.79
Complex bioactive alkaloid-type polycycles through efficient catalytic asymmetric multicomponent aza-Diels-Alder reaction of indoles with oxetane as directing group. Angew Chem Int Ed Engl (2013) 0.79
Organocatalytic enantioselective synthesis of 2,3-allenoates by intermolecular addition of nitroalkanes to activated enynes. J Am Chem Soc (2013) 0.79
Enantio- and diastereoselective assembly of tetrahydrofuran and tetrahydropyran skeletons with all-carbon-substituted quaternary stereocenters. Angew Chem Int Ed Engl (2013) 0.78
Organocatalytic enantio- and diastereoselective synthesis of 1,2-dihydronaphthalenes from isobenzopyrylium ions. J Am Chem Soc (2015) 0.78
Stereoselective synthesis of aminoindanols via an efficient cascade aza-Michael-aldol reaction. Chem Commun (Camb) (2012) 0.78
Highly Regio- and Stereoselective Hydrosilylation of Internal Thioalkynes under Mild Conditions. Angew Chem Int Ed Engl (2015) 0.77
Catalytic asymmetric α-aldol reaction of vinylogous N-heterocyclic carbene enolates: formation of quaternary and labile tertiary stereocenters. Org Lett (2014) 0.77
N-heterocyclic carbene-catalyzed internal redox reaction of alkynals: an efficient synthesis of allenoates. Org Lett (2012) 0.76
Theoretical studies on the regioselectivity of iridium-catalyzed 1,3-dipolar azide-alkyne cycloaddition reactions. J Org Chem (2014) 0.76
N-heterocyclic carbene catalyzed enantioselective α-fluorination of aliphatic aldehydes and α-chloro aldehydes: synthesis of α-fluoro esters, amides, and thioesters. Angew Chem Int Ed Engl (2014) 0.75
Stereoselective phosphine-catalyzed synthesis of highly functionalized diquinanes. Angew Chem Int Ed Engl (2010) 0.75
Cloning and comparative studies of seaweed trehalose-6-phosphate synthase genes. Mar Drugs (2010) 0.75
Siloxy alkynes in annulation reactions. Chem Rec (2014) 0.75
Highly chemoselective Pd-C catalytic hydrodechlorination leading to the highly efficient N-debenzylation of benzylamines. J Org Chem (2009) 0.75
Enantioselective formation of all-carbon quaternary stereocenters from indoles and tertiary alcohols bearing a directing group. Angew Chem Int Ed Engl (2014) 0.75
Preparation of 2-pyridone-containing tricyclic alkaloid derivatives as potential inhibitors of tumor cell proliferation by regioselective intramolecular N- and C-acylation of 2-pyridone. Chem Pharm Bull (Tokyo) (2005) 0.75
Characterization and fine mapping of RppQ, a resistance gene to southern corn rust in maize. Mol Genet Genomics (2007) 0.75
Geometry-invariant texture retrieval using a dual-output pulse-coupled neural network. Neural Comput (2011) 0.75
CuI catalyzed N-arylation of amide as a key step for the preparation of 3-aryl beta-carbolin-1-ones. Org Biomol Chem (2004) 0.75