Related references
Note: Only part of the references are listed.Iron Catalysis in Reduction and Hydrometalation Reactions
Duo Wei et al.
CHEMICAL REVIEWS (2019)
Development of Synthetic Methodologies via Catalytic Enantioselective Synthesis of 3,3-Disubstituted Oxindoles
Zhong-Yan Cao et al.
ACCOUNTS OF CHEMICAL RESEARCH (2018)
Gold(I)-Catalyzed and Nucleophile-Guided Ligand-Directed Divergent Synthesis
Yen-Chun Lee et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2018)
Thiyl radical promoted chemo- and regioselective oxidation of C=C bonds using molecular oxygen via iron catalysis
Baojian Xiong et al.
GREEN CHEMISTRY (2018)
Enantioselective N-Heterocyclic Carbene-Catalyzed Synthesis of Spirocyclic Oxindole-benzofuroazepinones
Zhong-Hua Gao et al.
JOURNAL OF ORGANIC CHEMISTRY (2018)
Synthesis of isochromans via Fe(OTf)(2)-catalyzed Oxa-Pictet-Spengler cyclization
Jimei Zhou et al.
TETRAHEDRON (2018)
Synthesis of spiroindolone scaffolds by Pictet-Spengler spirocyclisation using β-cyclodextrin-SO3H as a recyclable catalyst
Tukaram D. Urmode et al.
TETRAHEDRON (2017)
Diversity-Oriented Synthesis of Oxacyclic Spirooxindole Derivatives through Ring-Closing Enyne Metathesis and Intramolecular Pauson-Khand (2+2+1) Cyclization of Oxindole Enynes
Satheeshkumar Reddy Kandimalla et al.
ADVANCED SYNTHESIS & CATALYSIS (2017)
Direct Asymmetric Aza-Vinylogous-Type Michael Additions of Nitrones from Isatins to Nitroalkenes
Gu Zhan et al.
CHEMISTRY-A EUROPEAN JOURNAL (2017)
Diastereo- and Enantioselective Construction of Dihydroisocoumarin-Based Spirooxindole Frameworks via Organocatalytic Tandem Reactions
Jia-Le Wu et al.
ADVANCED SYNTHESIS & CATALYSIS (2016)
Discovery of SOAT2 inhibitors from synthetic small molecules
Keisuke Kobayashi et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2016)
Spiroindolone NITD609 is a novel antimalarial drug that targets the P-type ATPase PfATP4
Helen Turner
FUTURE MEDICINAL CHEMISTRY (2016)
Direct Formation of Oxocarbenium Ions under Weakly Acidic Conditions: Catalytic Enantioselective Oxa-Pictet-Spengler Reactions
Chenfei Zhao et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2016)
Oxidative diversification of amino acids and peptides by small-molecule iron catalysis
Thomas J. Osberger et al.
NATURE (2016)
Catalytic asymmetric hetero-Diels-Alder reactions of enones with isatins to access functionalized spirooxindole tetrahydropyrans: scope, derivatization, and discovery of bioactives
Hai-Lei Cui et al.
ORGANIC & BIOMOLECULAR CHEMISTRY (2016)
Regio- and Enantioselective Aza-Diels-Alder Reactions of 3-Vinylindoles: A Concise Synthesis of the Antimalarial Spiroindolone NITD609
Haifeng Zheng et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2015)
Iron Catalysis in Organic Synthesis
Ingmar Bauer et al.
CHEMICAL REVIEWS (2015)
Stereoselective Synthesis of 1-Methyl-3′,4′,5′,6′-tetrahydrospiro[indoline-3,2′-pyran]-2-one Derivatives via Prins Cyclization
Krishna Damera et al.
JOURNAL OF ORGANIC CHEMISTRY (2015)
Iron-promoted C-C bond formation in the total synthesis of natural products and drugs
Julien Legros et al.
NATURAL PRODUCT REPORTS (2015)
Stereoselective Total Synthesis of KAE609 via Direct Catalytic Asymmetric Alkynylation to Ketimine
Hisashi Takada et al.
ORGANIC LETTERS (2015)
Asymmetric Triple Relay Catalysis: Enantioselective Synthesis of Spirocyclic Indolines through a One-Pot Process Featuring an Asymmetric 6π Electrocyclization
Xiao-Ping Yin et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2014)
Spiroindolone That Inhibits PfATPase4 Is a Potent, Cidal Inhibitor of Toxoplasma gondii Tachyzoites In Vitro and In Vivo
Ying Zhou et al.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2014)
A First-in-Human Randomized, Double-Blind, Placebo-Controlled, Single- and Multiple-Ascending Oral Dose Study of Novel Antimalarial Spiroindolone KAE609 (Cipargamin) To Assess Its Safety, Tolerability, and Pharmacokinetics in Healthy Adult Volunteers
F. Joel Leong et al.
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY (2014)
SAR405838: An Optimized Inhibitor of MDM2-p53 Interaction That Induces Complete and Durable Tumor Regression
Shaomeng Wang et al.
CANCER RESEARCH (2014)
Diastereo- and Enantioselective Construction of a Bispirooxindole Scaffold Containing a Tetrahydro-β-carboline Moiety through an Organocatalytic Asymmetric Cascade Reaction
Wei Dai et al.
CHEMISTRY-A EUROPEAN JOURNAL (2014)
Organocatalytic Asymmetric Assembly Reactions: Synthesis of Spirooxindoles via Organocascade Strategies
Daojuan Cheng et al.
ACS CATALYSIS (2014)
Recent Advances in Asymmetric Organocatalytic Construction of 3,3′-Spirocyclic Oxindoles
Liang Hong et al.
ADVANCED SYNTHESIS & CATALYSIS (2013)
One-Pot Tandem Approach to Spirocyclic Oxindoles Featuring Adjacent Spiro-Stereocenters
Yun-Lin Liu et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)
Catalytic Enantioselective Formal Hetero-Diels-Alder Reactions of Enones with Isatins to Give Spirooxindole Tetrahydropyranones
Hai-Lei Cui et al.
CHEMISTRY-A EUROPEAN JOURNAL (2013)
DRUG DISCOVERY Diversifying complexity
Indrajeet Sharma et al.
NATURE CHEMISTRY (2013)
Zn(OTf)2-catalysed indolylation and pyrrolylation of isatins: Efficient synthesis and biochemical assay of 3,3-di(heteroaryl)oxindoles
C. Praveen et al.
JOURNAL OF CHEMICAL SCIENCES (2013)
Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks
Girija S. Singh et al.
CHEMICAL REVIEWS (2012)
Antiparasitic agents: new drugs on the horizon
Pascal Maeser et al.
CURRENT OPINION IN PHARMACOLOGY (2012)
Mechanistic Study of the Spiroindolones: A New Class of Antimalarials
Bin Zou et al.
MOLECULES (2012)
An Easy Entry to Optically Active Spiroindolinones: Chiral Bronsted Acid-Catalysed Pictet-Spengler Reactions of Isatins
Sara Duce et al.
ADVANCED SYNTHESIS & CATALYSIS (2011)
Rhodium(II) acetate-catalyzed stereoselective synthesis, SAR and anti-HIV activity of novel oxindoles bearing cyclopropane ring
Garima Kumari et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2011)
Direct Nucleophilic SN1-Type Reactions of Alcohols
Enrico Emer et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2011)
Synthesis of Oxacycles Employing the Oxa-Pictet-Spengler Reaction: Recent Developments and New Prospects
Enrique L. Larghi et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2011)
Enantioselective Pictet-Spengler reactions of isatins for the synthesis of spiroindolones
Joseph J. Badillo et al.
TETRAHEDRON LETTERS (2011)
A regio- and stereoselective 1,3-dipolar cycloaddition for the synthesis of novel spiro-pyrrolothiazolyloxindoles and their antitubercular evaluation
Pitchaimani Prasanna et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2010)
Synthesis and Antitumor Effect in Vitro and in Vivo of Substituted 1,3-Dihydroindole-2-ones
Mette K. Christensen et al.
JOURNAL OF MEDICINAL CHEMISTRY (2010)
Spirotetrahydro β-Carbolines (Spiroindolones): A New Class of Potent and Orally Efficacious Compounds for the Treatment of Malaria
Bryan K. S. Yeung et al.
JOURNAL OF MEDICINAL CHEMISTRY (2010)
Spiroindolones, a Potent Compound Class for the Treatment of Malaria
Matthias Rottmann et al.
SCIENCE (2010)
BISMUTH TRIFLATE AS A SAFE AND READILY HANDLED SOURCE OF TRIFLIC ACID: APPLICATION TO THE OXA-PICTET-SPENGLER REACTION
Benaissa Bouguerne et al.
SYNTHETIC COMMUNICATIONS (2010)
Catalytic Functionalization of Indoles in a New Dimension
Marco Bandini et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2009)
Efficient synthesis of 3,3-diheteroaromatic oxindole analogues and their in vitro evaluation for spermicidal potential
Priyankar Paira et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2009)
Stereoselective Synthesis of Spirocyclic Oxindoles via Prins Cyclizations
M. Paola Castaldi et al.
ORGANIC LETTERS (2009)
Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products
Barry M. Trost et al.
SYNTHESIS-STUTTGART (2009)
Scandium triflate-catalyzed intramolecular Friedel-Crafts acylation with Meldrum's acids: insight into the mechanism
Eric Fillion et al.
TETRAHEDRON (2009)
The oxa-Pictet-Spengler reaction: A highlight on the different efficiency between isochroman and phthalan or homoisochroman derivative syntheses
Marcella Guiso et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2008)
Bismuth triflate-catalyzed oxa- and thia-Pictet-Spengler reactions:: access to iso- and isothio-chroman compounds
Christian Lherbet et al.
TETRAHEDRON LETTERS (2008)
Biomimetic synthesis of the tetracyclic core of berkelic acid
Jingye Zhou et al.
ORGANIC LETTERS (2007)
Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents
Chris V. Galliford et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2007)
Efficient entry to diversely functionalized spirocyclic oxindoles from isatins through carbonyl-addition/cyclization reaction sequences
B Alcaide et al.
JOURNAL OF ORGANIC CHEMISTRY (2006)
Zeolite-catalyzed simple synthesis of isochromans via the oxa-Pictet-Spengler reaction
A Hegedus et al.
ORGANIC & BIOMOLECULAR CHEMISTRY (2006)