Related references
Note: Only part of the references are listed.Total Syntheses of the 3H-Pyrrolo[2,3-c]quinolone-Containing Alkaloids Marinoquinolines A-F, K, and Aplidiopsamine A Using a Palladium-Catalyzed Ullmann Cross-Coupling/Reductive Cyclization Pathway
Benoit Bolte et al.
JOURNAL OF ORGANIC CHEMISTRY (2020)
Formation of 6-Azaindoles by Intramolecular Diels-Alder Reaction of Oxazoles and Total Synthesis of Marinoquinoline A
Mana Osano et al.
ORGANIC LETTERS (2020)
Synthesis and Investigation of the Abiotic Formation of Pyonitrins A-D
Rahul D. Shingare et al.
ORGANIC LETTERS (2020)
TosMIC: A Powerful Synthon for Cyclization and Sulfonylation
Kapil Kumar
CHEMISTRYSELECT (2020)
Synthesis, Crystal Structure and Anti-leukemic Activity of 4-{4-[(4-(2-Oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidin-1-yl)benzyl]}-3-phenyl-3H-pyrrolo[2,3-c]quinoline
Jean Guillon et al.
JOURNAL OF CHEMICAL CRYSTALLOGRAPHY (2019)
Synthesis of 3 H-Pyrrolo[2,3-c]quinoline by Sequential I2-Promoted Cyclization/Staudinger/Aza-Wittig/Dehydroaromatization Reaction
Fakai Zou et al.
SYNLETT (2019)
Functionalized Chitosan-Carbon Dots: A Fluorescent Probe for Detecting Trace Amount of Water in Organic Solvents
Shweta Pawar et al.
ACS OMEGA (2019)
Pyonitrins A-D: Chimeric Natural Products Produced by Pseudomonas protegens
Emily Mevers et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)
Tandem Cyclization-Annulation of α-Acidic Isocyanides with 2-Methyleneaminochalcones: Synthesis of Pyrrolo[2,3-c]quinoline Derivatives
Jinhuan Dong et al.
ADVANCED SYNTHESIS & CATALYSIS (2019)
Selective Sensing of Iron by Pyrrolo[2,3-c]Quinolines
Togiti Uday Kumar et al.
JOURNAL OF FLUORESCENCE (2019)
An overview on synthetic entries to tetrahydro-β-carbolines
Pradipta Maity et al.
TETRAHEDRON (2019)
Metal-Enhanced Fluorescence Study in Aqueous Medium by Coupling Gold Nanoparticles and Fluorophores Using a Bilayer Vesicle Platform
Shweta Pawar et al.
ACS OMEGA (2019)
Regioselective ring expansion followed by H-shift of 3-ylidene oxindoles: a convenient synthesis of N-substituted/un-substituted pyrrolo[2,3-c] quinolines and marinoquinolines
Gopathi Ramu et al.
RSC ADVANCES (2019)
The Palladium-Catalyzed Ullmann Cross-Coupling Reaction: A Modern Variant on a Time-Honored Process
Faiyaz Khan et al.
ACCOUNTS OF CHEMICAL RESEARCH (2018)
Discovery of Marinoquinolines as Potent and Fast-Acting Plasmodium falciparum Inhibitors with in Vivo Activity
Anna Caroline Campos Aguiar et al.
JOURNAL OF MEDICINAL CHEMISTRY (2018)
Synthesis of 4-Substituted Pyrrolo[2,3-c]quinolines via Microwave-Assisted C-N Bond Formation
Thirupathi Reddy Penjada et al.
CHEMISTRYSELECT (2018)
Divergent Synthesis of Quinoline Derivatives via [5+1] Annulation of 2-Isocyanochalcones with Nitroalkanes
Lan Bao et al.
ADVANCED SYNTHESIS & CATALYSIS (2018)
Synthesis of Multi-Substituted Pyrrole Derivatives Through [3+2] Cycloaddition with Tosylmethyl Isocyanides (TosMICs) and Electron-Deficient Compounds
Zhengning Ma et al.
MOLECULES (2018)
Bicyclization of Azomethine Ylide: Access to Highly Functionalized 3H-Pyrrolo[2,3-c]quinolines
Yang Men et al.
ORGANIC LETTERS (2017)
FRET-Mediated Zn2+ Sensing in Aqueous Micellar Solution: Application in Cellular Imaging and Molecular Logic Gate
Shweta V. Pawar et al.
CHEMISTRYSELECT (2017)
Zinc(II) Ion Sensing in Aqueous Micellar Solution Using Modified Bipyridine-Based Turn-On Fluorescent Probes and its Application in Bioimaging
Shweta Pawar et al.
CHEMPLUSCHEM (2016)
Exploring the ocean for new drug developments: Marine pharmacology
Harshad Malve
JOURNAL OF PHARMACY AND BIOALLIED SCIENCES (2016)
Recent advancement of Ullmann-type coupling reactions in the formation of C-C bond
Shovan Mondal
CHEMTEXTS (2016)
Previously Uncultured Marine Bacteria Linked to Novel Alkaloid Production
Eun Ju Choi et al.
CHEMISTRY & BIOLOGY (2015)
Selective detection of fluoride using fused quinoline systems: effect of pyrrole
Mahesh Akula et al.
RSC ADVANCES (2015)
Electrophilic Trifluoromethylation by Use of Hypervalent Iodine Reagents
Julie Charpentier et al.
CHEMICAL REVIEWS (2015)
Development of a Bronsted Acid-Promoted Arene-Ynamide Cyclization toward the Total Syntheses of Marinoquinolines A and C and Aplidiopsamine A
Yousuke Yamaoka et al.
JOURNAL OF ORGANIC CHEMISTRY (2015)
Applications of Bartoli indole synthesis
Giuseppe Bartoli et al.
CHEMICAL SOCIETY REVIEWS (2014)
Selection of boron reagents for Suzuki-Miyaura coupling
Alastair J. J. Lennox et al.
CHEMICAL SOCIETY REVIEWS (2014)
New class of antitubercular compounds: synthesis and anti-tubercular activity of 4-substituted pyrrolo[2,3-c]quinolines
Mahesh Akula et al.
MONATSHEFTE FUR CHEMIE (2014)
Selective Zn2+ sensing using a modified bipyridine complex
Mahesh Akula et al.
RSC ADVANCES (2014)
Recent advances in the synthesis of quinolines: a review
Shraddha M. Prajapati et al.
RSC ADVANCES (2014)
Extending the Utility of the Bartoli Indolization: Synthesis of Marinoquinolines C and E
Ashley C. Lindsay et al.
SYNLETT (2013)
Selective synthesis of 4,5-dihydroimidazo- and imidazo[1,5-a] quinoxalines via modified Pictet-Spengler reaction
Akhilesh Kumar Verma et al.
TETRAHEDRON LETTERS (2013)
Pd-Catalyzed Imine Cyclization: Synthesis of Antimalarial Natural Products Aplidiopsamine A, Marinoquinoline A, and Their Potential Hybrid NCLite-M1
Jyoti P. Mahajan et al.
ORGANIC LETTERS (2012)
Biomimetic Synthesis and Biological Evaluation of Aplidiopsamine A
Joseph D. Panarese et al.
ORGANIC LETTERS (2012)
Divergent total synthesis of the natural antimalarial marinoquinolines A, B, C, E and unnatural analogues
Cristiane Storck Schwalm et al.
TETRAHEDRON LETTERS (2012)
Concise total syntheses of Marinoquinolines A-C
Lijun Ni et al.
TETRAHEDRON LETTERS (2012)
Total Synthesis of Marinoquinoline A Using a Palladium(0)-Catalyzed Ullmann Cross-Coupling Reaction
Xinghua Ma et al.
ASIAN JOURNAL OF ORGANIC CHEMISTRY (2012)
Evolution and Synthetic Applications of the Heck-Matsuda Reaction: The Return of Arenediazonium Salts to Prominence
Jason G. Taylor et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2011)
Marinoquinolines A-F, Pyrroloquinolines from Ohtaekwangia kribbensis (Bacteroidetes)
Patrick W. Okanya et al.
JOURNAL OF NATURAL PRODUCTS (2011)
Trigonoines A and B, two novel alkaloids from the leaves of Trigonostemon lii
Shi-Fei Li et al.
TETRAHEDRON LETTERS (2011)
Aplidiopsamine A, an Antiplasmodial Alkaloid from the Temperate Australian Ascidian, Aplidiopsis confluata
Anthony R. Carroll et al.
JOURNAL OF ORGANIC CHEMISTRY (2010)
Structure-activity relationship of antiparasitic and cytotoxic indoloquinoline alkaloids, and their tricyclic and bicyclic analogues
Gitte Van Baelen et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2009)
From Nature to Drug Discovery: The Indole Scaffold as a 'Privileged Structure'
Fernando Rodrigues de Sa Alves et al.
MINI-REVIEWS IN MEDICINAL CHEMISTRY (2009)
Synthesis of 5-methyl-5H-pyrrolo[2,3-c]quinoline and 4-methyl-4H-pyrrolo[2,3-c]isoquinoline: two new unnatural D-ring stripped isomers of the cryptolepine series
Gitte Van Baelen et al.
ARKIVOC (2009)
Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
Ruben Martin et al.
ACCOUNTS OF CHEMICAL RESEARCH (2008)
Acetylcholinesterase-Inhibiting Activity of Pyrrole Derivatives from a Novel Marine Gliding Bacterium, Rapidithrix thailandica
Yutthapong Sangnoi et al.
MARINE DRUGS (2008)
Rapidithrix thailandica gen. nov., sp nov., a marine gliding bacterium isolated from samples collected from the Andaman sea, along the southern coastline of Thailand
Pornpoj Srisukchayakul et al.
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY (2007)
Palladium-catalyzed, modular synthesis of highly functionalized indoles and tryptophans by direct annulation of substituted o-haloanilines and aldehydes
Yanxing Jia et al.
JOURNAL OF ORGANIC CHEMISTRY (2006)
Flexible, palladium-catalyzed indole and azaindole synthesis by direct annulation of chloroanilines and chloroaminopyridines with ketones
M Nazare et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2004)
One-step synthesis of 3-aryl- and 3,4-diaryl-(1H)-pyrroles using tosylmethyl isocyanide (TOSMIC)
ND Smith et al.
ORGANIC LETTERS (2002)
Share Paper
