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Studies of Australian Ascidians. I. Six New Lamellarin-Class Alkaloids From a Colonial Ascidian, Didemnum sp.
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Ueda Kirika,
Amaike Kazuma,
Maceiczyk Richard M.,
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Journal of the American Chemical Society. 2014 136(38). p.13226
Gold–silver catalyzed straightforward one pot synthesis of pyrano[3,4-b]pyrrol-7(1H)-ones
Delaye P.-O.,
Petrignet J.,
Thiery E., Thibonnet J.
Organic & Biomolecular Chemistry. 2017 15(35). p.7290
Ningalins, Pyrrole‐Bearing Metabolites Isolated from Didemnum spp. Synthesis and MDR‐Reversion Activity in Cancer Therapy
Segura‐Quezada Luis A.,
Hernández‐Velázquez Edson D.,
Corrales‐Escobosa Alma R.,
de León‐Solis Claudia, Solorio‐Alvarado César R.
Chemistry & Biodiversity. 2024 21(1).
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Bracegirdle Joe,
Robertson Luke P.,
Hume Paul A.,
Page Michael J.,
Sharrock Abigail V.,
Ackerley David F.,
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Journal of Natural Products. 2019 82(7). p.2000
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Axford Lorraine C.,
Holden Kate E.,
Hasse Katrin,
Banwell Martin G.,
Steglich Wolfgang,
Wagler Jörg, Willis Anthony C.
Australian Journal of Chemistry. 2008 61(2). p.80
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Zheng Kailu,
Zhuang Shiyi,
You Minqi,
Shu Wenming,
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ChemistrySelect. 2017 2(33). p.10762
1,5-Electrocyclization of conjugated azomethine ylides derived from 3-formyl chromene and N-alkyl amino acids/esters
Pravardhan Reddy E.,
Sumankumar A.,
Sridhar B.,
Hemasri Y.,
Jayaprakash Rao Y., Subba Reddy B. V.
Organic & Biomolecular Chemistry. 2017 15(36). p.7580
Modular Synthesis of Lamellarins via Regioselective Assembly of 3,4,5-Differentially Arylated Pyrrole-2-carboxylates
Komatsubara Masashi,
Umeki Teppei,
Fukuda Tsutomu, Iwao Masatomo
The Journal of Organic Chemistry. 2014 79(2). p.529
Pyrrolo[2,1-a]isoquinoline scaffolds for developing anti-cancer agents
García Maza Leidy J.,
Salgado Arturo Mendoza,
Kouznetsov Vladimir V., Meléndez Carlos M.
RSC Advances. 2024 14(3). p.1710
Total synthesis of lamellarins D, L, and N
Fujikawa Naotaka,
Ohta Takeshi,
Yamaguchi Tomohiro,
Fukuda Tsutomu,
Ishibashi Fumito, Iwao Masatomo
Tetrahedron. 2006 62(4). p.594
Handbook of Marine Natural Products (2012)
Synthesis of N -benzyl-des- D -ring lamellarin K via an acyl-Claisen/Paal-Knorr approach
Dittrich Nora,
Pilkington Lisa I.,
Leung Euphemia, Barker David
Tetrahedron. 2017 73(14). p.1881
Pyrrole‐Fused Benzoxazinones/Quinoxalinones: Molecular Dynamic Simulation, Antiproliferative and Antibacterial Activities
Selvendran Suresh,
Das Souvik,
Waidha Kamran,
Venkatesan Swathi,
Balamurali M. M.,
Basu Biswarup, Rajendran Saravanakumar
ChemistrySelect. 2021 6(40). p.10872
Marine natural products
Blunt John W.,
Copp Brent R.,
Munro Murray H. G.,
Northcote Peter T., Prinsep Mich�le R.
Natural Product Reports. 2005 22(1). p.15
Chromone Alkaloids: Structural Features, Distribution in Nature, and Biological Activity
Bondarenko S. P., Frasinyuk M. S.
Chemistry of Natural Compounds. 2019 55(2). p.201
Lamellarins as Inhibitors of P‐Glycoprotein‐Mediated Multidrug Resistance in a Human Colon Cancer Cell Line
Plisson Fabien,
Huang Xiao‐Cong,
Zhang Hua,
Khalil Zeinab, Capon Robert J.
Chemistry – An Asian Journal. 2012 7(7). p.1616
Investigation of the Dietary Preferences of Two Dorid Nudibranchs by Feeding-Choice Experiments and Chemical Analysis
Gris Lauren,
Battershill Christopher N., Prinsep Michele R.
Journal of Chemical Ecology. 2023 49(9-10). p.599
Acid-Promoted Redox-Annulation toward 1,2-Disubstituted-5,6-dihydropyrrolo[2,1-α]isoquinolines: Synthesis of the Lamellarin Core
Hou Guo-Quan,
Zhao Wenyan,
Deng Changjiang,
Dong Chunping,
Wang Cheli,
Liu Li, Li Jian
ACS Omega. 2022 7(42). p.37050
[3 + 2]-Annulation of pyridinium ylides with 1-chloro-2-nitrostyrenes unveils a tubulin polymerization inhibitor
Aksenov Alexander V.,
Arutiunov Nikolai A.,
Kirilov Nikita K.,
Aksenov Dmitrii A.,
Grishin Igor Yu.,
Aksenov Nicolai A.,
Wang Huifen,
Du Liqin,
Betancourt Tania,
Pelly Stephen C.,
Kornienko Alexander, Rubin Michael
Organic & Biomolecular Chemistry. 2021 19(33). p.7234
(2005)
Encyclopedia of Marine Natural Products (2014)
Database for Rapid Dereplication of Known Natural Products Using Data from MS and Fast NMR Experiments
Zani Carlos L., Carroll Anthony R.
Journal of Natural Products. 2017 80(6). p.1758
Bioactive natural Products (Part D) (2000)
Encyclopedia of Marine Natural Products (2014)
New lamellarin alkaloids from an unidentified ascidian from the Arabian Sea
Reddy M.Venkata Rami,
Faulkner D.John,
Venkateswarlu Y., Rao M.Rama
Tetrahedron. 1997 53(10). p.3457
Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions
Bellina Fabio, Rossi Renzo
Tetrahedron. 2006 62(31). p.7213
Assessing the drug-likeness of lamellarins, a marine-derived natural product class with diverse oncological activities
Chittchang Montakarn,
Paul Gleeson M.,
Ploypradith Poonsakdi, Ruchirawat Somsak
European Journal of Medicinal Chemistry. 2010 45(6). p.2165
Total Syntheses of Ningalin A, Lamellarin O, Lukianol A, and Permethyl Storniamide A Utilizing Heterocyclic Azadiene Diels−Alder Reactions
Boger Dale L.,
Boyce Christopher W.,
Labroli Marc A.,
Sehon Clark A., Jin Qing
Journal of the American Chemical Society. 1999 121(1). p.54
Anticancer Alkaloid Lamellarins Inhibit Protein Kinases
Baunbæk Dianne,
Trinkler Nolwenn,
Ferandin Yoan,
Lozach Olivier,
Ploypradith Poonsakdi,
Rucirawat Somsak,
Ishibashi Fumito,
Iwao Masatomo, Meijer Laurent
Marine Drugs. 2008 6(4). p.514
Encyclopedia of Marine Natural Products (2014)
Short and flexible route to 3,4-diarylpyrrole marine alkaloids: syntheses of permethyl storniamide A, ningalin B, and lamellarin G trimethyl ether
Iwao Masatomo,
Takeuchi Toshiro,
Fujikawa Naotaka,
Fukuda Tsutomu, Ishibashi Fumito
Tetrahedron Letters. 2003 44(24). p.4443
Toxicity and palatability of some British ascidians
Teo S. L.-M., Ryland J. S.
Marine Biology. 1994 120(2). p.297
Encyclopedia of Marine Natural Products (2014)
High-value compounds from the molluscs of marine and estuarine ecosystems as prospective functional food ingredients: An overview
Chakraborty Kajal, Joy Minju
Food Research International. 2020 137 p.109637
Biomimetic Total Synthesis of Lamellarin L by Coupling of Two Different Arylpyruvic Acid Units
Peschko Christian,
Winklhofer Christian, Steglich Wolfgang
Chemistry – A European Journal. 2000 6(7). p.1147
1,5-Electrocyclisation of azomethine ylides leading to pyrrolo[2,1-a]isoquinolines—concise construction of the lamellarin skeleton
Nyerges Miklós, Tőke László
Tetrahedron Letters. 2005 46(44). p.7531
Design and Synthesis of Lamellarin D Analogues Targeting Topoisomerase I
Ohta Takeshi,
Fukuda Tsutomu,
Ishibashi Fumito, Iwao Masatomo
The Journal of Organic Chemistry. 2009 74(21). p.8143
Synthesis of Non-Symmetrical 3,4-Diaryl-Substituted Pyrroles: Implementation for the Preparation of Lamellarin R
Zavala-Gómez Héctor,
Ramírez-Rodríguez Armando, Vázquez Alfredo
Journal of Chemical Research. 2017 41(12). p.677
Encyclopedia of Marine Natural Products (2014)
Synthesis of 5,6-dihydropyrrolo[2,1-a]isoquinolines via a TFA-promoted annulation of arylpropiolaldehydes and 1,2,3,4-tetrahydroisoquinolines
Zhang Yage,
Zhao Wenyan,
Hou Guoquan,
Liu Li, Li Jian
Tetrahedron Letters. 2023 120 p.154458
Total Syntheses of Lamellarin D and H. The First Synthesis of Lamellarin-Class Marine Alkaloids
Ishibashi Fumito,
Miyazaki Yuka, Iwao Masatomo
Tetrahedron. 1997 53(17). p.5951
The nature and role of pigments of marine invertebrates
Bandaranayake Wickramasinghe M.
Natural Product Reports. 2006 23(2). p.223
Marine Natural Products as Breast Cancer Resistance Protein Inhibitors
Cherigo Lilia,
Lopez Dioxelis, Martinez-Luis Sergio
Marine Drugs. 2015 13(4). p.2010
(2019)
(2020)
Combined Directedorthoand Remote Metalation−Suzuki Cross-Coupling Strategies. Efficient Synthesis of Heteroaryl-Fused Benzopyranones from BiarylO-Carbamates
James Clint A.,
Coelho Antonio Luiz,
Gevaert Matt,
Forgione Pat, Snieckus Victor
The Journal of Organic Chemistry. 2009 74(11). p.4094
Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms
Fan Hui,
Peng Jiangnan,
Hamann Mark T., Hu Jin-Feng
Chemical Reviews. 2008 108(1). p.264
Encyclopedia of Marine Natural Products (2014)
Handbook of Anticancer Drugs from Marine Origin (2015)
Total Synthesis of Lamellarins G, J, L, and Z Using One-Pot Halogen Dance/Negishi Coupling
Morii Kazuki,
Yasuda Yuto,
Morikawa Daiki,
Mori Atsunori, Okano Kentaro
The Journal of Organic Chemistry. 2021 86(19). p.13388
ChemInform Abstract: Studies of Australian Ascidians. Part 1. Six New Lamellarin‐Class Alkaloids from a Colonial Ascidian, Didemnum sp.
CARROLL A. R.,
BOWDEN B. F., COLL J. C.
ChemInform. 1993 24(30).
Multicomponent Reaction for the Synthesis of 5,6-Dihydropyrrolo[2,1-a]isoquinolines
Ghosh Aritra,
Kolle Shivalinga,
Barak Dinesh S.,
Kant Ruchir, Batra Sanjay
ACS Omega. 2019 4(24). p.20854
Toward “E‐Ring‐Free” Lamellarin Analogues: Synthesis and Preliminary Biological Evaluation
Rusanov Daniil A.,
Mutasim Alfadul Samah,
Portnyagina Ekaterina Yu.,
Silyanova Eugenia A.,
Kuznetsov Nikita A.,
Podpovetny Kirill E.,
Samet Alexander V.,
Semenov Victor V., Babak Maria V.
ChemBioChem. 2023 24(11).
Cytotoxicities and Structure–Activity Relationships of Natural and Unnatural Lamellarins toward Cancer Cell Lines
Chittchang Montakarn,
Batsomboon Paratchata,
Ruchirawat Somsak, Ploypradith Poonsakdi
ChemMedChem. 2009 4(3). p.457
Synthesis, structure–activity relationships, and mechanism of action of anti-HIV-1 lamellarin α 20-sulfate analogues
Kamiyama Haruka,
Kubo Yoshinao,
Sato Hironori,
Yamamoto Naoki,
Fukuda Tsutomu,
Ishibashi Fumito, Iwao Masatomo
Bioorganic & Medicinal Chemistry. 2011 19(24). p.7541
Facile and Divergent Synthesis of Lamellarins and Lactam‐Containing Derivatives with Improved Drug Likeness and Biological Activities
Theppawong Atiruj,
Ploypradith Poonsakdi,
Chuawong Pitak,
Ruchirawat Somsak, Chittchang Montakarn
Chemistry – An Asian Journal. 2015 10(12). p.2631
Efficient relay syntheses and assessment of the DNA-cleaving properties of the pyrrole alkaloid derivatives permethyl storniamide A, lycogalic acid A dimethyl ester, and the halitulin core
Fürstner Alois,
Krause Helga, Thiel Oliver R
Tetrahedron. 2002 58(32). p.6373
Base-Dependent Divergent Annulation of 4-Chloro-3-formylcoumarin and Tetrahydroisoquinoline: Application to the Synthesis of Isolamellarins and Hydroxypyrrolones
Vyasamudri Sameer, Yang Ding-Yah
The Journal of Organic Chemistry. 2019 84(6). p.3662
Bioactive Nitrogenous Metabolites from Ascidians
Namikoshi Michio, Wang Weifang
HETEROCYCLES. 2007 74(1). p.53
Contemporary Aspects of Boron: Chemistry and Biological Applications (2005)
Synthetic Approaches to the Lamellarins—A Comprehensive Review
Imbri Dennis,
Tauber Johannes, Opatz Till
Marine Drugs. 2014 12(12). p.6142
Biomimetische Synthese von Lamellarin‐G‐trimethylether
Heim Alexander,
Terpin Andreas, Steglich Wolfgang
Angewandte Chemie. 1997 109(1-2). p.158
APPROACHES TO THE SYNTHESIS OF THE LAMELLARINS AND RELATED NATURAL PRODUCTS. A REVIEW
Handy Scott T., Zhang Yanan
Organic Preparations and Procedures International. 2005 37(5). p.411
A Synthesis of Lamellarins via Regioselective Assembly of 1,2,3-Differentially Substituted 5,6-Dihydropyrrolo[2,1-a]Isoquinoline Core
Iwao Masatomo,
Fukuda Tsutomu, Sato Daichi
HETEROCYCLES. 2015 91(4). p.782
Palladium(II)-catalyzed cyclization of heterocyclic ketene aminals with (E)-ethyl 2,3-diiodoacrylates: selective synthesis of bicyclic pyrroles and bicyclic pyridones
Hu Ling,
Wang Kai-Min,
Zhao Min,
Lin Xin-Rong,
Zhu Hong-You,
Yan Sheng-Jiao, Lin Jun
Tetrahedron. 2014 70(30). p.4478
Recent Advances in Metal‐ and Organocatalyzed Asymmetric Functionalization of Pyrroles
Borah Biplob,
Dwivedi Kartikey Dhar, Chowhan L. Raju
Asian Journal of Organic Chemistry. 2021 10(11). p.2709
Domino Bischler–Napieralski – Michael Reaction and Oxidation – New Route to Coumarin‐Pyrrole‐Isoquinoline Fused Pentacycles
Mandrekar Ketan S.,
Kadam Hari K., Tilve Santosh G.
European Journal of Organic Chemistry. 2018 2018(47). p.6665
Synthesis of some new pyrrolyl dipyrazoles and pyrrolyl pyrazolyl isoxazoles and biological evaluation as antioxidants
Nagarjuna Ummadi,
Rekha Tamatam,
Sreenivasulu Thata,
Padmavathi Venkatapuram, Padmaja Adivireddy
Research on Chemical Intermediates. 2018 44(7). p.4375
Exploring the molecular basis for selective cytotoxicity of lamellarins against human hormone-dependent T47D and hormone-independent MDA-MB-231 breast cancer cells
Thipnate Poonsiri,
Chittchang Montakarn,
Thasana Nopporn,
Saparpakorn Patchreenart,
Ploypradith Poonsakdi, Hannongbua Supa
Monatshefte für Chemie - Chemical Monthly. 2011 142(1). p.97
(1996)
Alkaloids from Marine Invertebrates as Important Leads for Anticancer Drugs Discovery and Development
Imperatore Concetta,
Aiello Anna,
D'Aniello Filomena,
Senese Maria, Menna Marialuisa
Molecules. 2014 19(12). p.20391
(2022)
Secondary Metabolites of the Genus Didemnum: A Comprehensive Review of Chemical Diversity and Pharmacological Properties
Youssef Diaa T. A.,
Almagthali Hadeel,
Shaala Lamiaa A., Schmidt Eric W.
Marine Drugs. 2020 18(6). p.307
Storniamides A-D: Alkaloids from a Patagonian sponge Cliona sp.
Palermo Jorge A.,
Rodríguez Brasco María Florencia, Seldes Alicia M.
Tetrahedron. 1996 52(8). p.2727
Synthesis and Biological Activity of Lamellarin Alkaloids: An Overview
Iwao Masatomo,
Fukuda Tsutomu, Ishibashi Fumito
HETEROCYCLES. 2011 83(3). p.491
Marine Natural Products with P-Glycoprotein Inhibitor Properties
Lopez Dioxelis, Martinez-Luis Sergio
Marine Drugs. 2014 12(1). p.525
(2019)
5,6-Dihydropyrrolo[2,1-b]isoquinolines as scaffolds for synthesis of lamellarin analogues
Olsen Christian A.,
Parera Núria,
Albericio Fernando, Álvarez Mercedes
Tetrahedron Letters. 2005 46(12). p.2041
Synthesis of pyrrolocoumarins via Pd-catalyzed domino C–N coupling/hydroamination reactions
Ngo Thang Ngoc,
Akrawi Omer A.,
Dang Tuan Thanh,
Villinger Alexander, Langer Peter
Tetrahedron Letters. 2015 56(1). p.86
Gold-catalyzed formation of pyrrolo- and indolo-oxazin-1-one derivatives: The key structure of some marine natural products
Taskaya Sultan,
Menges Nurettin, Balci Metin
Beilstein Journal of Organic Chemistry. 2015 11 p.897
Efficient Synthesis of Ningalin C
Namsa-aid Anucha, Ruchirawat Somsak
Organic Letters. 2002 4(16). p.2633
Baculiferins A–O, O-sulfated pyrrole alkaloids with anti-HIV-1 activity, from the Chinese marine sponge Iotrochota baculifera
Fan Guotao,
Li Zelin,
Shen Shi,
Zeng Yi,
Yang Yishu,
Xu Minjuang,
Bruhn Torsten,
Bruhn Heike,
Morschhäuser Joachim,
Bringmann Gerhard, Lin Wenhan
Bioorganic & Medicinal Chemistry. 2010 18(15). p.5466
One-Pot Construction of 1-Phenylchromeno[3,4-b]pyrrol-4(3H)-one: Application to Total Synthesis of Ningalin B and a Pyrrolocoumarin-Based Electrochromic Switch
Wu Chun-Ku,
Weng Zhiqiang, Yang Ding-Yah
Organic Letters. 2019 21(13). p.5225
Applications of Friedel–Crafts reactions in total synthesis of natural products
Heravi Majid M.,
Zadsirjan Vahideh,
Saedi Pegah, Momeni Tayebeh
RSC Advances. 2018 8(70). p.40061
Synthesis of lamellarin R, lukianol A, lamellarin O and their analogues
Satyanarayana Iddum,
Yang Ding-Yah, Liou Teau-Jiuan
RSC Advances. 2020 10(70). p.43168
Ningalins A−D: Novel Aromatic Alkaloids from a Western Australian Ascidian of the Genus Didemnum
Kang Heonjoong, Fenical William
The Journal of Organic Chemistry. 1997 62(10). p.3254
A Novel Bromoindole Alkaloid from a Korean Colonial TunicateDidemnumsp.
Hahn Dongyup,
Kim Geum Jin,
Choi Hyukjae, Kang Heonjoong
Natural Product Sciences. 2015 21(4). p.278
Design, Synthesis and Structure-Activity Relationship Studies of Glycosylated Derivatives of Marine Natural Product Lamellarin D
Zheng Liuliu,
Gao Tingting,
Ge Zhiwei,
Ma Zhongjun,
Xu Jinzhong,
Ding Wanjing, Shen Li
European Journal of Medicinal Chemistry. 2021 214 p.113226
Rotational Energy Barrier around the C1–C11 Single Bond in Lamellarins: A Study by Variable-Temperature NMR
Iwao Masatomo,
Fukuda Tsutomu,
Itoyama Ryosuke, Minagawa Terufusa
HETEROCYCLES. 2014 88(2). p.1121
Biomimetic Synthesis of Lamellarin G. Trimethyl Ether
Heim Alexander,
Terpin Andreas, Steglich Wolfgang
Angewandte Chemie International Edition in English. 1997 36(1-2). p.155
Isolation, Bioactivities, and Synthesis of Lamellarin Alkaloids: A Review
Duc Dau Xuan, Quoc Nguyen Van
Current Organic Chemistry. 2022 26(10). p.961
Convergent Total Syntheses of the Pentacyclic Lamellarins K, T, U and W via the Addition of Azomethine Ylides to Tethered Tolans
G. Banwell Martin
HETEROCYCLES. 2012 84(2). p.1141
