Relevant bibliographies by topics / Carbazole Alkaloids

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Carbazole Alkaloids'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Carbazole Alkaloids.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Carbazole Alkaloids"

1

Chakraborty, M. "Mumunine - A New Carbazole Alkaloid from Murraya koenigii (Linn.) Spreng." Journal of Scientific Research 12, no. 4 (September 1, 2020): 665–72. http://dx.doi.org/10.3329/jsr.v12i4.45499.

Full text
Abstract:
The plant Murraya koenigii, commonly known as curry leaf tree is a rich source of carbazole alkaloids. A number of monomeric as well as dimeric carbazoles with C13, C18 and C23 skeleton have been isolated from the plant. In my present work, a new carbazole alkaloid, designated as mumunine, was isolated from the bark of Murraya koenigii (Linn) Spreng, along with a known carbazole alkaloid, viz. mahanimbine. The structure of the new alkaloid 1 was elucidated on the basis of 1D and 2D NMR spectral data analysis. In this paper, the isolation and structure elucidation of the new compound will be discussed in detail.
APA, Harvard, Vancouver, ISO, and other styles
2

Kumar, V., J. Reisch, and A. Wickramasinghe. "Glycomaurin and Glycomaurrol, New Carbazole Alkaloids From Glycosmis mauritiana (Rutaceae) Bark." Australian Journal of Chemistry 42, no. 8 (1989): 1375. http://dx.doi.org/10.1071/ch9891375.

Full text
Abstract:
The stem bark of Glycosmis mauritiana contained the acridone alkaloids noracronycine and des-N- methylacronycine, and two new carbazole alkaloids, 3,3,10-trimethyl-3,7-dihydropyrano[2,3-c] carbazole (glycomaurin) and 6-methyl-4-(3′-methylbut-2′-enyl)carbazol-3-ol (glycomaurrol), whose structures were confirmed by synthesis and by cyclization to dihydroglycomaurin respectively. Glycomaurin has a ring system which has not been previously found in nature.
APA, Harvard, Vancouver, ISO, and other styles
3

Yang, Jing-Hua, Xin-Yi Wang, Yi-Ping Zhou, Rong Lu, Chin-Ho Chen, Meng-Han Zhang, Yung-Yi Cheng, Susan L. Morris-Natschke, Kuo-Hsiung Lee, and Yun-Song Wang. "Carbazole Alkaloids from Clausena anisum-olens: Isolation, Characterization, and Anti-HIV Evaluation." Molecules 25, no. 1 (December 26, 2019): 99. http://dx.doi.org/10.3390/molecules25010099.

Full text
Abstract:
Two new carbazole alkaloids (1,2) and six known carbazole alkaloids (3–8) were isolated from Clausena anisum-olens. Their structures were elucidated based on extensive spectroscopic analysis. All isolated compounds (1–8) were evaluated for their anti-HIV effects on virus replication in MT-4 lymphocytes infected by HIV-1NL4-3 Nanoluc-sec virus, and new carbazole alkaloid 1 exhibited anti-HIV activity with an EC50 value of 2.4 μg/mL and SI of 7.1.
APA, Harvard, Vancouver, ISO, and other styles
4

Kobayashi, Masaya, and Tomohisa Kuzuyama. "Recent Advances in the Biosynthesis of Carbazoles Produced by Actinomycetes." Biomolecules 10, no. 8 (August 5, 2020): 1147. http://dx.doi.org/10.3390/biom10081147.

Full text
Abstract:
Structurally diverse carbazole alkaloids are valuable due to their pharmaceutical properties and have been isolated from nature. Experimental knowledge on carbazole biosynthesis is limited. The latest development of in silico analysis of the biosynthetic gene clusters for bacterial carbazoles has allowed studies on the biosynthesis of a carbazole skeleton, which was established by sequential enzyme-coupling reactions associated with an unprecedented carbazole synthase, a thiamine-dependent enzyme, and a ketosynthase-like enzyme. This review describes the carbazole biosynthetic mechanism, which includes a key step in enzymatic formation of a tricyclic carbazole skeleton, followed by modifications such as prenylation and hydroxylation in the skeleton.
APA, Harvard, Vancouver, ISO, and other styles
5

Ma, Xiaoli, Hongwei Chen, Sisi Zhu, Pengfei Tu, and Yong Jiang. "Trimeric and Dimeric Carbazole Alkaloids from Murraya microphylla." Molecules 26, no. 18 (September 20, 2021): 5689. http://dx.doi.org/10.3390/molecules26185689.

Full text
Abstract:
Seventeen new carbazole alkaloid derivatives, including a trimeric carbazole racemate, (±)-microphyltrine A (1), 15 dimeric carbazole racemates, (±)-microphyldines A–O (2–16), and a C-6–C-3″-methyl-linked dimeric carbazole, microphyldine P (17), were isolated from the leaves and stems of Murraya microphylla (Merr. et Chun) Swingle. The structures of the new compounds were elucidated on the basis of HRESIMS and NMR data analysis. The optically pure isomers of these isolated carbazole alkaloids were obtained by chiral HPLC separation and their absolute configurations were determined by electronic circular dichroism (ECD) data analysis.
APA, Harvard, Vancouver, ISO, and other styles
6

Mandal, Suvra, Anupam Nayak, Samir K. Banerjee, Julie Banerji, and Avijit Banerji. "A New Carbazole Alkaloid from Murraya koenigii Spreng (Rutaceae)." Natural Product Communications 3, no. 10 (October 2008): 1934578X0800301. http://dx.doi.org/10.1177/1934578x0800301019.

Full text
Abstract:
A new carbazole alkaloid (kurryam) oxygenated at the 4-position, hitherto unknown among carbazole alkaloids, has been isolated from the seeds of an Indian medicinal plant, Murraya koenigii (Rutaceae). The structure has been established as 4-hydroxy-(2′,2′,3)-trimethyl-(6,7)-dimethoxy pyranocarbazole from extensive 2D NMR spectral studies. In addition, two known carbazole alkaloids, (2′,2′,3)-trimethyl 6-methoxy pyranocarbazole and (2′,2′,3)-trimethyl 6-hydroxy pyranocarbazole were isolated from the seeds of the same plant, of which (2′,2′,3)-trimethyl 6-methoxy pyranocarbazole exhibited significant antidiarrhoeal activity, as also did the new compound.
APA, Harvard, Vancouver, ISO, and other styles
7

Chakraborty, Mumu, Sudipta Saha, and Sibabrata Mukhapadhyay. "Murrayakoeninol- A New Carbazole Alkaloid from Murraya Koenigii (Linn) Spreng." Natural Product Communications 4, no. 3 (March 2009): 1934578X0900400. http://dx.doi.org/10.1177/1934578x0900400309.

Full text
Abstract:
A new carbazole alkaloid, designated as murrayakoeninol, was isolated from the leaves of Murraya koenigii (Linn) Spreng, along with four known carbazole alkaloids, viz. mahanimbine, koenimbine, O-methylmurrayamine-A and murrayazolinine and one from the bark viz. girinimbine. The structure of the new alkaloid 1 was elucidated on the basis of 2D NMR spectral analysis and chemical reactions.
APA, Harvard, Vancouver, ISO, and other styles
8

Chakraborty, M. "Identification of Naturally Occurring Carbazole Alkaloids Isolated from <i>Murraya koenigii</i> and <i>Glycosmis pentaphylla</i> by the Preparation of HPLC Fingerprint." Journal of Scientific Research 14, no. 1 (January 1, 2022): 289–300. http://dx.doi.org/10.3329/jsr.v14i1.53526.

Full text
Abstract:
The plants Murraya koenigii and Glycosmis pentaphylla are rich sources of different carbazole alkaloids. A number of monomeric carbazole alkaloids with C13, C18, and C23 carbon frames and a good number of dimeric carbazole alkaloids were isolated from these two plants. Scientists are still working on these two plants in search of more and more novel compounds. Many of these alkaloids have potential biological activities. Scientists have determined the structures of these compounds by detailed analysis of spectral data like UV, IR, Mass,1H NMR, and 13C NMR (1D and 2D). These procedures require expertise in spectral data analysis and huge time, and also these instruments are very costly. In this paper, I report the preparation of the HPLC fingerprint of some known carbazole alkaloids. These HPLC data will be helpful in quick and unambiguous identification of the natural products.
APA, Harvard, Vancouver, ISO, and other styles
9

Moody, Christopher J. "Synthesis of Carbazole Alkaloids." Synlett 1994, no. 09 (1994): 681–88. http://dx.doi.org/10.1055/s-1994-22975.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Bergman, J., and B. Pelcman. "Synthesis of carbazole alkaloids." Pure and Applied Chemistry 62, no. 10 (January 1, 1990): 1967–76. http://dx.doi.org/10.1351/pac199062101967.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Carbazole Alkaloids"

1

Hesse, Ronny, Anne Jäger, Arndt W. Schmidt, and Hans-Joachim Knölker. "Palladium(II)-catalysed total synthesis of naturally occurring pyrano[3,2-a]carbazole and pyrano[2,3-b]carbazole alkaloids." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-149135.

Full text
Abstract:
Seven naturally occurring pyranocarbazole alkaloids (pyrayafoline A–E, O-methylmurrayamine A and O-methylmahanine) have been obtained by total synthesis using a palladium(II)-catalysed oxidative cyclisation of a diarylamine to an orthogonally diprotected 2,7-dihydroxycarbazole as key step.
APA, Harvard, Vancouver, ISO, and other styles
2

Scott, Tricia L. "Palladium-catalyzed synthesis of carbazole derivatives and formal total syntheses of several naturally occurring carbazole alkaloids." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2075.

Full text
Abstract:
Thesis (Ph. D.)--West Virginia University, 2001.
Title from document title page. Document formatted into pages; contains x, 83 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 75-78).
APA, Harvard, Vancouver, ISO, and other styles
3

Knott, Kerstin. "Iron-mediated Synthesis of the Antiostatins." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-ds-1237582907592-42405.

Full text
Abstract:
Within this thesis the first total syntheses of eight biologically active natural products from the family of carbazole alkaloids, antiostatins A1 to A4 and B2 to B5, were established. Spectroscopic data of the synthesised natural products are in good agreement with the isolated antiostatins from Streptomyces cyaneus 2007-SV1, which confirms the molecular structures assigned to the natural products. The total synthesis of the antiostatins A1 to A4 and B2 to B5 were achieved employing the iron-mediated synthesis to form the carbazole nucleus from a cyclohexadienylium iron salt and appropriate arylamines. This transition metal-mediated approach could be applied to all antiostatins in excellent yields. The antiostatins A1-4 and B2-5 represent the first carbazole alkaloids with an acetamide or substituted biuret chain. Introduction of the sophisticated substituents proceeded selectively on C-4 in high yields. Antiostatins A1 to A4 and B2 to B5 could be synthesised over eight steps from a tricarbonyliron-coordinated cyclohexadienylium salt. The overall yields are in the range of 31 – 63%.
APA, Harvard, Vancouver, ISO, and other styles
4

Gassner, Cemena, Ronny Hesse, Arndt W. Schmidt, and Hans-Joachim Knölker. "Total synthesis of the cyclic monoterpenoid pyrano[3,2-a]carbazole alkaloids derived from 2-hydroxy-6-methylcarbazole." Royal Society of Chemistry, 2014. https://tud.qucosa.de/id/qucosa%3A28532.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Knott, Kerstin. "Iron-mediated Synthesis of the Antiostatins." Doctoral thesis, Technische Universität Dresden, 2008. https://tud.qucosa.de/id/qucosa%3A24053.

Full text
Abstract:
Within this thesis the first total syntheses of eight biologically active natural products from the family of carbazole alkaloids, antiostatins A1 to A4 and B2 to B5, were established. Spectroscopic data of the synthesised natural products are in good agreement with the isolated antiostatins from Streptomyces cyaneus 2007-SV1, which confirms the molecular structures assigned to the natural products. The total synthesis of the antiostatins A1 to A4 and B2 to B5 were achieved employing the iron-mediated synthesis to form the carbazole nucleus from a cyclohexadienylium iron salt and appropriate arylamines. This transition metal-mediated approach could be applied to all antiostatins in excellent yields. The antiostatins A1-4 and B2-5 represent the first carbazole alkaloids with an acetamide or substituted biuret chain. Introduction of the sophisticated substituents proceeded selectively on C-4 in high yields. Antiostatins A1 to A4 and B2 to B5 could be synthesised over eight steps from a tricarbonyliron-coordinated cyclohexadienylium salt. The overall yields are in the range of 31 – 63%.
APA, Harvard, Vancouver, ISO, and other styles
6

Gassner, Cemena, Ronny Hesse, Arndt W. Schmidt, and Hans-Joachim Knölker. "Total synthesis of the cyclic monoterpenoid pyrano[3,2-a]carbazole alkaloids derived from 2-hydroxy-6-methylcarbazole." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-160632.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Shi, Chongsheng. "Synthesis of benzocarbazoles, indoloquinolines and indolonaphthridines from thermolysis of benzoenynyl ketenimines and carbodiimides." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2119.

Full text
Abstract:
Thesis (Ph. D.)--West Virginia University, 2001.
Title from document title page. Document formatted into pages; contains ix, 82 p. : ill. Includes abstract. Includes bibliographical references (p. 70-80).
APA, Harvard, Vancouver, ISO, and other styles
8

Krahl, Micha P. "Regioselektive Synthese oxygenierter Carbazole." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2007. http://nbn-resolving.de/urn:nbn:de:swb:14-1168004377329-87485.

Full text
Abstract:
In der heutigen Wirkstoffforschung stellen vor allem multiresistente Krankheitserreger eine große Herausforderung an die Wissenschaft dar. Noch sterben z.B. an der Tuberkulose jährlich etwa 1.7 Millionen Menschen, davon 69000 allein in Europa (WHO-Angaben, 2004). Die Tuberkulose verursacht neben AIDS die meisten Todesfälle unter den Infektionskrankheiten. Ein großes Problem sind die zahlreichen Neuerkrankungen, die mit herkömmlichen Mitteln nicht mehr behandelt werden können, sowie zunehmende Medikamentenallergien. Somit ist ein wichtiges Gebiet der Wirkstoff-forschung, neben der Weiterentwicklung bekannter Medikamente, deren Neuentwicklung. Dabei leistet die Natur eine unentbehrliche Orientierungshilfe. So konnte aus asiatischen Medizinalpflanzen in letzter Zeit eine Reihe von Carbazolalkaloiden isoliert werden, die zweifelsfrei gegen das HI-Virus oder das Mycobakterium tuberculose, dem Erreger der Tuberkulose, aktiv sind.[1] Ziel der vorliegenden Arbeit war die regioselektive Synthese oxygenierter Carbazole. Dabei wurde das Konzept der eisenvermittelten Carbazolsynthese angewendet und darüber hinaus als Alternative die palladiumvermittelte Carbazolsynthese weiterentwickelt. Die für den Palladiumweg benötigten N,N-Diarylamine konnten über die BUCHWALD-HARTWIG-Aminierung, die Eisensalzkomplexe über eine katalytische Komplexierung ausgehend von Cyclohexadienen mit Pentacarbonyleisen hergestellt werden. Beide Methoden wurden gegenübergestellt und besonders hinsichtlich ihrer Ausbeuten und Syntheseeffizienz verglichen.
APA, Harvard, Vancouver, ISO, and other styles
9

Krahl, Micha P. "Regioselektive Synthese oxygenierter Carbazole." Doctoral thesis, Technische Universität Dresden, 2006. https://tud.qucosa.de/id/qucosa%3A24953.

Full text
Abstract:
In der heutigen Wirkstoffforschung stellen vor allem multiresistente Krankheitserreger eine große Herausforderung an die Wissenschaft dar. Noch sterben z.B. an der Tuberkulose jährlich etwa 1.7 Millionen Menschen, davon 69000 allein in Europa (WHO-Angaben, 2004). Die Tuberkulose verursacht neben AIDS die meisten Todesfälle unter den Infektionskrankheiten. Ein großes Problem sind die zahlreichen Neuerkrankungen, die mit herkömmlichen Mitteln nicht mehr behandelt werden können, sowie zunehmende Medikamentenallergien. Somit ist ein wichtiges Gebiet der Wirkstoff-forschung, neben der Weiterentwicklung bekannter Medikamente, deren Neuentwicklung. Dabei leistet die Natur eine unentbehrliche Orientierungshilfe. So konnte aus asiatischen Medizinalpflanzen in letzter Zeit eine Reihe von Carbazolalkaloiden isoliert werden, die zweifelsfrei gegen das HI-Virus oder das Mycobakterium tuberculose, dem Erreger der Tuberkulose, aktiv sind.[1] Ziel der vorliegenden Arbeit war die regioselektive Synthese oxygenierter Carbazole. Dabei wurde das Konzept der eisenvermittelten Carbazolsynthese angewendet und darüber hinaus als Alternative die palladiumvermittelte Carbazolsynthese weiterentwickelt. Die für den Palladiumweg benötigten N,N-Diarylamine konnten über die BUCHWALD-HARTWIG-Aminierung, die Eisensalzkomplexe über eine katalytische Komplexierung ausgehend von Cyclohexadienen mit Pentacarbonyleisen hergestellt werden. Beide Methoden wurden gegenübergestellt und besonders hinsichtlich ihrer Ausbeuten und Syntheseeffizienz verglichen.
APA, Harvard, Vancouver, ISO, and other styles
10

Kirst, Juliane. "Synthese halogenierter Carbazole und Totalsynthese der Amaryllisalkaloide Pratosin und Hippadin." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-21142.

Full text
Abstract:
Während meiner Dissertation beschäftigte ich mich mit der Synthese von polyhalogenierten Carbazolderivaten. Das Carbazolgerüst wurde über den Palladiumvermittelten, bestehend aus Buchwald-Hartwig-Aminierung und oxidativer Cyclisierung, aufgebaut. Die Halogensubstituenten wurden entweder am Carbazol eingeführt oder bereits über die Startmoleküle in die Synthese eingebracht. Somit konnten verschiedene halogenierte halogenierte Derivate synthetisiert werden. Diese Verbindungen konnten in einer Kooperation mit Herrn Prof. Gutzeit aus der Fachrichtung Biologie der TU Dresden auf ihre Aktivität in der Inhibierung der Myosin ATPase untersucht werden. Dabei wurde ein tribromiertes 1-Hydroxycarbazol als wirksamer Inhibitor identifiziert. Der zweite Teil der Promotion umfasst die Darstellung der Amaryllisalkaloide Pratosin und Hippadin, sowie der auf diesem Weg ebenfalls zugänglichen Naturstoffe Assoanin, Oxoassoanin, Anhydrolycorin-7-on und deren Naturstoffanaloga Anhydrolycorin. Die Synthese wurde auf zwei verschiedenen Wegen durchgeführt und beinhaltet als Schlüsselreaktionen die Eisenvermittelte C-C und C-N Bindungsbildung, sowie die Palladiumvermittelte Biarylkupplung
This thesis is about my research study of the synthesis of polyhalogenated carbazoles. The skeletal structure of the carbazoles are easily assembled by palladium(0)-catalyzed Buchwald-Hartwig coupling and palladium(II)-mediated oxidative cyclisation. Through cooperation with Prof. Gutzeit many different halogenated carbazole derivatives could be analyzed concerning the activity of the inhibition of myosin ATPase. The tribrominated 1-Hydroxycarbazole was identified as sn effective inhibitor. The second part of my thesis includes the total synthesis of amaryllidaceae alkaloids pratosine, oxoassoanine, assoanine, hippadine, anhydrolycorinone and anhydrolycorine. The synthesis was accomplished by two different pathways which include the Iron-mediated C-C and C-N bond formation and intramolecular palladium-catalysed biaryl coupling reaction as the key steps
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Carbazole Alkaloids"

1

Bhattacharyya, P., and D. P. Chakraborty. "Carbazole Alkaloids." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, 159–209. Vienna: Springer Vienna, 1987. http://dx.doi.org/10.1007/978-3-7091-8906-1_4.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Chakraborty, D. P., and Shyamali Roy. "Carbazole Alkaloids III." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, 71–152. Vienna: Springer Vienna, 1991. http://dx.doi.org/10.1007/978-3-7091-9119-4_2.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Chakraborty, D. P., and Shyamali Roy. "Carbazole Alkaloids IV." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, 125–230. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6051-0_3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Bergman, Jan, and Benjamin Pelcman. "Synthetic Approaches to Carbazole Alkaloids." In Natural Products Chemistry III, 215–34. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-74017-6_11.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Bauer, Ingmar, and Hans-Joachim Knölker. "Synthesis of Pyrrole and Carbazole Alkaloids." In Topics in Current Chemistry, 203–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/128_2011_192.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Knölker, Hans-Joachim. "Occurrence, Biological Activity, and Convergent Organometallic Synthesis of Carbazole Alkaloids." In Topics in Current Chemistry, 115–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b96890.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Matsuoka, Junpei. "Construction of the Pyrrolo[2,3-d]Carbazole Core of Spiroindoline Alkaloids by Gold-Catalyzed Cascade Cyclization of Ynamide." In Total Synthesis of Indole Alkaloids, 67–79. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-8652-1_3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Knölker, Hans-Joachim, and Kethiri R. Reddy. "Biogenesis of Carbazole Alkaloids." In The Alkaloids: Chemistry and Biology, 159–80. Elsevier, 2008. http://dx.doi.org/10.1016/s1099-4831(07)00003-x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Knölker, Hans-Joachim, and Kethiri R. Reddy. "Chemistry of Carbazole Alkaloids." In The Alkaloids: Chemistry and Biology, 195–383. Elsevier, 2008. http://dx.doi.org/10.1016/s1099-4831(07)00005-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Knölker, Hans-Joachim, and Kethiri R. Reddy. "Biological and Pharmacological Activities of Carbazole Alkaloids." In The Alkaloids: Chemistry and Biology, 181–93. Elsevier, 2008. http://dx.doi.org/10.1016/s1099-4831(07)00004-1.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Carbazole Alkaloids"

1

Thant, Tin Myo, Nanik Siti Aminah, Alfinda Novi Kristanti, Rico Ramadhan, Hnin Thanda Aung, and Yoshiaki Takaya. "Cytotoxic Carbazole Alkaloid from the Root of Clausena cxcavata on Hela Cell Line." In International Conference on Chemical Science and Technology Innovation. SCITEPRESS - Science and Technology Publications, 2019. http://dx.doi.org/10.5220/0008858101410144.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Boonsnongcheep, P., S. Daodee, T. Kitisripanya, and W. Putalun. "Enhanced carbazole alkaloid and antioxidant capacity in callus culture of medicinal plant Clausena harmandiana by Bacilius subtilis elicitor." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399792.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Stadlbauer, Wolfgang, Daniel Rieder, Birgit Schuiki, and Thomas Kappe. "Syntheses, Substitution and Cyclization Reactions of 7a,8,9,10,11a-Hexahydro-pyrido[3,2,1-jk]carbazoles With a Strychnos Alkaloids Partial Structure." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a001.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Stadlbauer, Wolfgang, Ali Deeb, Urška Erklavec, Daniel Rieder, Birgit Schuiki, Fritz Stüber, and Thomas Kappe. "Syntheses and Reactions of 5-Unsubstituted 11b-Methyl-1,2,3,11b-tetrahydro-pyrido[3,2,1-jk]carbazoles Having a Strychnos Alkaloids Partial Structure." In The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a041.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Stadlbauer, Wolfgang, Ali Deeb, Urška Erklavec, Daniel Rieder, and Birgit Schuiki. "Syntheses and Reactions of 5-Alkyl- and 5-Aryl-11b-Methyl-1,2,3,11b-Tetrahydro-Pyrido[3,2,1-jk]carbazoles Having a Strychnos Alkaloids Partial Structure." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a005.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Carbazole Alkaloids' for particular source types:
Journal articles Dissertations / Theses
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography