Day: January 17, 2022

Authors Sviripa, VM; Fiandalo, MV; Begley, KL; Wyrebek, P; Kril, LM; Balia, AG; Parkin, SR; Subramanian, V; Chen, X; Williams, AH; Zhan, CG; Liu, CM; Mohler, JL; Watt, DS in ROYAL SOC CHEMISTRY published article about RESISTANT PROSTATE-CANCER; ANDROGEN RECEPTOR; DIHYDROTESTOSTERONE; TARGET; INHIBITORS; ANDROSTANEDIOL; DEHYDROGENASES; IDENTIFICATION; TESTOSTERONE; BIOCHEMISTRY in [Sviripa, Vitaliy M.; Williams, Alexander H.; Zhan, Chang-Guo] Univ Kentucky, Coll Pharm, Dept Pharmaceut Sci, Lexington, KY 40536 USA; [Sviripa, Vitaliy M.; Begley, Kristin L.; Wyrebek, Przemyslaw; Kril, Liliia M.; Balia, Andrii G.; Zhan, Chang-Guo; Watt, David S.] Univ Kentucky, Coll Pharm, Ctr Pharmaceut Res & Innovat, Lexington, KY 40536 USA; [Sviripa, Vitaliy M.; Liu, Chunming; Watt, David S.] Univ Kentucky, Lucille Parker Markey Canc Ctr, Lexington, KY 40536 USA; [Fiandalo, Michael, V; Mohler, James L.] Roswell Pk Comprehens Canc Ctr, Dept Expt Therapeut, Buffalo, NY 14263 USA; [Begley, Kristin L.; Wyrebek, Przemyslaw; Kril, Liliia M.; Balia, Andrii G.; Liu, Chunming; Watt, David S.] Univ Kentucky, Coll Med, Dept Mol & Cellular Biochem, Lexington, KY 40536 USA; [Parkin, Sean R.] Univ Kentucky, Coll Arts & Sci, Dept Chem, Lexington, KY 40506 USA; [Subramanian, Vivekanandan] Univ Kentucky, Coll Pharm, NMR Ctr, Lexington, KY 40536 USA; [Chen, Xi] South Cent Univ Nationalities, Coll Chem & Mat Sci, Wuhan 430074, Peoples R China; [Mohler, James L.] Roswell Pk Comprehens Canc Ctr, Dept Urol, Buffalo, NY 14263 USA in 2020.0, Cited 57.0. Computed Properties of C7H8O2. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6

Androgen-deprivation therapy (ADT) is only a palliative measure, and prostate cancer invariably recurs in a lethal, castration-resistant form (CRPC). Prostate cancer resists ADT by metabolizing weak, adrenal androgens to growth-promoting 5 alpha-dihydrotestosterone (DHT), the preferred ligand for the androgen receptor (AR). Developing small-molecule inhibitors for the final steps in androgen metabolic pathways that utilize 17-oxidoreductases required probes that possess fluorescent groups at C-3 and intact, naturally occurring functionality at C-17. Application of the Pictet-Spengler condensation to substituted 4-(2-aminoethyl)coumarins and 5 alpha-androstane-3-ones furnished spirocyclic, fluorescent androgens at the desired C-3 position. Condensations required the presence of activating C-7 amino orN,N-dialkylamino groups in the 4-(2-aminoethyl)coumarin component of these condensation reactions. Successful Pictet-Spengler condensation, for example, of DHT with 9-(2-aminoethyl)-2,3,6,7-tetrahydro-1H,5H,11H-pyrano[2,3-f]pyrido[3,2,1-ij]quinolin-11-one led to a spirocyclic androgen, (3R,5S,10S,13S,17S)-17-hydroxy-10,13-dimethyl-1,2,2 ‘,3 ‘,4,5,6,7,8,8 ‘,9,9 ‘,10,11,12,12 ‘,13,13 ‘,14,15,16,17-docosahydro-7 ‘ H,11 ‘ H-spiro-[cyclopenta[a]phenanthrene-3,4 ‘-pyrido[3,2,1-ij]pyrido[4 ‘,3 ‘:4,5]pyrano[2,3-f]quinolin]-5 ‘(1 ‘ H)-one. Computational modeling supported the surrogacy of the C-3 fluorescent DHT analog as a tool to study 17-oxidoreductases for intracrine, androgen metabolism.

Welcome to talk about 150-19-6, If you have any questions, you can contact Sviripa, VM; Fiandalo, MV; Begley, KL; Wyrebek, P; Kril, LM; Balia, AG; Parkin, SR; Subramanian, V; Chen, X; Williams, AH; Zhan, CG; Liu, CM; Mohler, JL; Watt, DS or send Email.. Computed Properties of C7H8O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

COA of Formula: C9H10O3. Authors Nayak, SS; Wadhawa, GC; Shivankar, VS; Patil, DD; Sonawale, MC; Mirgane, NA in ELSEVIER published article about in [Nayak, Shubhada S.; Wadhawa, Gurumeet C.] Karmaveer Bhaurao Patil Coll, Rayat Shikshan Sansthas, Vashi Sect 15 A Navi, Mumbai 400703, Maharashtra, India; [Shivankar, Vitthal S.] Chhatrapati Shivaji Coll, Rayat Shikshan Sansthas, Satara, Maharashtra, India; [Patil, Dinanath D.] SMBT Coll Sangamner, Sangamner 422605, MH, India; [Sonawale, Maryappa C.] Veer Wajekar ASC Coll, Raigad, MH, India; [Mirgane, Nitin A.] SIES Coll ASC, Dept Chem, Mumbai, Maharashtra, India in 2021.0, Cited 54.0. The Name is 3,4-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 120-14-9

The nanoscience is emerging field of the science and technology. In nanoscience research synthesizing green nanoparticles using green protocols are very good, effective technique, quite safe and ecofriendly technique compared to the conventional chemical and physical methods. These are used in the various field of science. These are used in the catalysis. Theses green and bio-based route for the preparation of the nanoparticles has good attention in the organic synthesis. These nano catalysts used for synthesis of heterocyclic compound. Imidazole and their derivatives are widely used. The imidazole and its derivatives are very important heterocyclic compounds. They have very good biological and pharmaceutical activity. In this we have prepared plant assisted tin oxide nanoparticles from the leaves of Ceropegia jainii plant by the green methods. The synthesized nanoparticles are characterized by various methods of analysis. These synthesized plants assisted nanoparticles are used for the synthesis of the heterocycles. We have developed the simple and highly efficient three component such as benzil, aromatic aldehyde and ammonium acetate under the microwave irradiation without any solvent. This reaction gives the 2,4,5-triarylimidazole derivatives with good yield and purity. This method is very simple and cost effective. Nano catalyst are green and recyclable with very less reaction time. (C) 2020 Elsevier Ltd. All rights reserved.

COA of Formula: C9H10O3. About 3,4-Dimethoxybenzaldehyde, If you have any questions, you can contact Nayak, SS; Wadhawa, GC; Shivankar, VS; Patil, DD; Sonawale, MC; Mirgane, NA or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Regioselective Ring-Opening of Glycidol to Monoalkyl Glyceryl Ethers Promoted by an [OSSO]-Fe-III Triflate Complex WOS:000476079000001 published article about VALUE-ADDED PRODUCT; 2,3-EPOXY ALCOHOLS; ORGANIC-SYNTHESIS; IRON CATALYSIS; CARBON-DIOXIDE; SUBSTRATE; EFFICIENT; EPOXIDES; METAL; TRANSFORMATION in [Della Monica, Francesco; Ricciardi, Maria; Proto, Antonio; Cucciniello, Raffaele; Capacchione, Carmine] Univ Salerno, Dipartimento Chim & Biol Adolfo Zambelli, Via Giovanni Paolo II, I-13284084 Salerno, SA, Italy in 2019.0, Cited 45.0. Formula: C7H8O. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6

A Fe-III-triflate complex, bearing a bis-thioether-di-phenolate [OSSO]-type ligand, was discovered to promote the ring-opening of glycidol with alcohols under mild reaction conditions (0.05 mol % catalyst and 80 degrees C). The reaction proceeded with high activity (initial turnover frequency of 1680 h(-1) for EtOH) and selectivity (>95 %) toward the formation of twelve monoalkyl glyceryl ethers (MAGEs) in a regioselective fashion (84-96 % yield of the non-symmetric regioisomer). This synthetic approach allows the conversion of a glycerol-derived platform molecule (i.e., glycidol) to high-value-added products by using an Earth-crust abundant metal-based catalyst.

About Benzyl Alcohol, If you have any questions, you can contact Della Monica, F; Ricciardi, M; Proto, A; Cucciniello, R; Capacchione, C or concate me.. Formula: C7H8O

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

I found the field of Chemistry very interesting. Saw the article Conversion of 3,6-O-Dimethylfluorescein to Fluorescein-Based Xanthylium Derivative: Characterization and Covalent Attachment to Bovine Serum Albumin published in 2019.0. COA of Formula: C7H8O2, Reprint Addresses Kalhor, HR (corresponding author), Sharif Univ Technol, Chem Dept, Biochem Res Lab, Tehran, Iran.. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol

Xanthene dyes, such as fluorescein and rhodamine, have played crucial rules in biological sciences especially covalent attachment of these organic compounds to biomolecules. 3-O-methylfluorescein and 3,6-O-dimethylfluorescein were synthesized and purified using a facile procedure. 3,6-O-dimethylfluorescein, which lacks fluorescence, was treated with sodium hydroxide and sulfuric acid solutions, giving rise to yellow and green fluorescent compounds, respectively. In both basic and acidic conditions, donor-acceptor structures were formed. The reaction of 3,6-O-dimethylfluorescein with acids, in a reversible manner, emitted green fluorescence, whereas its reaction with hydroxide ion, irreversibly shifted the fluorescence to the yellow region. Using MS spectrometry, the product identity was determined as a xanthylium ion derivative. Stokes shift and quantum yield for xanthylium ion were measured. Various nucleophiles were examined for studying the mechanism of the xanthylium ion in aqueous solutions; the results confirmed that hydroxide ion was mediatory for the emission of the fluorescence. In addition, 3-O-methyl-5(6)-carboxyfluorescein and 3,6-O-dimethyl-5(6)-carboxyfluorescein were synthesized that can potentially be used in bioorthogonal reactions for labeling proteins. The synthesized products were used in covalent attachment to bovine serum albumin (BSA) and their unique fluorescences were detected.

COA of Formula: C7H8O2. Bye, fridends, I hope you can learn more about C7H8O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recently I am researching about RING-DISTORTION; COMPLEX, Saw an article supported by the Swiss National Science FoundationSwiss National Science Foundation (SNSF)European Commission [P2SKP2_184064]; European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant [836947]; Max Planck SocietyMax Planck SocietyFoundation CELLEX; Projekt DEAL. Quality Control of 4-Methoxybenzaldehyde. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Liu, J; Cremosnik, GS; Otte, F; Pahl, A; Sievers, S; Strohmann, C; Waldmann, H. The CAS is 123-11-5. Through research, I have a further understanding and discovery of 4-Methoxybenzaldehyde

Natural product (NP) structures are a rich source of inspiration for the discovery of new biologically relevant chemical matter. In natural product inspired pseudo-NPs, NP-derived fragments are combined de novo in unprecedented arrangements. Described here is the design and synthesis of a 155-member pyrroquinoline pseudo-NP collection in which fragments characteristic of the tetrahydroquinoline and pyrrolidine NP classes are combined with eight different connectivities and regioisomeric arrangements. Cheminformatic analysis and biological evaluation of the compound collection by means of phenotyping in the morphological cell painting assay followed by principal component analysis revealed that the pseudo-NP classes are chemically diverse and that bioactivity patterns differ markedly, and are dependent on connectivity and regioisomeric arrangement of the fragments.

Quality Control of 4-Methoxybenzaldehyde. Welcome to talk about 123-11-5, If you have any questions, you can contact Liu, J; Cremosnik, GS; Otte, F; Pahl, A; Sievers, S; Strohmann, C; Waldmann, H or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

I found the field of Optics very interesting. Saw the article Design and synthesis of highly conjugated Electronic Phenanthrolines Derivatives for remarkable NLO properties and DFT analysis published in 2021. Recommanded Product: 123-11-5, Reprint Addresses Sahraoui, B (corresponding author), Univ Angers, Lab MOLTECH Anjou, CNRS, UMR 6200, 2 Bd Lavoisier, F-49045 Angers, France.; Bouchouit, K (corresponding author), Ville Univ, Ecole Normal Super Constantine, Constantine, Algeria.. The CAS is 123-11-5. Through research, I have a further understanding and discovery of 4-Methoxybenzaldehyde

The non-linear optical technology is gaining huge attention to the thermal and mechanical stability, electrical property, and modulate signal flexibility that could be used in uprising optoelectronics devices based on powerful laser technologies such as all optical switches, lightemitting diodes, data storage and optical communication systems. In this paper, selected three phenanthrolines derivatives [2-phenyl-1H-phenanthro[9,10-d]imidazole (1), 2-(4-nitrophenyl)1H-phenanthro[9,10-d]imidazole(2),2-(4-methoxyphenyl)-1H phenanthro[9,10-d]imidazole (3)] were synthesized and characterized using UV, FT-IR and H-1 NMR. Cubic nonlinear optical properties susceptibility (chi(<3>)(THG)) were analyzed and evaluated using the third harmonic generation technique on thin films at 1064 nm. The investigation study is completed by a theoretical calculation in which the different quantum chemical parameters like frontier molecular orbital analysis, energy gap, dipole moment, average polarizability, and first second hyperpolarizability were analyzed using Density Functional Theory (DFT). The non-linear optical behavior of the selected three phenanthrolines derivatives is confirmed through the obtained high THG efficiency. Moreover, a significant correlation between the molecular structures and the optoelectronic properties is demonstrated.

Recommanded Product: 123-11-5. Welcome to talk about 123-11-5, If you have any questions, you can contact Sahki, FA; Bouraiou, A; Taboukhat, S; Messaadia, L; Bouacida, S; Figa, V; Bouchouit, K; Sahraoui, B or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Application In Synthesis of 4-Methoxybenzaldehyde. Authors Rafferty, SM; Rutherford, JE; Zhang, LM; Wang, L; Nagib, DA in AMER CHEMICAL SOC published article about in [Rafferty, Sean M.; Rutherford, Joy E.; Zhang, Lumin; Wang, Lu; Nagib, David A.] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA in 2021.0, Cited 50.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

A cross-selective aza-pinacol coupling of aldehydes and imines has been developed to afford valuable beta-amino alcohols. This strategy enables chemoselective conversion of aliphatic aldehydes to ketyl radicals, in the presence of more easily reduced imines and other functional groups. Upon carbonyl-specific activation by AcI, a photoinitiated Mn catalyst selectively reduces the resulting alpha-oxy iodide by an atom transfer mechanism. The ensuing ketyl radical selectively couples to imines, precluding homodimerization by a classical reductive approach. In this first example of reductive, ketyl coupling by atom transfer catalysis, Zn serves as a terminal reductant to facilitate Mn catalyst turnover. This new strategy also enables ketyl radical couplings to alkenes, alkynes, aldehydes, propellanes, and chiral imines.

Welcome to talk about 123-11-5, If you have any questions, you can contact Rafferty, SM; Rutherford, JE; Zhang, LM; Wang, L; Nagib, DA or send Email.. Application In Synthesis of 4-Methoxybenzaldehyde

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

I found the field of Science & Technology – Other Topics very interesting. Saw the article Photoactivatable metabolic warheads enable precise and safe ablation of target cells in vivo published in 2021. Category: indole-building-block, Reprint Addresses Feng, Y; Vendrell, M (corresponding author), Univ Edinburgh, Queens Med Res Inst, Ctr Inflammat Res, Edinburgh, Midlothian, Scotland.. The CAS is 150-76-5. Through research, I have a further understanding and discovery of Mequinol

Metabolites can distinguish pathogenic from healthy cells, but they are hard to couple to current photosensitizers without altering their biological activity. Here the authors design a new family of photosensitizers that retain metabolite function to target pathogenic cells and ablate them by photodynamic therapy. Photoactivatable molecules enable ablation of malignant cells under the control of light, yet current agents can be ineffective at early stages of disease when target cells are similar to healthy surrounding tissues. In this work, we describe a chemical platform based on amino-substituted benzoselenadiazoles to build photoactivatable probes that mimic native metabolites as indicators of disease onset and progression. Through a series of synthetic derivatives, we have identified the key chemical groups in the benzoselenadiazole scaffold responsible for its photodynamic activity, and subsequently designed photosensitive metabolic warheads to target cells associated with various diseases, including bacterial infections and cancer. We demonstrate that versatile benzoselenadiazole metabolites can selectively kill pathogenic cells – but not healthy cells – with high precision after exposure to non-toxic visible light, reducing any potential side effects in vivo. This chemical platform provides powerful tools to exploit cellular metabolic signatures for safer therapeutic and surgical approaches.

Welcome to talk about 150-76-5, If you have any questions, you can contact Benson, S; de Moliner, F; Fernandez, A; Kuru, E; Asiimwe, NL; Lee, JS; Hamilton, L; Sieger, D; Bravo, IR; Elliot, AM; Feng, Y; Vendrell, M or send Email.. Category: indole-building-block

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Application In Synthesis of 4-Methoxybenzaldehyde. Authors Adler, C; Krivtsov, I; Mitoraj, D; dos Santos-Gomez, L; Garcia-Granda, S; Neumann, C; Kund, J; Kranz, C; Mizaikoff, B; Turchanin, A; Beranek, R in WILEY-V C H VERLAG GMBH published article about in [Adler, Christiane; Krivtsov, Igor; Mitoraj, Dariusz; Beranek, Radim] Ulm Univ, Inst Electrochem, Albert Einstein Allee 47, D-89081 Ulm, Germany; [dos Santos-Gomez, Lucia; Garcia-Granda, Santiago] Univ Oviedo, CINN, Dept Phys & Analyt Chem, Oviedo 33006, Spain; [Neumann, Christof; Turchanin, Andrey] Friedrich Schiller Univ Jena, Inst Phys Chem, Lessingstr 10, D-07743 Jena, Germany; [Neumann, Christof; Turchanin, Andrey] Friedrich Schiller Univ Jena, Abbe Ctr Photon, Lessingstr 10, D-07743 Jena, Germany; [Neumann, Christof; Turchanin, Andrey] Ctr Energy & Environm Chem Jena CEEC Jena, Philosophenweg 7a, D-07743 Jena, Germany; [Kund, Julian; Kranz, Christine; Mizaikoff, Boris] Ulm Univ, Inst Analyt & Bioanalyt Chem, Albert Einstein Allee 11, D-89081 Ulm, Germany in 2021, Cited 93. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

In spite of the enormous promise that polymeric carbon nitride (PCN) materials hold for various applications, the fabrication of high-quality, binder-free PCN films and electrodes has been a largely elusive goal to date. Here, we tackle this challenge by devising, for the first time, a water-based sol-gel approach that enables facile preparation of thin films based on poly(heptazine imide) (PHI), a polymer belonging to the PCN family. The sol-gel process capitalizes on the use of a water-soluble PHI precursor that allows formation of a non-covalent hydrogel. The hydrogel can be deposited on conductive substrates, resulting in formation of mechanically stable polymeric thin layers. The resulting photoanodes exhibit unprecedented photoelectrochemical (PEC) performance in alcohol reforming and highly selective (similar to 100 %) conversions with very high photocurrents (>0.25 mA cm(-2) under 2 sun) down to <0 V vs. RHE. This enables even effective PEC operation under zero-bias conditions and represents the very first example of a 'soft matter'-based PEC system capable of bias-free photoreforming. The robust binder-free films derived from sol-gel processing of water-soluble PCN thus constitute a new paradigm for high-performance 'soft matter' photoelectrocatalytic systems and pave the way for further applications in which high-quality PCN films are required. Welcome to talk about 123-11-5, If you have any questions, you can contact Adler, C; Krivtsov, I; Mitoraj, D; dos Santos-Gomez, L; Garcia-Granda, S; Neumann, C; Kund, J; Kranz, C; Mizaikoff, B; Turchanin, A; Beranek, R or send Email.. Application In Synthesis of 4-Methoxybenzaldehyde

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

I found the field of Chemistry very interesting. Saw the article Formation of furo[3,2-c]quinolone-2-carbonitriles and 4-oxo-4,5-dihydrofuro[3,2-c]quinolone-2-carboxamides from reaction of quinoline-2,4-diones with 2-[bis(methylthio)methylene]malononitrile published in 2020. Safety of 4-Hydroxyquinolin-2(1H)-one, Reprint Addresses Aly, AA (corresponding author), Menia Univ, Fac Sci, Chem Dept, El Minia 61519, Egypt.. The CAS is 86-95-3. Through research, I have a further understanding and discovery of 4-Hydroxyquinolin-2(1H)-one

Quinoline-2,4-diones reacted with 2-[bis(methylthio)methylene]malononitrile in DMF/Et3N to produce 3-(methylthio)-4-oxo-4,5-dihydrofuro[3,2-c]quinolone-2-carbonitriles and 3-(methylthio)-4-oxo-4,5-dihydrofuro[3,2-c]quinolone-2-carboxamides in state of 2-imino-substituted 4-(methylthio)-5,6-dihydro-2H-pyrano[3,2-c]quinolone-3-carbonitriles. The structures of all new products were proved using NMR, IR, and mass spectral data. The possible mechanism for the reaction is also discussed. Graphic abstract

Safety of 4-Hydroxyquinolin-2(1H)-one. Welcome to talk about 86-95-3, If you have any questions, you can contact Aly, AA; Ishak, E; Shwaky, AM; Mohamed, AH or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles