Month: October 2022

Sarkar, Souradip; Samanta, Rajarshi published the artcile< Weakly Coordinating tert-Amide-Assisted Ru(II)-Catalyzed Synthesis of Azacoumestans via Migratory Insertion of Quinoid Carbene: Application in the Total Synthesis of Isolamellarins>, HPLC of Formula: 23077-43-2, the main research area is azacoumestan preparation; diazonaphthoquinone indole migratory insertion cyclization ruthenium catalyst.

A weakly coordinating tert-amide-directed straightforward method was developed for the synthesis of azacoumestans, e.g., I, using the corresponding azaheterocycle derivatives II (R1 = H, Me, Bn, etc., R2 = H, Me, R3 = Cl, F, R4 = MeO, Br, Ph, etc.) and diazonaphthoquinones III (R5 = OH, R6 = Br, COMe, Ph, etc.) under cheap Ru(II)-catalyzed conditions. The reaction proceeds via migratory insertion of quinoid carbene and subsequent Bronsted acid-mediated cyclization. The optimized C2-selective method offered a wide scope of important azaheterocycles. Bioactive natural products like isolamellarins A and B were synthesized via the developed protocol. Preliminary mechanistic studies highlighted the probable mechanistic pathway.

Organic Letters published new progress about Alkaloids Role: SPN (Synthetic Preparation), PREP (Preparation) (isolamellarins). 23077-43-2 belongs to class indole-building-block, and the molecular formula is C9H6FNO2, HPLC of Formula: 23077-43-2.

Referemce:
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

Zhang, Ming-Zhi; Mulholland, Nick; Seville, Anne; Hough, Gemma; Smith, Nicholas; Dong, Hong-Qiang; Zhang, Wei-Hua; Gu, Yu-Cheng published the artcile< First discovery of pimprinine derivatives and analogs as novel potential herbicidal, insecticidal and nematicidal agents>, Application of C10H9NO, the main research area is pimprinine derivative analog preparation herbicidal insecticidal nematicidal.

Pimprinine and streptochlorin are indole natural products produced by many species of organisms, and they are reported to possess a wide range of biol. activities, such as anticancer, antiviral, antifungal activity and so on. In this study, three series of pimprinine derivatives or analogs were efficiently synthesized under the optimized methods. Biol. assays conducted at Syngenta firstly indicated the pimprinine derivatives or analogs possessed potential herbicidal and insecticidal activity, and this is highlighted by several compounds that possessed significant biol. activity as well as broad spectrum. Meanwhile, compounds with benzothiophene-oxazole core showed effective nematicidal activity in primary screening. Compounds 5-(benzofuran-3-yl)oxazole and 5-(benzodioxol-5-yl)oxazole were identified as the most promising lead structures for further study.

Tetrahedron published new progress about Disease, plant. 4771-48-6 belongs to class indole-building-block, and the molecular formula is C10H9NO, Application of C10H9NO.

Referemce:
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

Mumtaz, Yasir; Liu, Jie published the artcile< Iodine-catalyzed Regioselective Electrophilic (Fluoroalkyl) Sulfenylation of Indoles with (RSO2)2O via Deoxygenative Reduction>, Category: indole-building-block, the main research area is indole sulfonic anhydride iodine catalyst regioselective sulfenylation deoxygenative reduction; thioindole preparation.

A method for electrophilic C-H sulfenylation by deoxygenative reduction from less expensive and easily available sulfonic anhydrides was reported. This C-S bond-forming reaction allowed a general access to sulfenyl electrophiles, including important trifluoromethyl, perfluoroalkyl and aryl derivatives that are otherwise difficult to afford. Under metal-free conditions, the reaction yielded 3-arylthio (fluoroalkylthio) indoles in good to excellent yields. The catalytic technique tolerated a wide range of functional groups.

Asian Journal of Organic Chemistry published new progress about Indoles Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 93247-78-0 belongs to class indole-building-block, and the molecular formula is C10H9NO2, Category: indole-building-block.

Referemce:
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

Wang, Xiaochun; Li, Tiechun published the artcile< A novel ""off-on"" rhodamine-based colorimetric and fluorescent chemosensor based on hydrolysis driven by aqueous medium for the detection of Fe3+>, Related Products of 950846-89-6, the main research area is rhodamine colorimetric fluorescent chemosensor hydrolysis iron; Chemosensor; Fe(3+); Fluorescence enhancement; Living cell imaging; Rhodamine B.

A novel “”off-on”” colorimetric and fluorescent chemosensor N2,N6-bis(2-(rhodamine B amido)ethyl)pyridine-2,6-dicarboxamide (RhBEP) (I) has been designed and synthesized, which can selectively detect the presence of Fe3+ with about 75-fold enhancement in fluorescence emission intensity at 585 nm over various environmentally relevant metal cations such as Hg2+, Cu2+, Cr3+, Li+, Na+, K+, Ag+, Zn2+, Mg2+, Ca2+, Ba2+, Fe2+, Cd2+, Ni2+, Mn2+, Al3+, Bi3+ and Au3+ in PBS reaction media. The remarkable color change from UV-Vis titration experiments indicates that RhBEP can be used as a colorimetric chemosensor for Fe3+. The ultrasensitive detection limit for Fe3+ in the fluorescence measurement is down to 2.0 × 10-8 mol·L-1. The recognition mechanism of RhBEP to Fe3+ was analyzed by Job’s plot and mass spectrometry anal. In addition, the data from fluorescent cell imaging experiments confirmed that the chemosensor RhBEP has a promising application for the detection of Fe3+ in biol. systems.

Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy published new progress about Biological imaging. 950846-89-6 belongs to class indole-building-block, and the molecular formula is C30H36N4O2, Related Products of 950846-89-6.

Referemce:
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

Ji, Xiaoqian; Zhang, Wan; Ge, Fangqing; Wang, Chaoxia; Yin, Yunjie; Chen, Kunlin published the artcile< Thermochromic behavior analysis of terminated polyurethane functionalized with rhodamine B derivative>, Electric Literature of 950846-89-6, the main research area is rhodamine B derivative terminated polyurethane print thermochromic cotton fabric; thermochromic property.

A novel “”off-on”” terminated polyurethane based on the rhodamine B modified dye RhEA was constructed with the polyethylene glycol (PEG) and 1,4-butanediol (BDO) as soft segment, isophorone diisocyanate (IPDI) as hard segment. The RhEA terminated polyurethane turned to red from colorless after 254 nm UV induction accompanying transformation of RhEA from a twisted spirolactam to a planarized ring-opened amide. The intensity of absorbance enhanced as UV induction time increased. And the color of the RhEA terminated polyurethane changed from red turned to light red (45 °C) and colorless (65 °C), reversibly. The RhEA terminated polyurethane showed good thermal stability. The thermochromic cotton fabric was obtained with RhEA terminated polyurethane via flat screen printing and it turned to red from white after 254 nm UV induction. The K/S values decreased nearly 65.8% at 45 °C compared to 40 °C suggesting the thermochromic cotton became light red and it turned to white completely at 65 °C. The lactam ring was still retained during the printing process and the thermochromic cotton fabric possessed thermochromic behavior after UV induction. They can be a promising candidate for developing a flexible sensor to monitor environmental changes.

Progress in Organic Coatings published new progress about Color. 950846-89-6 belongs to class indole-building-block, and the molecular formula is C30H36N4O2, Electric Literature of 950846-89-6.

Referemce:
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

Zhang, Yan; Hu, Zhe-Yao; Li, Xin-Chang; Guo, Xun-Xiang published the artcile< Copper-Catalyzed Decarboxylative N-Arylation of Indole-2-Carboxylic Acids>, Name: 5-Fluoroindole-2-carboxylic acid, the main research area is aryl indole preparation; indole carboxylic acid aryl halide copper catalyst decarboxylative arylation.

A novel decarboxylative N-arylation of indole-2-carboxylic acids with aryl halides was developed. The reaction proceeded efficiently in the presence of Cu2O as the catalyst to give the corresponding N-aryl indoles I [R1 = 4-Me, 5-F, 6-MeO, etc.; R2 = Ph, 3-FC6H4, 4-ClC6H4, etc.] in high yields. This synthetic method showed good functional group tolerance and offered an alternative route to construct N-aryl indoles.

Synthesis published new progress about Aryl bromides Role: RCT (Reactant), RACT (Reactant or Reagent). 399-76-8 belongs to class indole-building-block, and the molecular formula is C9H6FNO2, Name: 5-Fluoroindole-2-carboxylic acid.

Referemce:
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

Wang, Lei; Zhou, Ying; Zhang, Yan; Zhang, Guomei; Zhang, Caihong; He, Yujian; Dong, Chuan; Shuang, Shaomin published the artcile< A novel cell-penetrating Janus nanoprobe for ratiometric fluorescence detection of pH in living cells>, SDS of cas: 950846-89-6, the main research area is cell penetrating Janus nanoprobe ratiometry fluorescence pH cell imaging; Intracelluar pH; Janus nanoprobe; Ratiometric detection.

pH regulates the function of many organelles and plays a pivotal role in requiring multitud cellular behaviors. Compared with single fluorescent probes, ratio fluorescent probes have higher sensitivity and immunity to interference. Herein, a novel Janus ratio nanoprobe was developed for intracellular pH detection. Modified rhodamine B probe and fluorescein isothiocyanate (FITC) were individually encapsulated in the independent hemispheres of Janus microparticles fabricated via Pickering emulsion. Moreover, it exhibits a satasified ratiometric detection of pH compared to the previous core-shell structure and organic small mol. probe. Accordingly, the Janus nanoprobe possesses many important features as an attractive sensor, including high anti-jamming capability, excellent stability, good reversibility and low cytotoxicity. Variations of the two fluorescence intensities (Fgreen/Fred) resulted in a ratiometric pH fluorescent sensor, which can respond to wide range of pH values from 3 to 8. To be more specific, with a single excitation wavelength of 488 nm, there are dual emission bands centered at 538 nm and 590 nm. Also the Janus nanoprobe displays a excellent linear relation in the physiol. relevant pH range of 4.0-6.0. Consequently, detecting of pH and imaging was successfully achieved in living cells, which provides a simple and reliable method for detecting intracelluar pH and other similar substances.

Talanta published new progress about Acid-base indicators. 950846-89-6 belongs to class indole-building-block, and the molecular formula is C30H36N4O2, SDS of cas: 950846-89-6.

Referemce:
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

Zhang, Ming-Zhi; Chen, Qiong; Xie, Cai-Hong; Mulholland, Nick; Turner, Sarah; Irwin, Dianne; Gu, Yu-Cheng; Yang, Guang-Fu; Clough, John published the artcile< Synthesis and antifungal activity of novel streptochlorin analogues>, Application In Synthesis of 4771-48-6, the main research area is streptochlorin analog preparation antifungal; Antifungal activity; Natural product; Streptochlorin; Structure–activity relationships; Synthesis.

Streptochlorin, first isolated as a new antibiotic in 1988 from the lipophilic extracts of the mycelium of a Streptomyces sp., is an indole natural product with a variety of biol. activities. Based on the methods developed for the synthesis of pimprinine in our laboratory, we have synthesized a series of indole-modified streptochlorin analogs and measured their activities against seven phytopathogenic fungi. Some of the analogs displayed good activity in the primary assays, and seven compounds were identified as the most promising candidates for further study. Structural optimization is still ongoing with the aim of discovering synthetic analogs with improved antifungal activity.

European Journal of Medicinal Chemistry published new progress about Fungicides. 4771-48-6 belongs to class indole-building-block, and the molecular formula is C10H9NO, Application In Synthesis of 4771-48-6.

Referemce:
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

Lai, Yi-Huan; Wu, Run-Shi; Huang, Jie; Huang, Jun-Yu; Xu, Da-Zhen published the artcile< Iron-Catalyzed Oxidative Coupling of Indoline-2-ones with Aminobenzamides via Dual C-H Functionalization>, Quality Control of 20870-77-3, the main research area is oxindole aminobenzamide iron catalyst oxidative coupling reaction; spioroindolinequinazoline dione preparation.

We describe an unprecedented dual C-H functionalization of indolin-2-one via an oxidative C(sp3)-H/N-H/X-H (X = N, C, S) cross-coupling protocol, which was catalyzed by a simple iron salt under mild and ligand-free conditions and employs air (mol. oxygen) as the terminal oxidant. This method was readily applicable for the construction of tetrasubstituted carbon centers from methylenes and provides a wide variety of spiro N-heterocyclic oxindoles.

Organic Letters published new progress about Amino amides Role: RCT (Reactant), RACT (Reactant or Reagent). 20870-77-3 belongs to class indole-building-block, and the molecular formula is C8H6ClNO, Quality Control of 20870-77-3.

Referemce:
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

Tian, Xing-Ling; Feng, Chao; Zhao, Xu-Hui published the artcile< Corrosion Monitoring Effect of Rhodamine-Ethylenediamine on Copper Relics under a Protective Coating>, Application of C30H36N4O2, the main research area is rhodamine ethylenediamine copper relics protective coating corrosion.

Fluorescence spectroscopy is a common technique used to monitor early metallic corrosion. The fluorescence response characteristics of rhodamine-ethylenediamine toward Cu2+ have been studied using fluorescence and IR spectroscopy. Fluorescence microscopy and electrochem. impedance spectroscopy were used to study the monitoring effect of rhodamine-ethylenediamine on the corrosion of copper relics protected by an epoxy coating. The results showed a strong fluorescent response and selectivity toward Cu2+ that existed using rhodamine-ethylenediamine. Early metallic corrosion of copper relics can be effectively monitored upon adding 0.8 wt% rhodamine-ethylenediamine to an epoxy coating. When the soaking time was increased, the fluorescence intensity of the fluorescent area on the coating became stronger. In addition, the area of the luminous coating reached ∼0.06 mm2 and the area of corrosion under the protective coating was ∼0.008 mm2, which was about 1/10 of the fluorescence area observed on the coating.

ACS Omega published new progress about Coating process. 950846-89-6 belongs to class indole-building-block, and the molecular formula is C30H36N4O2, Application of C30H36N4O2.

Referemce:
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