Category: 123-11-5

Recently I am researching about ONE-POT SYNTHESIS; CUFE2O4 NANOPARTICLES; EFFICIENT SYNTHESIS; TYROSINE KINASE; DERIVATIVES; GREEN; INHIBITOR; PARTICLES; AGENTS; ACIDS, Saw an article supported by the Science and Engineering Research Board; DST-INSPIRE fellowship [IF170498]; Council of Scientific and Industrial Research (CSIR), IndiaCouncil of Scientific & Industrial Research (CSIR) – India [02(0280)/16/EMRII]; Department of Science and Technology-Science and Engineering Research Board, India [EMR/2016/003126]. Published in WILEY in HOBOKEN ,Authors: Bhuyan, AJ; Bhuyan, P; Boruah, B; Saikia, L. The CAS is 123-11-5. Through research, I have a further understanding and discovery of 4-Methoxybenzaldehyde. Formula: C8H8O2

In recent years, magnetically active CuFe2O4 nanoparticles have been gaining significant interest in the field of heterogeneous catalysis as those can be easily prepared and effortlessly recovered from a reaction system. Here, we are reporting our work on cascade syntheses of 1,3-dimethyl-6-nitro-5-arylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-diones starting from 6-[(dimethylamino)methylene-amino]-1,3-dimethyluracil, aromatic aldehydes and nitromethane using magnetically active CuFe2O4 catalyst system under microwave irradiation and solvent-less condition. The current methodology is a valued addition to the existing procedures of 5-arylpyrido[2,3-d]pyrimidines syntheses making best use of the diene behavior of 6-[(dimethylamino)methylene-amino]-1,3-dimethyluracil. However, heterogeneous catalysis has been employed for the first time to do the syntheses by carrying out [4 + 2]cycloaddition reaction between 6-[(dimethylamino)methylene-amino]-1,3-dimethyluracil and in situ generated 2-(2-nitrovinyl)arenes/heteroarenes. The methodology is highly time-economic, and along with other features like easy recovery and good reusability of the catalyst, simple operating procedure, wide substrate scope, and good to excellent product yield, it offers the chemists a reaction protocol worth trying for the syntheses of 1,3-dimethyl-6-nitro-5-arylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-diones. While laboratory prepared catalyst system was characterized using FT-IR, XRD, SEM-EDX, VSM, XPS and TEM analysis, all the synthesized compounds have been characterized using H-1 and C-13 NMR spectroscopy and HRMS.

Bye, fridends, I hope you can learn more about C8H8O2, If you have any questions, you can browse other blog as well. See you lster.. Formula: C8H8O2

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

Authors Mourad, AAE; Khodir, AE; Saber, S; Mourad, MAE in MDPI published article about in [Mourad, Ahmed A. E.] Port Said Univ, Fac Pharm, Pharmacol & Toxicol Dept, Port Said 42511, Egypt; [Khodir, Ahmed E.] Horus Univ, Fac Pharm, Pharmacol Dept, New Damietta 34518, Egypt; [Saber, Sameh] Delta Univ Sci & Technol, Fac Pharm, Pharmacol Dept, Mansoura 11152, Dakahlia, Egypt; [Mourad, Mai A. E.] Port Said Univ, Fac Pharm, Med Chem Dept, Port Said 42511, Egypt in 2021, Cited 55. HPLC of Formula: C8H8O2. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Background: Dipeptidyl peptidase-4 (DPP-4) inhibitors have emerged as anti-hyperglycemic agents that improve glycemic control in type 2 diabetic patients, either as monotherapy or in combination with other antidiabetic drugs. Methods: A novel series of dihydropyrimidine phthalimide hybrids was synthesized and evaluated for their in vitro and in vivo DPP-4 inhibition activity and selectivity using alogliptin as reference. Oral glucose tolerance test was assessed in type 2 diabetic rats after chronic treatment with the synthesized hybrids +/- metformin. Cytotoxicity and antioxidant assays were performed. Additionally, molecular docking study with DPP-4 and structure activity relationship of the novel hybrids were also studied. Results: Among the synthesized hybrids, 10g, 10i, 10e, 10d and 10b had stronger in vitro DPP-4 inhibitory activity than alogliptin. Moreover, an in vivo DPP-4 inhibition assay revealed that 10g and 10i have the strongest and the most extended blood DPP-4 inhibitory activity compared to alogliptin. In type 2 diabetic rats, hybrids 10g, 10i and 10e exhibited better glycemic control than alogliptin, an effect that further supported by metformin combination. Finally, 10j, 10e, 10h and 10d had the highest radical scavenging activity in DPPH assay. Conclusions: Hybrids 10g, 10i and 10e are potent DPP-4 inhibitors which may be beneficial for T2DM treatment.

HPLC of Formula: C8H8O2. Welcome to talk about 123-11-5, If you have any questions, you can contact Mourad, AAE; Khodir, AE; Saber, S; Mourad, MAE 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

Recommanded Product: 123-11-5. Authors Rai, P; Chettri, P; Kar, S; Nagar, MA; Srivastava, S; Golakoti, NR in SPRINGER INTERNATIONAL PUBLISHING AG published article about in [Rai, Prashant; Kar, Swayamsiddha; Golakoti, Nageswara Rao] Sri Sathya Sai Inst Higher Learning, Dept Chem, Prasanthinilayam 515134, Andhra Pradesh, India; [Chettri, Prajal; Nagar, Malhar Anupam; Srivastava, Shailesh] Sri Sathya Sai Inst Higher Learning, Dept Phys, Prasanthinilayam 515134, Andhra Pradesh, India in 2021, Cited 35. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Fifteen chalcone derivatives having D-A-D, D-A-A and A-A-D architectures have been synthesized by Claisen-Schmidt condensation reaction and characterized by UV-Vis, IR, H-1-NMR, C-13-NMR and Mass spectrometry. In order to unambiguously establish the structure-activity relationship for the non-linear optical activity of these compounds, for the first time to our knowledge, we use the femtosecond degenerate four wave mixing (DFWM) technique to quantify and compare the third-order non-linear optical (NLO) activity of all the 15 compounds, under identical conditions. The second harmonics generation (SHG) efficiencies for all the compounds have also been evaluated using the Kurtz-Perry powder method. Among the compounds that we have synthesized here, the ones with A-A-D architecture show the highest NLO activity. Our results show that the NLO activity of a compound with A-A-D architecture can be further enhanced by incorporating a substituent with strong electron withdrawing ability on ring A and strong electron donating substituent on ring B. The results of the in silico studies that we have carried out correlate well with our experimental findings. The compounds (E)-3-(4-(dimethylamino)phenyl)-1-(4-nitrophenyl)prop-2-en-1-one with the compound code (4-N(CH3)(2)-4 ‘-NO2) and (E)-3-(4-methoxyphenyl)-1-(4-nitrophenyl)prop-2-en-1-one with the compound code (4-MeO-4 ‘-NO2) show the highest NLO activity among the compounds we have reported here.

Recommanded Product: 123-11-5. Bye, fridends, I hope you can learn more about C8H8O2, 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

Name: 4-Methoxybenzaldehyde. Xiao, WR; Li, SJ; Zhao, Y; Ma, YB; Li, N; Zhang, J; Chen, XN in [Xiao, Wanru; Li, Shujun; Zhao, Yue; Ma, Yubin; Li, Na; Zhang, Jie; Chen, Xuenian] Henan Normal Univ, Sch Chem & Chem Engn, Henan Key Lab Boron Chem & Adv Energy Mat,Key Lab, Minist Educ,Collaborat Innovat Ctr Henan Prov Gre, Xinxiang 453007, Henan, Peoples R China; [Chen, Xuenian] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450001, Peoples R China published Multinuclear transition metal-containing polyoxometalates constructed from Nb/W mixed-addendum precursors: synthesis, structures and catalytic performance in 2021.0, Cited 41.0. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

Four new transition metal-containing Nb/W mixed-addendum POM trimers with the formula H-19[M-4(H2O)(x)(P2W15Nb3O62)(3)]center dot m(HCOOH)center dot nH(2)O (M = Cu, x = 15, m = 0, and n = 21, Cu-POM; M = Co, x = 7, m = 0, and n = 15, Co-POM; M = Mn, x = 7, m = 6, and n = 18, Mn-POM; and M = Zn, x = 7, m = 0, and n = 23, Zn-POM) have been synthesized by a solvothermal method in a water-ethanol mixed solvent. All the four compounds were characterized by single-crystal X-ray diffraction, powder X-ray diffraction (XRD), IR spectroscopy, thermogravimetric analysis (TGA), and X-ray photoelectron spectroscopy (XPS). These compounds can serve as efficient heterogeneous catalysts for the cyanosilylation of different carbonyl compounds under ambient temperature and solvent-free conditions, and Cu-POM shows much better catalytic performance than the other three compounds. The cycle experiment showed that Cu-POM can be reused for at least five cycles without significant loss of catalytic activity. The IR spectroscopy and XRD analysis revealed that Cu-POM can retain its integrity after catalysis.

Welcome to talk about 123-11-5, If you have any questions, you can contact Xiao, WR; Li, SJ; Zhao, Y; Ma, YB; Li, N; Zhang, J; Chen, XN or send Email.. Name: 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

Category: indole-building-block. Authors Simeonova, R; Zheleva, D; Valkova, I; Stavrakov, G; Philipova, I; Atanasova, M; Doytchinova, I in MDPI published article about in [Simeonova, Rumyana; Zheleva, Dimitrina; Valkova, Iva; Stavrakov, Georgi; Atanasova, Mariyana; Doytchinova, Irini] Med Univ Sofia, Fac Pharm, Sofia 1000, Bulgaria; [Stavrakov, Georgi; Philipova, Irena] Bulgarian Acad Sci, Inst Organ Chem, Ctr Phytochem, Sofia 1113, Bulgaria in 2021, Cited 61. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

The acetylcholinesterase (AChE) inhibitors are the main drugs for symptomatic treatment of neurodegenerative disorders like Alzheimer’s disease. A recently designed, synthesized and tested hybrid compound between the AChE inhibitor galantamine (GAL) and the antioxidant polyphenol curcumin (CU) showed high AChE inhibition in vitro. Here, we describe tests for acute and short-term toxicity in mice as well as antioxidant tests on brain homogenates measured the levels of malondialdehide (MDA) and glutathione (GSH) and in vitro DPPH, ABTS, FRAP and LPO inhibition assays. Hematological and serum biochemical analyses were also performed. In the acute toxicity tests, the novel AChE inhibitor given orally in mice showed LD50 of 49 mg/kg. The short-term administration of 2.5 and 5 mg/kg did not show toxicity. In the ex vivo tests, the GAL-CU hybrid performed better than GAL and CU themselves; in a dose of 5 mg/kg, it demonstrates 25% reduction in AChE activity, as well as a 28% and 73% increase in the levels of MDA and GSH, respectively. No significant changes in blood biochemical data were observed. The antioxidant activity of 4b measured ex vivo was proven in the in vitro tests. In the ABTS assay, 4b showed radical scavenging activity 10 times higher than the positive control butylhydroxy toluol (BHT). The GAL-CU hybrid is a novel non-toxic AChE inhibitor with high antioxidant activity which makes it a prospective multitarget drug candidate for treatment of neurodegenerative disorders.

Welcome to talk about 123-11-5, If you have any questions, you can contact Simeonova, R; Zheleva, D; Valkova, I; Stavrakov, G; Philipova, I; Atanasova, M; Doytchinova, I 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

Authors Abu-Hashem, AA; Al-Hussain, SA; Zaki, MEA in MDPI published article about in [Abu-Hashem, Ameen Ali; Zaki, Magdi E. A.] Natl Res Ctr, Photochem Dept, Heterocycl Unit, Giza 12622, Egypt; [Abu-Hashem, Ameen Ali] Jazan Univ, Chem Dept, Fac Sci, Jazan 45142, Saudi Arabia; [Al-Hussain, Sami A.; Zaki, Magdi E. A.] Imam Mohammad Ibn Saud Islamic Univ IMSIU, Dept Chem, Fac Sci, Riyadh 13318, Saudi Arabia in 2021.0, Cited 50.0. Application In Synthesis of 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

In this article, we showed the synthesis of new polycyclic aromatic compounds, such as thienotriazolopyrimidinones, N-(thienotriazolopyrimidine) acetamide, 2-mercapto-thienotriazolo-pyrimidinones, 2-(((thieno-triazolopyrimidine) methyl) thio) thieno-triazolopyrimidines, thieno-pyrimidotriazolo-thiazines, pyrrolo-triazolo-thienopyrimidines, thienopyrimido-triazolopyrrolo-quinoxalines, thienopyrimido-triazolo-pyrrolo-oxathiino-quinoxalinones, 1,4-oxathiino-pyrrolo- triazolothienopyrimidinones, imidazopyrrolotriazolothienopyrimidines and 1,2,4-triazoloimidazo- pyrrolotriazolothienopyrimidindiones, based on the starting material 2,3-diamino-6-benzoyl-5- methylthieno[2,3-d]pyrimidin-4(3H)-one (3). The chemical structures were confirmed using many spectroscopic ways (IR, H-1, C-13, -NMR and MS) and elemental analyses. A series of thiazine, imidazole, pyrrole, thienotriazolopyrimidine derivatives were synthesized and evaluated for their antiproliferative activity against four human cancer cell lines, i.e., CNE2 (nasopharyngeal), KB (oral), MCF-7 (breast) and MGC-803 (gastric) carcinoma cells. The compounds 20, 19, 17, 16 and 11 showed significant cytotoxicity against types of human cancer cell lines.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Abu-Hashem, AA; Al-Hussain, SA; Zaki, MEA or concate me.. 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

Recently I am researching about ATOMIC-ABSORPTION-SPECTROMETRY; TETRACHLOROSILANE; REAGENT, Saw an article supported by the . Published in ELSEVIER SCIENCE SA in LAUSANNE ,Authors: Abdelghany, AM; Soliman, HA; Khatab, TK. The CAS is 123-11-5. Through research, I have a further understanding and discovery of 4-Methoxybenzaldehyde. Name: 4-Methoxybenzaldehyde

In recent years, a lot of benefits of Selenium have been discovered for humans, animals and chemical uses. Nano-Selenium was biosynthesized and characterized by using FTIR, UV/Vis., TEM/SAED, and mapping to ensure their crystallinity. The N-bridged imidazo-quinazoline derivatives were successfully synthesized in pentacyclic nonlinear ortho fused polynuclear by a one-pot reaction of aldehyde, beta-naphthol, and 2-aminobenzoimidazole in the presence of a catalytic amount of aqueous nano-Se as a highly efficient and facile catalyst at 70-80 degrees C. The molecular docking study as TRPV1 inhibitor compared with Rutaecarpine and Evodiamine as reference alkaloids ligands. (C) 2021 Elsevier B.V. All rights reserved.

Name: 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Abdelghany, AM; Soliman, HA; Khatab, TK 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

Authors Xi, ZW; Yang, L; Wang, DY; Feng, CW; Qin, YF; Shen, YM; Pu, CD; Peng, XG in AMER CHEMICAL SOC published article about in [Xi, Zi-Wei; Wang, Dan-Yan; Feng, Chuan-Wei; Shen, Yong-Miao] Zhejiang Sci Tech Univ, Dept Chem, Key Lab Surface & Interface Sci Polymer Mat Zheji, Hangzhou 310018, Zhejiang, Peoples R China; [Yang, Lei; Peng, Xiaogang] Zhejiang Univ, Ctr Chem Novel & High Performance Mat, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China; [Qin, Yufeng; Pu, Chaodan] Shanghai Tech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China in 2021.0, Cited 133.0. Safety of 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

We present an efficient and versatile visible light-driven methodology to transform aryl aldehydes and ketones chemoselectively either to alcohols or to pinacol products with CdSe/CdS core/shell quantum dots as photocatalysts. Thiophenols were used as proton and hydrogen atom donors and as hole traps for the excited quantum dots (QDs) in these reactions. The two products can be switched from one to the other simply by changing the amount of thiophenol in the reaction system. The core/shell QD catalysts are highly efficient with a turn over number (TON) larger than 4 X 10(4) and 4 X 10(5) for the reduction to alcohol and pinacol formation, respectively, and are very stable so that they can be recycled for at least 10 times in the reactions without significant loss of catalytic activity. The additional advantages of this method include good functional group tolerance, mild reaction conditions, the allowance of selectively reducing aldehydes in the presence of ketones, and easiness for large scale reactions. Reaction mechanisms were studied by quenching experiments and a radical capture experiment, and the reasons for the switchover of the reaction pathways upon the change of reaction conditions are provided.

Bye, fridends, I hope you can learn more about C8H8O2, If you have any questions, you can browse other blog as well. See you lster.. Safety 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

In 2021 BIOORG CHEM published article about HETEROCYCLIC RING-SYSTEMS; TUMOR-NECROSIS-FACTOR; BIOLOGICAL EVALUATION; INFLAMMATION; CARRAGEENAN; ANALOGS; COX-2 in [Abd El-Karim, Somaia S.; Mohamed, Hanaa S.] Natl Res Ctr, Dept Therapeut Chem, Cairo 12622, Egypt; [Abdelhameed, Mohamed F.] Natl Res Ctr, Pharmacol Dept, Cairo 12622, Egypt; [Amr, Abd El-Galil E.; Almehizia, Abdulrahman A.] King Saud Univ, Coll Pharm, Pharmaceut Chem Dept, Drug Explorat & Dev Chair DEDC, Riyadh 11451, Saudi Arabia; [Amr, Abd El-Galil E.] Natl Res Ctr, Appl Organ Chem Dept, Cairo 12622, Egypt; [Nossier, Eman S.] Al Azhar Univ, Fac Pharm Girls, Pharmaceut Med Chem Dept, Cairo, Egypt in 2021, Cited 41. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Safety of 4-Methoxybenzaldehyde

A new set of derivatives bearing pyrazole-methylenehydrazono-thiazolidinone scaffold 4-23 was designed, synthesized and confirmed by different spectroscopic means and elemental analyses. In-vivo anti-inflammatory and ulcerogenic evaluation was performed for all the newly synthesized derivatives using indomethacin, celecoxib and diclofenac as standard drugs. The compounds 5, 10, 15, 17, 21, 22 appeared to be the most promising candidates producing rapid onset and long duration of anti-inflammatory activity as well as promising GIT safety profile. Furthermore, analgesic evaluation revealed that the compounds 5, 10, 15 and 22 produced potent and long acting analgesia accompanied with significant inhibition of the inflammatory cytokine TNF-alpha level in comparison with the standard drugs. Molecular docking study of the latter derivatives was also carried out to rationalize their binding affinities and their modes of interactions with the active site of TNF-alpha.

Welcome to talk about 123-11-5, If you have any questions, you can contact Abd El-Karim, SS; Mohamed, HS; Abdelhameed, MF; Amr, AE; Almehizia, AA; Nossier, ES or send Email.. Safety 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

Authors Indurthi, HK; Virdi, R; Koli, P; Rao, DN; Sharma, DK in TAYLOR & FRANCIS INC published article about FRIEDEL-CRAFTS ALKYLATION; EFFICIENT; 3,3′-DIINDOLYLMETHANE; ALDEHYDES; ACID; DERIVATIVES; INDOLYLMETHANES; ALKALOIDS; BACTERIUM; ACCESS in [Indurthi, Harish K.; Koli, Papita; Sharma, Deepak K.] Banaras Hindu Univ, Dept Pharmaceut Engn & Technol, Indian Inst Technol, Varanasi 221005, Uttar Pradesh, India; [Virdi, Reena] Overseas Healthcare Pvt Ltd, Phillaur, India; [Nageswara Rao, Desaboini] Univ Massachusetts, Sch Med, Dept Biochem & Mol Pharmacol, Worcester, MA 01655 USA in 2021, Cited 70. HPLC of Formula: C8H8O2. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

A highly inexpensive, and operationally simple seralite SRC-120 (strongly acidic cation exchange resin) catalyzed synthesis of 3,3 ‘-bis(indolyl)methanes (BIMs) from indoles and low/high boiling point carbonyl compounds under solvent-free condition is reported. Synthesis of BIMs with low boiling point carbonyls at room temperature takes prolonged reaction time and give low yields at high temperature. The reported method overcomes these limitations and works remarkably well with low/high boiling point aldehydes/ketones in shorter reaction times (5-10 min) under microwave irradiation conditions and provides moderate to excellent yields (65-94%). Moreover, the recyclability of the catalyst for at least five times without notable loss in activity makes the whole process attractive and green protocol.

Welcome to talk about 123-11-5, If you have any questions, you can contact Indurthi, HK; Virdi, R; Koli, P; Rao, DN; Sharma, DK or send Email.. HPLC of Formula: C8H8O2

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