Category: 99-93-4

SDS of cas: 99-93-4. Yang, S; Xiong, MF; Tian, WQ; Zhang, H; Xiao, XY; Liu, HY; Chang, CK in [Yang, Shuang; Xiong, Ming-Feng; Tian, Wan-Qun; Zhang, Hao; Xiao, Xin-Yan; Liu, Hai-Yang] South China Univ Technol, Dept Chem, Key Lab Funct Mol Engn Guangdong Prov, Guangzhou 510641, Peoples R China; [Chang, Chi-Kwong] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA published Construction of C-O bond via cross-dehydrogenative coupling of sp [3] C-H bond with phenols catalyzed by copper porphyrin in 2020, Cited 42. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

Copper porphyrin-catalyzed construction of ether bond by cross-dehydrogenative coupling of sp [3] C-H bond with phenols bearing electron-withdrawing groups (EWG) was described for the first time. A broad range of substrates afforded different acetals in moderate to excellent yields with good functional group tolerance. The developed method is not only suitable for phenol substrates with ortho-directing groups, but also suitable for those phenol without ortho-directing groups. Significantly, a high turnover number (TON) up to 7300 was achieved in gram-level test. (C) 2020 Elsevier Ltd. All rights reserved.

Welcome to talk about 99-93-4, If you have any questions, you can contact Yang, S; Xiong, MF; Tian, WQ; Zhang, H; Xiao, XY; Liu, HY; Chang, CK or send Email.. SDS of cas: 99-93-4

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 Chao, CL; Huang, HC; Ding, HY; Lai, JH; Lin, HC; Chang, WL in TAYLOR & FRANCIS LTD published article about FANG-FENG-CAO; ANISOMELES-INDICA; AERIAL PARTS; GLYCOSIDES; OVATODIOLIDE; CONSTITUENTS; GLUCOSIDES; PHENOLS; CELLS in [Chao, Chen-Liang; Lin, Hang-Ching] Sinphar Pharm Co Ltd, Res & Dev Ctr, Ilan, Taiwan; [Huang, Hui-Chi] China Med Univ, Dept Chinese Pharmaceut Sci & Chinese Med Resourc, Taichung, Taiwan; [Ding, Hsiou-Yu] Chia Nan Univ Pharm & Sci, Dept Cosmet Sci, Tainan, Taiwan; [Lai, Jenn-Haung] Triserv Gen Hosp, Dept Med, Rheumatol Immunol & Allergy, Taipei, Taiwan; [Lin, Hang-Ching; Chang, Wen-Liang] Natl Def Med Ctr, Sch Pharm, Taipei, Taiwan in 2020.0, Cited 43.0. COA of Formula: C8H8O2. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4

A new macrocyclic diterpenoid, 4 beta,5 beta-dihydroxyovatodiolide (1), together with twenty-two known compounds (2-23) were isolated from the MeOH extract of the dried aerial parts ofAnisomeles indica(L.) O. Kuntze (Labiatae). The structure of1was established on the basis of spectral evidence. Phenylethanoids, acteoside (5) and isoacteoside (6) showed significant inhibitory to IL-2 secretion of with respect to phorbol myristate acetate and anti-CD28 monoclonal antibody co-stimulated activation of human peripheral blood T cells.

Welcome to talk about 99-93-4, If you have any questions, you can contact Chao, CL; Huang, HC; Ding, HY; Lai, JH; Lin, HC; Chang, WL or send Email.. COA 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

Computed Properties of C8H8O2. In 2020.0 POLYM CHEM-UK published article about BLOCK-COPOLYMERS; POTENTIAL APPLICATIONS; POLYMERIC MICELLES; DELIVERY; AZOBENZENE; PROBES; DESIGN; NANOPARTICLES; VESICLES; TUMOR in [Wang, Yuqing; Yu, Jiawei; Wang, Zhe; Iqbal, Shahid; Zhang, Wei; Zhang, Zhengbiao; Zhou, Nianchen; Zhu, Xiulin] Soochow Univ, State & Local Joint Engn Lab Novel Funct Polymer, Suzhou 215123, Peoples R China; [Wang, Yuqing; Yu, Jiawei; Wang, Zhe; Iqbal, Shahid; Zhang, Wei; Zhang, Zhengbiao; Zhou, Nianchen; Zhu, Xiulin] Soochow Univ, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Suzhou 215123, Peoples R China; [Wang, Yuqing; Yu, Jiawei; Wang, Zhe; Iqbal, Shahid; Zhang, Wei; Zhang, Zhengbiao; Zhou, Nianchen; Zhu, Xiulin] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China; [Zhu, Xiulin] Global Inst Software Technol, 5 Qingshan Rd, Suzhou 215163, Peoples R China in 2020.0, Cited 62.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

A near-infrared fluorescent probe plays an important role in biosensing and bioimaging because of its high efficiency, sensitivity and negligible background interference in vivo. Azobenzene derivatives demonstrate well-known sensitivity to light and are unique enzyme-responsive candidates in drug delivery and biological detection because the azo double bond can be cleaved by azoreductase. Herein, a novel near-infrared probe of an amphiphilic block copolymer with biological compatibility was synthesized. The azobenzene group attached with the near-infrared fluorescent group AzaBODIPY (boron-dipyrromethenes) linked the hydrophilic (PEG) and hydrophobic (PLA) segments to form the amphiphilic block copolymer PEG-AzaBODIPY-AZO-PLA. PEG(398)-AzaBODIPY-AZO-PLA(144) self-assembled into drug-loaded spherical micelles. The self-assemblies were non-fluorescent owing to the aggregation-induced quenching (ACQ) effect. Triggered by azoreductase, the PEG and PLA segments were disconnected due to the cleavage of the azo bond. This caused the disassembly of the micelles and the subsequent release of the encapsulated drug. Upon disassembly, the emission of the near-infrared fluorescence was activated by the elimination of the ACQ effect. Furthermore, the fluorescence intensity of the self-assemblies in solution increased continuously with drug release. The fluorescence reporting drug release demonstrates the potential applications in biosensing and controlled drug release in the colon of the human intestine.

Computed Properties of C8H8O2. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Wang, YQ; Yu, JW; Wang, Z; Iqbal, S; Zhang, W; Zhang, ZB; Zhou, NC; Zhu, XL 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

Recently I am researching about NITROGEN-CONTAINING BISPHOSPHONATES; PALLADIUM-CATALYZED PHOSPHONATION; PD(II)-CATALYZED PHOSPHORYLATION; REGIOSELECTIVE PHOSPHONATION; BIOLOGICAL EVALUATION; DIPHOSPHATE SYNTHASE; H-PHOSPHONATES; DRUG-DELIVERY; BONE; ALKYNES, Saw an article supported by the National Key Research and Development Program of China [2019YFA0905100]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21772142, 21901181, 21961142015]; Tianjin Municipal Science & Technology Commission [19JCQNJC04700]. Safety of 4′-Hydroxyacetophenone. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Cao, HQ; Liu, HN; Liu, ZY; Qiao, BK; Zhang, FG; Ma, JA. The CAS is 99-93-4. Through research, I have a further understanding and discovery of 4′-Hydroxyacetophenone

Herein we report a novel and straightforward protocol for the construction of valuable gem-BPs by means of proton-coupled electron-transfer (PCET)-triggered enamido C(sp(2))-H diphosphorylation. This reaction represents a rare example of realizing the challenging double C-P bond formation at a single carbon atom, thus providing facile access to a broad variety of structurally diverse bisphosphonates from simple enamides under silver-mediated conditions. Initial mechanistic studies demonstrated that the diphosphorylation involves two rounds of PCET-initiated radical relay process.

Welcome to talk about 99-93-4, If you have any questions, you can contact Cao, HQ; Liu, HN; Liu, ZY; Qiao, BK; Zhang, FG; Ma, JA or send Email.. Safety of 4′-Hydroxyacetophenone

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 Deep Eutectic Solvent Mediated One-Pot Synthesis of Hydrazinyl-4-Phenyl-1,3-Thiazoles WOS:000477274800001 published article about ANTIMICROBIAL ACTIVITY; 2,4-DISUBSTITUTED THIAZOLES; 3-COMPONENT SYNTHESIS; DERIVATIVES; ANTIBACTERIAL; WATER in [Kaldareh, Mahdiye Foroughi; Mokhtary, Masoud; Nikpassand, Mohammad] Islamic Azad Univ, Rasht Branch, Dept Chem, Rasht, Iran in 2021, Cited 27. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Recommanded Product: 99-93-4

One-pot synthesis of hydrazinyl-4-phenyl-1,3-thiazole derivatives was developed by three-component reaction of various ketones or aldehydes, phenacyl chloride, and thiosemicarbazid in the presence of choline chloride/urea as a deep eutectic solvent (DES) at 70 degrees C. The products formed in excellent yields over short reaction times under an environmentally friendly condition. This method develops by using an environmentally benign synthetic method along with the use of a cost-effective catalyst. The study of antibacterial activity revealed that the compounds (4j, 4k, 4l, 4m, 4s, and 4t) showed good inhibition toward Escherichia coli.

About 4′-Hydroxyacetophenone, If you have any questions, you can contact Kaldareh, MF; Mokhtary, M; Nikpassand, M or concate me.. Recommanded Product: 99-93-4

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

Dwivedi, AR; Kumar, V; Kaur, H; Kumar, N; Yadav, RP; Poduri, R; Baranwal, S; Kumar, V in [Dwivedi, Ashish Ranjan; Kumar, Vijay; Kaur, Harmeet; Kumar, Naveen; Poduri, Ramarao; Kumar, Vinod] Cent Univ Punjab, Dept Pharmaceut Sci & Nat Prod, Bathinda 151001, Punjab, India; [Yadav, Ravi Prakash; Baranwal, Somesh] Cent Univ Punjab, Sch Basic & Appl Sci, Dept Microbiol, Bathinda 151001, Punjab, India; [Kumar, Vinod] Cent Univ Punjab, Lab Organ & Med Chem, Dept Chem, Bathinda 151001, Punjab, India published Anti-proliferative potential of triphenyl substituted pyrimidines against MDA-MB-231, HCT-116 and HT-29 cancer cell lines in 2020.0, Cited 47.0. Name: 4′-Hydroxyacetophenone. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

A series of triphenyl substituted pyrimidines as analogous of colchicine and combretastatin A-4 was synthesized and evaluated for the antiproliferative potential. The compounds were screened against MDA-MB-231, HCT-116 and HT-29 cell lines using MTT assay. Most of the compounds displayed antiproliferative activity in low to sub micro molar concentration. Amongst the synthesized derivatives, compounds HK-2, HK-10 and HK-13 were found to be effective against all the three cancer cell lines. HK-2 exhibited IC50 values of 3.39 mu M, 4.78 mu M and 4.23 mu M, HK-10 showed IC50 values of 0.81 mu M, 5.89 mu M, 4.96 mu M and HK-13 showed IC50 values 3.24 mu M, 4.93 mu M and 4.73 mu M against MDA-MB-231, HCT-116 and HT-29 cancer cell lines, respectively. HK-10 was found to be the most potent compound in the series with IC50 values of 0.81 mu M against MDA-MB-231. In the cell cycle analysis, HK-2 and HK-10 showed cell arrest at G2/M phase of the cell cycle while HK-13 inhibited cell growth at the G1/G0 phase. All the three compounds showed cell death induced through apoptosis. In the docking studies, HK-2, HK-10 and HK-13 were found to fit well in the colchicine binding site of the tubulin. Some of the compounds in the current series were found to be promising against all the three cancer cell lines and may act as potent leads for further development.

Name: 4′-Hydroxyacetophenone. 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

Application In Synthesis of 4′-Hydroxyacetophenone. I found the field of Polymer Science very interesting. Saw the article Synthesis and characterization of novel fluorinated poly(ether imide)s containing pyridine and/or phenylphosphine oxide moieties published in 2019.0, Reprint Addresses Liu, XL; Sheng, SR (corresponding author), Jiangxi Normal Univ, Minist Educ, Key Lab Funct Small Organ Mol, Nanchang 330022, Jiangxi, Peoples R China.. The CAS is 99-93-4. Through research, I have a further understanding and discovery of 4′-Hydroxyacetophenone.

4-(4-Trifluoromethylphenyl)-2,6-bis[4-(4-amino-2-trifluoromethylphenoxy)phenyl]pyridine (9FPBAPP), as a new aromatic diamine, was prepared by a modified Chichibabin reaction of 4-(4-nitro-2-trifluoromethylphenoxy)acetophenone with 4-triflouromethylbenzaldehyde, followed by a catalytic reduction. A series of fluorinated poly(ether imide)s containing pyridine and/or phenylphosphine oxide moieties were prepared from bis(3-aminophenyl)phenylphosphine oxide (BAPPO), 2,2 ‘-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA), and 9FPBAPP via a conventional two-step thermal imidization procedure with various mole ratios of BAPPO and 9FPBAPP. All the polymers were amorphous and soluble in common organic solvents such as N,N-dimethylacetamide and N-methyl-2-pyrrolidone and had T-g’s of 277-285 degrees C, 5% weight loss temperature of 521-550 degrees C in nitrogen. Furthermore, high char yields and good limited oxygen index values indicated that these polymers exhibited good thermal stability and flame-retardant property. Tough and flexible polymer films also had good mechanical properties with tensile strengths of 75-99 MPa, tensile moduli of 1.1-1.6 GPa, and elongations at break of 12%-24% and low dielectric constants of 2.81-3.53 (1 MHz), as well as high optical transparency with the ultraviolet cutoff wavelength in the range of 350-384 nm.

Application In Synthesis of 4′-Hydroxyacetophenone. Welcome to talk about 99-93-4, If you have any questions, you can contact Zhang, XL; Liu, XL; Wang, QY; Huang, ZZ; Sheng, SR 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

Formula: C8H8O2. Authors Zhu, ZD; Gong, YX; Tong, WQ; Xue, WC; Gong, HG in AMER CHEMICAL SOC published article about in [Zhu, Zhaodong; Gong, Yuxin; Tong, Weiqi; Xue, Weichao; Gong, Hegui] Shanghai Univ, Ctr Supramol Chem & Catalysis, Shanghai 200444, Peoples R China; [Zhu, Zhaodong; Gong, Yuxin; Tong, Weiqi; Xue, Weichao; Gong, Hegui] Shanghai Univ, Dept Chem, Shanghai 200444, Peoples R China in 2021.0, Cited 66.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4

A nickel-catalyzed reductive coupling of aryl triflates with thiocarbonates is reported here. Both electron-rich and -deficient aryl C(sp(2))-O electrophiles as well as a class of O-tBu S-alkyl thiocarbonates are compatible with the optimized reaction conditions, as evidenced by 49 examples. The reaction also proceeds with good chemoselective cleavage of the C-O bond with regard to thioesters. This work broadens the scope of nickel-catalyzed reductive cross-electrophile coupling reactions.

Formula: C8H8O2. Welcome to talk about 99-93-4, If you have any questions, you can contact Zhu, ZD; Gong, YX; Tong, WQ; Xue, WC; Gong, HG 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

HPLC of Formula: C8H8O2. Oudjedi, K; Manso, S; Nerin, C; Hassissen, N; Zaidi, F in [Oudjedi, K.; Hassissen, N.; Zaidi, F.] Univ Bejaia, Fac Sci Nat & Vie, Dept Sci Alimentaires, Route Targa Ouzemour, Bejaia 06000, Algeria; [Manso, S.; Nerin, C.] Univ Zaragoza, Inst Invest Ingn Aragon I3A, Dept Quim Analit, Maria de Luna 3, Zaragoza 50018, Spain; [Oudjedi, K.] Ctr Rech Biotechnol CRBT, Div Biotechnol Alimentaire, BPE 73 UV 03 Ali Mendjelli Nouvelle Ville, Constantine, Algeria published New active antioxidant multilayer food packaging films containing Algerian Sage and Bay leaves extracts and their application for oxidative stability of fried potatoes in 2019.0, Cited 59.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

The antioxidant activity of Sage leaf (SL) and Bay leaf (BL) extracts was studied. Both plants were extracted using water and ethanol at different concentration, and the antioxidant activity was measured by ABTS [2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid)] radical cation scavenging and reducing power (RP) methods. In both cases 60% and 80% ethanolic extracts of Sage and Bay leaves showed the highest activity and were incorporated into multilayer films. The initial concentration for 60% ethanolic extracts of Sage and Bay leaves to scavenge 50% of free radical ABTS were 5.67 +/- 0.26 mu g x mL(-1) and 18.68 +/- 0.16 mu g x mL(-1) respectively, whereas for 80% ethanolic extracts the concentrations were 7.96 +/- 0.02 and 14.65 +/- 0.59 mu g x mL(-1) respectively. The initial concentrations of ethanolic 60% extracts of Sage and Bay leaves to allow absorbance 0.5 for reducing power were 35.38 +/- 0.19 mu g x mL(-1) and 91.43 +/- 2.84 mu g x mL(-1) respectively, while for 80% ethanolic extracts of Bay and Sage leaves were 46.01 +/- 1.21 mu g x mL(-1) and 85.47 +/- 0.9 mu g x mL(-1) respectively. Then, the multilayer films were exposed to a gas stream enriched with free radicals to evaluate the free radicals scavenging. The new packaging with 60% ethanolic Sage extract exhibited the highest activity with low percentage of hydroxylation (69.64 +/- 6.86%) followed by that with 80% ethanolic extract for both Bay (85.49 +/- 5.3%) and Sage (87.09 +/- 3.93%) leaves extracts. The ability of two active packaging built with 60% ethanolic Sage extract and 80% ethanolic Bay extract to inhibit lipid oxidation of fried potatoes was studied by measuring secondary lipid oxidation products using thiobarituric acid reactive substances (TBARS). Significant lower value of Malondialdehyde (MDA) was obtained for fried potatoes stored in active packaging built with ethanolic 60% extract of Sage and 80% ethanolic extract of Bay leaves (0.342 +/- 0.01 and 0.392 +/- 0.02 mu g MDA x g(-1) respectively) at 40 degrees C for 20 days compared to the control (0.568 +/- 0.03 mu g MDA x g(-1)). Lipid oxidation decreased 40% and 31% for packaging with 60% Sage and 80% Bay ethanolic extracts respectively. The UPLC-MS-QTOF analysis of Sage and Bay leaves extracts revealed the presence of phenolic acids, tannins, flavonoids, and terpenoids. Migration tests from active materials demonstrated the absence of migration.

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.. 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

In 2019.0 FITOTERAPIA published article about ROOTS in [Kutluay, Vahap Murat; Saracoglu, Iclal] Hacettepe Univ, Fac Pharm, Dept Pharmacognosy, TR-06100 Ankara, Turkey; [Ishiuchi, Kan’ichiro; Makino, Toshiaki] Nagoya City Univ, Grad Sch Pharmaceut Sci, Dept Pharmacognosy, Nagoya, Aichi 4678603, Japan in 2019.0, Cited 25.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. COA of Formula: C8H8O2

The phytochemical studies on the aerial parts of Digitalis davisiana Heywood led to the isolation of three undescribed phenylethanoid glycosides named as digidavisoside A (5), digidavisoside B (7), and davisoside (8), along with 9 known compounds, ferruginoside B (1), isolugrandoside (2), lugrandoside (3), maxoside (4), 3 ””-O-methylmaxoside (6), trans-lamiuside E (9), digiciliside B (10), p-hydroxyacetophenone (11), and chrysoeriol (12). For the first time compound 11 was reported for Digitalis genus. The chemotaxonomical significance of these compounds in Plantaginaceae family was evaluated and 3′-O-glucosyl substituted phenylethanoid glycosides 4-8 and 10 were found to be chemotaxonomically important for the family. Cytotoxic activity of the aqueous fraction of the methanolic extract was also tested against HEp-2 (human larynx epidermoid carcinoma) and HepG2 (human hepatocellular carcinoma) cancer cell lines. The aqueous fraction showed stronger cytotoxicity on HEp-2 cells than on HepG2. Therefore, the cytotoxic activity of 1-4, 6, 7 and 9 were tested against HEp-2 and L929 (mouse fibroblast cell) cell lines. Other isolated compounds could not be tested due to their insufficient amount. The results were evaluated in the point of structure-activity relationships. IC50 values against HEp-2 cells were established in a range of 71.9-220 mu M. Maxoside (4), isolugrandoside (2) and lugrandoside (3) showed higher cytotoxicity against HEp.2 cell line than other isolated compounds.

Welcome to talk about 99-93-4, If you have any questions, you can contact Kutluay, VM; Ishiuchi, K; Makino, T; Saracoglu, I or send Email.. COA 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