Category: 100-83-4

Computed Properties of C7H6O2. In 2019.0 J CATAL published article about ASYMMETRIC TRANSFER HYDROGENATION; CARBONYL-COMPOUNDS; CARBENE COMPLEXES; ACTIVE CATALYST; CP-ASTERISK; EFFICIENT; KETONES; REDUCTION; LIGANDS; WATER in [Pandrala, Mallesh; Resendez, Angel; Malhotra, Sanjay V.] Stanford Univ, Sch Med, Dept Radiat Oncol, Palo Alto, CA 94304 USA in 2019.0, Cited 53.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

Iridium-catalyzed transfer hydrogenation (TH) of carbonyl compounds using HCOOR (R = H, Na, NH4) as a hydrogen source is a pivotal process as it provides the clean process and is easy to execute. However, the existing highly efficient iridium catalysts work at a narrow pH; thus, does not apply to a wide variety of substrates. Therefore, the development of a new catalyst which works at a broad pH range is essential as it can gain a broader scope of utilization. Here we report highly efficient polypyridyl iridium(III) catalysts, [Ir(tPY)(L)Cl](PF6)(2) (where tpy = 2,2′:6′,2-Terpyridine, L = phen (1,10-Phenanthroline), Me(2)phen (4,7-Di methyl-1,10-phenanthroline), Me(4)phen (3,4,7,8-Tetramethyl-1,10-phenanthroline), Me(2)bpy (4,4′-Dimet hyl-2-2′-dipyridyl)) for the chemoselective reduction of aldehydes to alcohols in aqueous ethanol and sodium formate as the hydride source. The reaction can be carried out efficiently in broad pH ranges, from pH 6 to 11. These catalysts are air stable, easy to prepare using commercially available starting materials, and are highly applicable for a wide range of substrates, such as electron-rich or deficient (hetero)arenes, halogens, phenols, alkoxy, ketones, esters, carboxylic acids, cyano, and nitro groups. Particularly, acid and hydroxy groups containing aldehydes were reduced successfully in basic and acidic reaction conditions, demonstrating the efficiency of the catalyst in a broad pH range with high conversion rates under microwave irradiation. (C) 2019 Elsevier Inc. All rights reserved.

Computed Properties of C7H6O2. Bye, fridends, I hope you can learn more about C7H6O2, 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

Computed Properties of C7H6O2. In 2019.0 J CATAL published article about ASYMMETRIC TRANSFER HYDROGENATION; CARBONYL-COMPOUNDS; CARBENE COMPLEXES; ACTIVE CATALYST; CP-ASTERISK; EFFICIENT; KETONES; REDUCTION; LIGANDS; WATER in [Pandrala, Mallesh; Resendez, Angel; Malhotra, Sanjay V.] Stanford Univ, Sch Med, Dept Radiat Oncol, Palo Alto, CA 94304 USA in 2019.0, Cited 53.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

Iridium-catalyzed transfer hydrogenation (TH) of carbonyl compounds using HCOOR (R = H, Na, NH4) as a hydrogen source is a pivotal process as it provides the clean process and is easy to execute. However, the existing highly efficient iridium catalysts work at a narrow pH; thus, does not apply to a wide variety of substrates. Therefore, the development of a new catalyst which works at a broad pH range is essential as it can gain a broader scope of utilization. Here we report highly efficient polypyridyl iridium(III) catalysts, [Ir(tPY)(L)Cl](PF6)(2) (where tpy = 2,2′:6′,2-Terpyridine, L = phen (1,10-Phenanthroline), Me(2)phen (4,7-Di methyl-1,10-phenanthroline), Me(4)phen (3,4,7,8-Tetramethyl-1,10-phenanthroline), Me(2)bpy (4,4′-Dimet hyl-2-2′-dipyridyl)) for the chemoselective reduction of aldehydes to alcohols in aqueous ethanol and sodium formate as the hydride source. The reaction can be carried out efficiently in broad pH ranges, from pH 6 to 11. These catalysts are air stable, easy to prepare using commercially available starting materials, and are highly applicable for a wide range of substrates, such as electron-rich or deficient (hetero)arenes, halogens, phenols, alkoxy, ketones, esters, carboxylic acids, cyano, and nitro groups. Particularly, acid and hydroxy groups containing aldehydes were reduced successfully in basic and acidic reaction conditions, demonstrating the efficiency of the catalyst in a broad pH range with high conversion rates under microwave irradiation. (C) 2019 Elsevier Inc. All rights reserved.

Computed Properties of C7H6O2. Bye, fridends, I hope you can learn more about C7H6O2, 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

Quality Control of 3-Hydroxybenzaldehyde. Dofe, VS; Sarkate, AP; Tiwari, SV; Lokwani, DK; Karnik, KS; Kale, IA; Dodamani, S; Jalalpure, SS; Burra, PVLS in [Dofe, Vidya S.] Deogiri Coll, Dept Chem, Aurangabad 431005, Maharashtra, India; [Sarkate, Aniket P.; Karnik, Kshipra S.; Kale, Ishwari A.] Dr Babasaheb Ambedkar Marathwada Univ, Dept Chem Technol, Aurangabad 431004, Maharashtra, India; [Tiwari, Shailee, V] Durgamata Inst Pharm, Dept Pharmaceut Chem, Parbhani 431401, Maharashtra, India; [Lokwani, Deepak K.] RC Patel Inst Pharmaceut Educ & Res, Dept Pharmaceut Chem, Shirpur 425405, MS, India; [Dodamani, Suneel; Jalalpure, Sunil S.] KLE Acad Higher Educ & Res, Dr Prabhakar Kore Basic Sci Res Ctr, Belagavi 590010, Karnataka, India; [Jalalpure, Sunil S.] KLE Acad Higher Educ & Res, KLE Coll Pharm, Belagavi 590010, Karnataka, India; [Burra, Prasad V. L. S.] KLEF Univ, Dept Biotechnol, Vaddeswaram 522502, AP, India published Ultrasound assisted synthesis of tetrazole based pyrazolines and isoxazolines as potent anticancer agents via inhibition of tubulin polymerization in 2020.0, Cited 49.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

In search of new active molecules against MCF-7, A549 and HepG2, tetrazole based pyrazoline and isoxazoline derivatives under both conventional and ultrasonic irradiation method were designed and efficiently synthesized. Structures of newly synthesized compounds 5a-h and 6a-h were characterized by H-1 NMR, C-13 NMR, MS and elemental analysis. Several derivatives were found to be excellent cytotoxic against MCF-7, A549 and HepG2 cell lines characterized by lower IC50 values (0.78-3.12 mu g/mL). Compounds 5b and 5c demonstrated an antiproliferative effect comparable to that of CA-4. Western blot analysis revealed that, reported compounds accumulate more tubulin in the soluble fraction. Docking studies suggested that, binding of these compounds mimics at the colchicine site of tubulin. In vitro study revealed that the tetrazole based pyrazolines and isoxazolines may possess ideal structural requirements for further development of novel therapeutic agents.

Quality Control of 3-Hydroxybenzaldehyde. Bye, fridends, I hope you can learn more about C7H6O2, 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

An article Synthesis, anticancer activity and molecular docking studies on 1,2-diarylbenzimidazole analogues as anti-tubulin agents WOS:000489699400082 published article about COLCHICINE BINDING-SITE; BIOLOGICAL EVALUATION; COMBRETASTATIN A-4; TUBULIN; INHIBITORS; CHEMOTHERAPY; DERIVATIVES; DESIGN; SERIES in [Zhang, Ya-Liang; Yang, Rong; Xia, Lin-Ying; Man, Ruo-Jun; Chu, Yi-Chun; Wang, Zhong-Chang; Zhu, Hai-Liang] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210023, Jiangsu, Peoples R China; [Man, Ruo-Jun] Guangxi Univ Nationalities, Guangxi Biol Polysaccharide Separat Purificat & M, Nanning 530006, Peoples R China; [Jiang, Ai-Qin] Nanjing Univ, Med Sch, Nanjing 210093, Jiangsu, Peoples R China in 2019.0, Cited 29.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4. Recommanded Product: 3-Hydroxybenzaldehyde

Twenty-four 1,2-diarylbenzimidazole derivatives were designed, synthesized and biologically evaluated. It turned out that most of them were potential anticancer drugs. Among them, compound c24 showed the highest anti-tumor activity (GI(50) = 0.71-2.41 mu M against HeLa, HepG2, A549 and MCF-7 cells), and low toxicity to normal cells (CC50 > 100 mu M against L02 cells). In the microtubule binding assay, c24 showed the most potent inhibition of microtubule polymerization (IC50 = 8.47 mu M). The binding ability of compound c24 to tubulin crystal was verified by molecular docking simulation experiment. Further studies on HepG2 and HeLa cells showed that compound c24 could cause mitotic arrest of tumor cells to G2/M phase then inducing apoptosis. To sum up, compound c24 is a promising microtubule assembly inhibitor.

Welcome to talk about 100-83-4, If you have any questions, you can contact Zhang, YL; Yang, R; Xia, LY; Man, RJ; Chu, YC; Jiang, AQ; Wang, ZC; Zhu, HL or send Email.. Recommanded Product: 3-Hydroxybenzaldehyde

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

SDS of cas: 100-83-4. Recently I am researching about IN-VITRO; CORILAGIN; PLANTS, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [31772790]; Central Public-interest Scientific Institution Basal Research Fund [Y2019XK14]; Innovation Project of Chinese Academy of Agricultural Sciences [CAAS-ASTIP-2015-LIHPS]; Science and Technology Project of Gansu Province, China [18YF1NA128]. Published in ELSEVIER in AMSTERDAM ,Authors: Dai, LX; Miao, XL; Li, B; Zhang, JY; Pan, H; Shang, XF. The CAS is 100-83-4. Through research, I have a further understanding and discovery of 3-Hydroxybenzaldehyde

Adonis coerulea Maxim. presents acaricidal activity in vitro and in vivo, and inhibits AChE and other enzymes activities. However, the active compounds against Psoroptes cuniculi were still unclear. AChE, a common acaricidal and insecticidal target, plays a key role in neural conduction of mites. In this study, using surface plasmon resonance (SPR) technology, AChE was used as a target to capture the compounds from A. coerulea methanol extract (MEAC). After calculating the affinity with molecular docking, the inhibitory effect of compounds against AChE was studied. Results showed that 27 compounds were captured by AChE and identified from MEAC by LC-MS/MS. Among of these compounds, eight compounds presented the high affinity with AChE and high scores in molecular docking assay, especially for silibinin (-12.19 kcal/mol) and vitexin (-11.72 kcal/mol). Further studies showed that although these compounds have the weak cytotoxicity against C6/36 cells, silibinin, quercetin and corilagin could inhibit AChE activity with IC50 values of 40.11 mu g/mL, 46.15 mu g/mL and 50.98 mu g/mL, respectively. These results indicated that silibinin, quercetin and corilagin may be responsible for AChE inhibition which contributes to the acaricidal properties of A coerulea. This study lays the foundation for developing sensitive and sustainability methods for active compound detection from plants.

SDS of cas: 100-83-4. Bye, fridends, I hope you can learn more about C7H6O2, 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 ONE-POT SYNTHESIS; 3-COMPONENT SYNTHESIS; CHROMENE DERIVATIVES; MULTICOMPONENT; MALONONITRILE; NANOPARTICLES; BISCOUMARIN; RECOVERY; WASTE, Saw an article supported by the research council of Arak University. Safety of 3-Hydroxybenzaldehyde. Published in SPRINGER in DORDRECHT ,Authors: Sameri, F; Mobinikhaledi, A; Bodaghifard, MA. The CAS is 100-83-4. Through research, I have a further understanding and discovery of 3-Hydroxybenzaldehyde

In this work, 1,3,5,7-tetraazaadamantan-1-ium chloride (AIL) functionalized silica-coated calcium oxide hybrid nanocatalyst (CaO@SiO2@AIL) as a novel, efficient, green and recyclable heterogeneous ionic liquid catalyst was synthesized. Catalytic activity of the CaO@SiO2@AIL hybrid nanoparticles was investigated for synthesis of the pharmaceutically valuable 2-imino-2H-chromene and dihydropyrano[c]chromene derivatives. A wide range of amines and aromatic aldehydes containing either electron-withdrawing or electron-donating substituent were examined using optimized conditions to produce the desired products. 2-Imino-2H-chromenes were synthesized under solvent-free condition, and dihydropyrano[c]chromenes were prepared in aqueous medium as green conditions within short reaction times, high yields and using easy workup procedures. Structure confirmation and surface properties of the core/shell hybrid nanoparticles were considered via Fourier transform infrared spectroscopy, X-ray powder diffraction, scanning electron microscope, energy-dispersive X-ray spectroscopy, WDS map scan, thermogravimetric and elemental analyses. This IL-supported heterogeneous nanocatalyst can be reused at least six times without considerable loss of its performance.

Welcome to talk about 100-83-4, If you have any questions, you can contact Sameri, F; Mobinikhaledi, A; Bodaghifard, MA or send Email.. Safety of 3-Hydroxybenzaldehyde

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

SDS of cas: 100-83-4. In 2019.0 NEW J CHEM published article about BOVINE SERUM-ALBUMIN; ONE-POT SYNTHESIS; MOLECULAR DOCKING; HELICOBACTER-PYLORI; NATURAL-PRODUCTS; ACID; 3,4-DIHYDROPYRIMIDIN-2(1H)-ONES; EFFICIENT; CYCLOADDITION; DERIVATIVES in [Braga, Aniris Cafiero; de Fatima, Angelo] Univ Fed Minas Gerais, Dept Quim, GEQOB, Belo Horizonte, MG, Brazil; [Silva, Thamara Ferreira; Modolo, Luzia Valentina] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Bot, Grp Estudos Bioquim Plantas GEBioPlan, Belo Horizonte, MG, Brazil; [Silva Maciel, Thamilla Maria; Figueiredo, Isis Martins; Caldas Santos, Josue Carinhanha] Univ Fed Alagoas, Inst Quim & Biotecnol, Lab Instrumentacao & Desenvolvimento Quim Analit, Maceio, AL, Brazil; [Dantas da Silva, Edjan Carlos; Da Silva-Junior, Edeildo Ferreira; de Aquino, Thiago Mendonca] Univ Fed Alagoas, Inst Quim & Biotecnol, NAPRMN, Maceio, AL, Brazil in 2019.0, Cited 80.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4.

Twenty-six Biginelli adducts were synthesized through an ionic liquid-assisted synthesis with up to 92% yield. Sixteen of these Biginelli adducts were then assayed to determine their antiureolytic activity against purified urease from jack beans. The substances BA7-S, BA9-S and BA11-S were shown to be as efficient inhibitors as hydroxyurea, a positive control used in in vitro screening assay against urease. Fluorescence studies revealed that BA7-S, BA9-S, BA11-S and BA5-S possessed high binding constant values of 5.95, 6.72, 4.55, and 4.28 M-1, respectively, while BAS12-S, without substituents, showed a low value of log K-b = 2.16 M-1. In addition, in the most thermodynamically favorable BA5-S and BA7-S urease complexes, the corresponding Biginelli adducts were capable of interacting with the active site of urease through non-ionic interactions, such as hydrophobic interactions, or hydrogen and van der Waals interactions, respectively. In silico studies also supported that the BAs interact with the active site, confirming the fluorescence and kinetic assay studies, which clearly indicate that BA5-S and BA7-S are competitive inhibitors (K-i = 0.96 and 0.57 mM, respectively). In silico studies also showed that the substituents in the aromatic ring interact with Ni atoms to form a stable complex.

SDS of cas: 100-83-4. Bye, fridends, I hope you can learn more about C7H6O2, 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

Authors Jin, JK; Zheng, WX; Xia, HM; Zhang, FL; Wang, YF in AMER CHEMICAL SOC published article about HETEROCYCLIC CARBENE BORANES; FLUORINE; ALKENES; BORON; HYDRODEFLUORINATION; CYCLIZATIONS; CATALYSIS; ARYNES; AMINE in [Jin, Ji-Kang; Zheng, Wan-Xin; Xia, Hui -Min; Zhang, Feng-Lian; Wang, Yi-Feng] Univ Sci & Technol China, Ctr Excellence Mol Synth CAS, Hefei Natl Lab Phys Sci Microscale, 96 Jinzhai Rd, Hefei 230026, Anhui, Peoples R China; [Jin, Ji-Kang; Zheng, Wan-Xin; Xia, Hui -Min; Zhang, Feng-Lian; Wang, Yi-Feng] Univ Sci & Technol China, Dept Chem, 96 Jinzhai Rd, Hefei 230026, Anhui, Peoples R China; [Wang, Yi-Feng] Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China in 2019.0, Cited 57.0. Formula: C7H6O2. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4

A regioselective radical hydroboration of gem-difluoroalkenes was developed for the synthesis of alpha-difluoroalkylborons. The reaction features excellent regioselectivity, broad substrate scope, and good functional group capability. DFT calculations implicated the remarkable alpha-selectivity was driven from the kinetically and thermodynamically more favorable alpha-addition step. The resulting alpha-difluoroalkylborons could be readily converted into NHC-boranetethered monofluoroalkenes, which demonstrated unique reactivity and applicability in the synthesis of monofluoroalkene derivatives through transformations of the boron unit.

Formula: C7H6O2. Welcome to talk about 100-83-4, If you have any questions, you can contact Jin, JK; Zheng, WX; Xia, HM; Zhang, FL; Wang, YF 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

In 2020.0 CHEM PAP published article about SHAPED LIQUID-CRYSTALS; CARBOXYL CONNECTING GROUPS; SMECTIC-A PHASE; HOMOLOGOUS SERIES; LATERAL SUBSTITUENTS; MESOPHASE BEHAVIOR; LINKAGE GROUPS; POLAR ORDER; TRANSITION; MOLECULES in [Ocak, Hale; Celikel, Fulya Cagla; Eran, Belkiz Bilgin] Yildiz Tech Univ, Dept Chem, TR-34220 Istanbul, Turkey; [Ozerol, Esma Ahlatcioglu] Yildiz Tech Univ, Dept Bioengn, TR-34220 Istanbul, Turkey; [Okutan, Mustafa] Yildiz Tech Univ, Dept Phys, TR-34220 Istanbul, Turkey in 2020.0, Cited 51.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4. Quality Control of 3-Hydroxybenzaldehyde

The synthesis, mesomorphic and dielectric investigation of new unsymmetrical bent-core mesogens derived from 3-hydroxybenzoic acid central core with linked two rodlike units carrying (S)-3,7-dimethyloctyloxy group and an n-alkyloxy chain at both terminals are presented. The liquid crystalline properties of the new unsymmetrical bent-core materials have been investigated by polarizing optical microscopy and differential scanning calorimetry. New compounds with the reversed ester linking unit exhibit a monotropic or enantiotropic columnar mesophase at lower temperatures as compared to analogs with a straight chain depending on the presence of the branched (S)-3,7-dimethyloctyloxy terminal chain. Dielectric measurements for one of the bent-core mesogens, 3-[[4-[[4-(octyloxy)benzoyl]oxy]benzoyl]oxy]benzoic acid 4-[[4-((S)-3,7-dimethyloctyloxy)phenoxy]carbonyl]phenyl ester (OBDPE), have been carried out on the angular frequency range from 25.12 to 50265k rad/s at different temperatures. Thanks to dielectric measurements, real and imaginary dielectric constant, conductivity mechanism and dielectric relaxation mechanism of OBDPE were obtained. [GRAPHICS] .

About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Ocak, H; Ozerol, EA; Celikel, FC; Okutan, M; Eran, BB or concate me.. Quality Control of 3-Hydroxybenzaldehyde

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: C7H6O2. Recently I am researching about DYNAMIC KINETIC RESOLUTION; ESCHERICHIA-COLI; SUBSTRATE; MECHANISM, Saw an article supported by the Industry University Research project of Fuzhou University [2019090501]. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Wang, LC; Xu, L; Xu, XQ; Su, BM; Lin, J. The CAS is 100-83-4. Through research, I have a further understanding and discovery of 3-Hydroxybenzaldehyde

L-threonine aldolase (LTA) is a PLP-dependent enzyme that can reversibly catalyze aldol reaction of glycine and acetaldehyde to produce beta-hydroxy-alpha-amino acids. In the present work, a putative Ita gene from Actinocorallia herbida (AhLTA) was mined and over-expressed in Escherichia coli BL21 (DE3). The substrate spectrum assay indicated that AhLTA only used glycine as donor substrate and tolerated a wild range of aromatic aldehydes as acceptor substrates. It was found that the type and position of substituents in the aromatic aldehydes exerted a significant impact on the activity and stereoselectivity at beta-carbon of AhLTA. Among those substrates, AhLTA could catalyze glycine and 4-methylsulphonyl benzaldehyde (14a) to produce L-threo-4-methylsulfonylphenylserine ((2S,3R)-14b) with high conversion (94.4%) and moderate stereoselectivity (19% de). By conditional optimization, the de value of (2S, 3R)-14b was improved to 61% and the conversion was 75%. Taken together, our study suggested that AhLTA might be a promising catalyst for producing chiral beta-hydroxy-alpha-amino acids. (C) 2020 Elsevier Ltd. All rights reserved.

Welcome to talk about 100-83-4, If you have any questions, you can contact Wang, LC; Xu, L; Xu, XQ; Su, BM; Lin, J or send Email.. HPLC of Formula: C7H6O2

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