New explortion of C7H8O

About Benzyl Alcohol, If you have any questions, you can contact Li, J; Xu, Y; Wang, S; Zhang, H or concate me.. Name: Benzyl Alcohol

Authors Li, J; Xu, Y; Wang, S; Zhang, H in AMER CHEMICAL SOC published article about SUPPORTED GOLD NANOPARTICLES; SELECTIVE OXIDATION; PD; PALLADIUM; CATALYST; CO; STABILIZATION; DFT in [Li, Jin; Xu, Yang; Wang, Shuai; Zhang, Hui] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, POB 98, Beijing 10029, Peoples R China in 2019.0, Cited 49.0. Name: Benzyl Alcohol. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6

A series of Ni3Al-LDH-supported AuPd nanocluster (NC) catalysts AuxPdy/LDH (x/y = Au/Pd ratio upon the molar percentages of Au and Pd to the total metal; LDH: layered double hydroxide) were prepared by modified electrostatic adsorption of captopril-protected AuxPdy NCs onto the predispersed LDH support followed by proper calcination. The systematic characterizations reveal that the ultrafine AuxPdy NCs ranging from 1.4 +/- 0.5 to 1.6 +/- 0.5 nm with the Au/Pd ratios reducing from 96/4 to 61/39 are mainly dispersed on the edge of small LDH nanosheets in obtained catalysts AuxPdy/LDH. All of the catalysts AuxPdy/LDH exhibit higher aerobic oxidation activity of 1-phenylethanol than the monometallic Au-25/LDH, of which the Au87Pd13/LDH (1.5 +/- 0.5 nm) shows the highest activity with turnover frequency (TOF) of 6810 h(-1) in toluene and an extremely high performance with 131 400 h(-1) under solvent-free condition, attributed to the ultrasmall Au87Pd13 NCs, the most electron-rich Au species formed by the electron transfer from Pd to Au and Ni-OH to Au87Pd13 NCs and the strongest Au87Pd13 NCs-LDH synergistic effect. Moreover, the catalyst maintains 98% of the initial conversion of 1-phenylethanol after 10 runs and possesses good adaptability for substrate alcohols.

About Benzyl Alcohol, If you have any questions, you can contact Li, J; Xu, Y; Wang, S; Zhang, H or concate me.. Name: Benzyl Alcohol

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

Machine Learning in Chemistry about 99-93-4

Formula: C8H8O2. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Liu, HX; Chen, SC; Zhang, X; Dong, CM; Chen, YC; Liu, ZM; Tan, HB; Zhang, WM or concate me.

Recently I am researching about NATURAL-PRODUCTS; MEROTERPENOIDS; DERIVATIVES, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81773602, 41906106]; Guangdong Provincial Special Fund for Marine Economic Development Project [[2020]042]; Guangdong Special Support Program [2019TQ05Y375]; Innovation Promotion Association of CAS [2020342]; Team Project of the Natural Science Foundation of Guangdong Province [2016A030312014]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Liu, HX; Chen, SC; Zhang, X; Dong, CM; Chen, YC; Liu, ZM; Tan, HB; Zhang, WM. The CAS is 99-93-4. Through research, I have a further understanding and discovery of 4′-Hydroxyacetophenone. Formula: C8H8O2

A highly substituted phenol derivative, effphenol A (1), was isolated from the deep-sea-derived fungus Trichobotrys effuse FS524. Its complete structural assignment was established through a combination of spectroscopic analysis together with single-crystal X-ray diffraction experiments and further unequivocally confirmed by a biomimetic total synthesis. Structurally, effphenol A possesses a poly-substituted 6-5/6/6 tetracyclic ring system, which represents the first case of such a skeleton found in nature. Furthermore, the cytotoxic activity of effphenol A (1) toward four human cancer cell lines was assayed.

Formula: C8H8O2. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Liu, HX; Chen, SC; Zhang, X; Dong, CM; Chen, YC; Liu, ZM; Tan, HB; Zhang, WM 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

Simple exploration of 100-51-6

About Benzyl Alcohol, If you have any questions, you can contact Wei, JW; Zhao, L; He, C; Zheng, SJ; Reek, JNH; Duan, C or concate me.. Application In Synthesis of Benzyl Alcohol

Application In Synthesis of Benzyl Alcohol. I found the field of Chemistry very interesting. Saw the article Metal-Organic Capsules with NADH Mimics as Switchable Selectivity Regulators for Photocatalytic Transfer Hydrogenation published in 2019.0, Reprint Addresses Zhao, L; Duan, C (corresponding author), Dalian Univ Technol, Zhang Dayu Coll Chem, State Key Lab Fine Chem, Dalian 116024, Peoples R China.. The CAS is 100-51-6. Through research, I have a further understanding and discovery of Benzyl Alcohol.

Switchable selective hydrogenation among the groups in multifunctional compounds is challenging because selective hydrogenation is of great interest in the synthesis of fine chemicals and pharmaceuticals as a result of the importance of key intermediates. Herein, we report a new approach to highly selectively (>99%) reducing C=X (X = O, N) over the thermodynamically more favorable nitro groups locating the substrate in a metal-organic capsule containing NADH active sites. Within the capsule, the NADH active sites reduce the double bonds via a typical 2e(-) hydride transfer hydrogenation, and the formed excited-state NAD(+) mimics oxidize the reductant via two consecutive 1e(-) processes to regenerate the NADH active sites under illumination. Outside the capsule, nitro groups are highly selectively reduced through a typical 1e(-) hydrogenation. By combining photoinduced 1e(-) transfer regeneration outside the cage, both 1e(-) and 2e(-) hydrogenation can be switched controllably by varying the concentrations of the substrates and the redox potential of electron donors. This promising alternative approach, which could proceed under mild reaction conditions and use easy-to-handle hydrogen donors with enhanced high selectivity toward different groups, is based on the localization and differentiation of the 2e(-) and 1e(-) hydrogenation pathways inside and outside the capsules, provides a deep comprehension of photocatalytic microscopic reaction processes, and will allow the design and optimization of catalysts. We demonstrate the advantage of this method over typical hydrogenation that involves specific activation via well-modified catalytic sites and present results on the high, well-controlled, and switchable selectivity for the hydrogenation of a variety of substituted and bifunctional aldehydes, ketones, and imines.

About Benzyl Alcohol, If you have any questions, you can contact Wei, JW; Zhao, L; He, C; Zheng, SJ; Reek, JNH; Duan, C or concate me.. Application In Synthesis of Benzyl Alcohol

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

When did you first realize you had a special interest and talent inC7H8O2

About Mequinol, If you have any questions, you can contact Song, CY; Nie, JQ; Ma, C; Lu, CF; Wang, FY; Yang, GC or concate me.. Quality Control of Mequinol

Quality Control of Mequinol. Authors Song, CY; Nie, JQ; Ma, C; Lu, CF; Wang, FY; Yang, GC in ELSEVIER published article about in [Song, Chaoyang; Nie, Junqi; Ma, Chao; Lu, Cuifen; Wang, Feiyi; Yang, Guichun] Hubei Univ, Coll Chem & Chem Engn, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Minist Educ Key Lab Synth & Applicat Organ Funct, Wuhan 430062, Peoples R China in 2021, Cited 71. The Name is Mequinol. Through research, I have a further understanding and discovery of 150-76-5

1,2,3-Triazole contained conjugated porous polymers (CPPs) have recently emerged as a new class of efficient photocatalysts. To gain more insight into the excellent photocatalytic activity of this kind of CPPs, herein, we report the design and preparation of a series of 1,2,3-triazole-based CPPs via oxidative coupling polymerization to study their photocatalytic performance. These CPPs have donor-acceptor properties and 1,2,3-triazole serves as an electron acceptor. The resulting CPPs with thiophene, carbazole and diphenylamine as electron donor units, respectively, have distinct porosities and optoelectronic properties, and showed effective photocatalytic performance towards oxidative hydroxylation of arylboric acids and alkylation of vinylarenes with diethyl bromomalonate or bromoacetonitrile. The thiophene contained CPP was a more efficient photocatalyst for the catalytic reactions, which can be attributed to its smaller optical band gap and greater charge separation effi-ciency. Furthermore, PTPT has shown reliable recyclability with no significant loss in its catalytic activity.

About Mequinol, If you have any questions, you can contact Song, CY; Nie, JQ; Ma, C; Lu, CF; Wang, FY; Yang, GC or concate me.. Quality Control of Mequinol

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

More research is needed about 100-51-6

About Benzyl Alcohol, If you have any questions, you can contact Jiang, Y; Alharbi, NS; Sun, B; Qin, HL or concate me.. SDS of cas: 100-51-6

I found the field of Chemistry very interesting. Saw the article SO2F2 mediated cascade dehydrogenative Morita-Baylis-Hillman reaction of the C(sp(3))-H of primary alcohols with the C(sp(2))-H of electron-deficient olefins for the assembly of allylic alcohols published in 2019.0. SDS of cas: 100-51-6, Reprint Addresses Sun, B; Qin, HL (corresponding author), Wuhan Univ Technol, Sch Chem Chem Engn & Life Sci, Wuhan 430070, Hubei, Peoples R China.. The CAS is 100-51-6. Through research, I have a further understanding and discovery of Benzyl Alcohol

A cascade dehydrogenative Morita-Baylis-Hillman reaction of the C(sp(3))-H of primary alcohols with the C(sp(2))-H of electron-deficient olefins for forming allylic alcohols mediated by SO2F2 was developed. This method provides a mild process for the preparation of allylic alcohol moieties without the requirement of transition metals.

About Benzyl Alcohol, If you have any questions, you can contact Jiang, Y; Alharbi, NS; Sun, B; Qin, HL or concate me.. SDS of cas: 100-51-6

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

What kind of challenge would you like to see in a future of compound:100-51-6

About Benzyl Alcohol, If you have any questions, you can contact Zhang, HM; Yan, HG; Li, Q; Lin, H; Wen, XP or concate me.. SDS of cas: 100-51-6

Authors Zhang, HM; Yan, HG; Li, Q; Lin, H; Wen, XP in NATURE RESEARCH published article about in [Zhang, Huimin; Wen, Xiaopeng] Guizhou Univ, Inst Agrobioengn, Minist Educ, Key Lab Plant Resource Conservat & Germplasm Inno, Guiyang 550025, Peoples R China; [Zhang, Huimin; Wen, Xiaopeng] Guizhou Univ, Coll Forestry, Inst Forest Resources & Environm Guizhou, Guiyang 550025, Peoples R China; [Yan, Hongguang; Li, Quan] Kaili Univ, Kaili 556011, Guizhou, Peoples R China; [Lin, Hui] Ningde Normal Univ, Coll Chem & Mat, Ningde 352100, Peoples R China in 2021, Cited 52. SDS of cas: 100-51-6. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6

The floral fragrance of plants is an important indicator in their evaluation. The aroma of sweet cherry flowers is mainly derived from their essential oil. In this study, based on the results of a single-factor experiment, a Box-Behnken design was adopted for ultrasound- and microwave-assisted extraction of essential oil from sweet cherry flowers of the Brooks cultivar. With the objective of extracting the maximum essential oil yield (w/w), the optimal extraction process conditions were a liquid-solid ratio of 52 mL g(-1), an extraction time of 27 min, and a microwave power of 435 W. The essential oil yield was 1.23%, which was close to the theoretical prediction. The volatile organic compounds (VOCs) of the sweet cherry flowers of four cultivars (Brooks, Black Pearl, Tieton and Summit) were identified via headspace solid phase microextraction (SPME) and gas chromatography-mass spectrometry (GC-MS). The results showed that a total of 155 VOCs were identified and classified in the essential oil from sweet cherry flowers of four cultivars, 65 of which were shared among the cultivars. The highest contents of VOCs were aldehydes, alcohols, ketones and esters. Ethanol, linalool, lilac alcohol, acetaldehyde, (E)-2-hexenal, benzaldehyde and dimethyl sulfide were the major volatiles, which were mainly responsible for the characteristic aroma of sweet cherry flowers. It was concluded that the VOCs of sweet cherry flowers were qualitatively similar; however, relative content differences were observed in the four cultivars. This study provides a theoretical basis for the metabolism and regulation of the VOCs of sweet cherry flowers.

About Benzyl Alcohol, If you have any questions, you can contact Zhang, HM; Yan, HG; Li, Q; Lin, H; Wen, XP or concate me.. SDS of cas: 100-51-6

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

Downstream Synthetic Route Of C7H8O

About Benzyl Alcohol, If you have any questions, you can contact Dombrowski, JP; Ziegler, MS; Phadke, NM; Mansoor, E; Levine, DS; Witzke, RJ; Head-Gordon, M; Bell, AT; Tilley, TD or concate me.. Product Details of 100-51-6

An article Siloxyaluminate and Siloxygallate Complexes as Models for Framework and Partially Hydrolyzed Framework Sites in Zeolites and Zeotypes WOS:000595228100001 published article about PONNDORF-VERLEY REDUCTION; THERMOLYTIC MOLECULAR PRECURSOR; LEWIS-ACID SITES; SN-BETA ZEOLITES; TRIS(TERT-BUTOXY)SILOXY COMPLEXES; EXTRAFRAMEWORK ALUMINUM; HETEROGENEOUS CATALYSIS; CARBONYL-COMPOUNDS; CRYSTAL-STRUCTURES; BRONSTED ACIDITY in [Dombrowski, James P.; Ziegler, Micah S.; Witzke, Ryan J.; Tilley, T. Don] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA; [Dombrowski, James P.; Ziegler, Micah S.; Levine, Daniel S.; Witzke, Ryan J.; Head-Gordon, Martin; Bell, Alexis T.; Tilley, T. Don] Lawrence Berkeley Natl Lab, Chem Sci Div, 1 Cyclotron Rd, Berkeley, CA 94720 USA; [Phadke, Neelay M.; Mansoor, Erum; Bell, Alexis T.] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA; [Mansoor, Erum; Levine, Daniel S.; Head-Gordon, Martin] Univ Calif Berkeley, Kenneth S Pitzer Ctr Theoret Chem, Dept Chem, Berkeley, CA 94720 USA in 2021.0, Cited 124.0. Product Details of 100-51-6. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6

Anionic molecular models for nonhydrolyzed and partially hydrolyzed aluminum and gallium framework sites on silica, M[OSi(OtBu)(3)](4)(-) and HOM[OSi(OtBu)(3)](3)(-) (where M=Al or Ga), were synthesized from anionic chlorides Li{M[OSi(OtBu)(3)](3)Cl} in salt metathesis reactions. Sequestration of lithium cations with [12]crown-4 afforded charge-separated ion pairs composed of monomeric anions M[OSi(OtBu)(3)](4)(-) with outer-sphere [([12]crown-4)(2)Li](+) cations, and hydroxides {HOM[OSi(OtBu)(3)](3)} with pendant [([12]crown-4)Li](+) cations. These molecular models were characterized by single-crystal X-ray diffraction, vibrational spectroscopy, mass spectrometry and NMR spectroscopy. Upon treatment of monomeric [([12]crown-4)Li]{HOM[OSi(OtBu)(3)](3)} complexes with benzyl alcohol, benzyloxide complexes were formed, modeling a possible pathway for the formation of active sites for Meerwin-Ponndorf-Verley (MPV) transfer hydrogenations with Al/Ga-doped silica catalysts.

About Benzyl Alcohol, If you have any questions, you can contact Dombrowski, JP; Ziegler, MS; Phadke, NM; Mansoor, E; Levine, DS; Witzke, RJ; Head-Gordon, M; Bell, AT; Tilley, TD or concate me.. Product Details of 100-51-6

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

Extracurricular laboratory: Synthetic route of m-Methoxyphenol

About m-Methoxyphenol, If you have any questions, you can contact Xu, JC; Chen, JJ; Gao, F; Xie, SG; Xu, XH; Jin, Z; Yu, JQ or concate me.. COA of Formula: C7H8O2

Xu, JC; Chen, JJ; Gao, F; Xie, SG; Xu, XH; Jin, Z; Yu, JQ in [Xu, Jiancong; Chen, Jingjing; Gao, Feng; Xie, Shuguang; Xu, Xiaohua; Jin, Zhong] Nankai Univ, Coll Chem, State Key Lab, Tianjin 300071, Peoples R China; [Xu, Jiancong; Chen, Jingjing; Gao, Feng; Xie, Shuguang; Xu, Xiaohua; Jin, Zhong] Nankai Univ, Coll Chem, Inst Elementoorgan Chem, Tianjin 300071, Peoples R China; [Xu, Xiaohua; Jin, Zhong] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China; [Yu, Jin-Quan] Scripps Res Inst, Dept Chem, 10550 North Torrey Pines Rd, La Jolla, CA 92037 USA published Sequential Functionalization of meta-C-H and ipso-C-O Bonds of Phenols in 2019, Cited 48. COA of Formula: C7H8O2. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

The use of a template as a linchpin motif in directed remote C-H functionalization is a versatile yet relatively underexplored strategy. We have developed a template-directed approach to realizing one-pot sequential palladium-catalyzed meta-selective C-H olefination of phenols, and nickel-catalyzed ipso-C-O activation and arylation. Thus, this bifunctional template converts phenols to synthetically useful 1,3-disubstituted arenes.

About m-Methoxyphenol, If you have any questions, you can contact Xu, JC; Chen, JJ; Gao, F; Xie, SG; Xu, XH; Jin, Z; Yu, JQ or concate me.. COA of Formula: 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

The Best Chemistry compound:4-Methoxybenzaldehyde

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Kumar, I; Kumar, R; Gupta, SS; Sharma, U or concate me.. Category: indole-building-block

Category: indole-building-block. In 2021 J ORG CHEM published article about METAL-FREE; CARBONYL-COMPOUNDS; MESOPOROUS CARBON; HYDROGEN-PEROXIDE; SECONDARY-AMINES; ALCOHOLS; SOLVENT; PHOTOCATALYSIS; EFFICIENT; OXYGEN in [Kumar, Inder; Kumar, Rakesh; Gupta, Shiv Shankar; Sharma, Upendra] CSIR Inst Himalayan Bioresource & Technol, Chem Technol Div, Palampur 176061, Himachal Prades, India; [Kumar, Inder; Gupta, Shiv Shankar; Sharma, Upendra] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India in 2021, Cited 53. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

C-70 fullerene catalyzed photoinduced oxidation of benzylic amines at ambient conditions has been explored here. The developed strategy’s main feature includes the additive/oxidant-free conversion of benzylic amine to corresponding imine and aldehydes. The reaction manifests broad substrate scope with excellent function group leniency and is applicable up to the gram scale. Further, symmetrical secondary amines can also be synthesized from benzylic amine in a one-pot two-step process. Various experiments and density functional theory studies revealed that the current reaction involves the generation of reactive oxygen species, single electron transfer reaction, and benzyl radical formation as key steps under photocatalytic conditions.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Kumar, I; Kumar, R; Gupta, SS; Sharma, U or concate me.. 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

Properties and Exciting Facts About 150-19-6

Recommanded Product: m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact Wang, YL; Liu, Y; He, JH; Zhang, YT or concate me.

An article Redox-neutral photocatalytic strategy for selective C-C bond cleavage of lignin and lignin models via PCET process WOS:000497954900006 published article about PRIMARY ALCOHOL OXIDATION; VISIBLE-LIGHT; ORGANIC FRAMEWORKS; RADICAL CATIONS; CARBON-CARBON; DEPOLYMERIZATION; HYDROGENOLYSIS; TRANSFORMATION; DEGRADATION; BIOMASS in [Wang, Yinling; Liu, Yue; He, Jianghua; Zhang, Yuetao] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Jilin, Peoples R China in 2019, Cited 62. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6. Recommanded Product: m-Methoxyphenol

It remains challenging to achieve the selective cleavage of C-C bonds in lignin or lignin model compounds to produce aromatic products in high yield and selectivity. We have developed a redox-neutral photocatalytic strategy to accomplish this goal in both beta-O-4 and beta-1 lignin models at room temperature (RT) via proton-coupled electron transfer (PCET) process without any pretreatments of substrate, by adjusting the alkalinity of base to obtain a lignin models/base PCET pair with a bond dissociation free energy close to 102 kcal/mol. Without breaking down C-beta-C-gamma bond and any C-O bonds, this PCET method is 100% atom economy and produces exclusive C-alpha-C-beta bond cleavage products, such as benzaldehydes (up to 97%) and phenyl ethers (up to 96%), in high to excellent yields and selectivities. Preliminary studies indicated that the PCET strategy is also effective for the depolymerization of native lignin at RT, thus providing significantly important foundation to the depolymerization of lignin. (C) 2019 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.

Recommanded Product: m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact Wang, YL; Liu, Y; He, JH; Zhang, YT 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