239-57-6 ((Indazolo[2,3-a]quinoline)

快速询单

结构式：

Indazolo[2,3-a]quinolineMOL文件

CAS号：

239-57-6

英文名称：

Indazolo[2,3-a]quinoline

分子式：

C₁₅H₁₀N₂

分子量：

218.253303050995

Indazolo[2,3-a]quinoline(239-57-6)名称与标识符

名称

英文别名：

Indazolo[2,3-a]quinoline;

标识符

InChIKey：

JBUBBIDKUAKQRM-UHFFFAOYSA-N

Inchi：

1S/C15H10N2/c1-4-8-14-11(5-1)9-10-15-12-6-2-3-7-13(12)16-17(14)15/h1-10H

SMILES：

N12N=C3C(=C1C=CC1=C2C=CC=C1)C=CC=C3

Indazolo[2,3-a]quinoline(239-57-6)相关文献

1. Rediscovering Bacon's hydrazine/phenylhydrazine mediated cyclization of 2,2′-dicarbonylbi(hetero)aryls: construction of (5-azo)-/indazolo[2,3-a]quinolines
Pawan S. Dhote,Chepuri V. Ramana Org. Biomol. Chem. 2022 20 636
2. Rh(iii)-catalyzed oxidative [4+2] annulation of 2-arylquinoxalines and 2-aryl-2H-indazoles with allyl alcohols
Dhananjay S. Nipate,Neha Meena,Prakash N. Swami,Krishnan Rangan,Anil Kumar Chem. Commun. 2024 60 344
3. Rh(iii)-Catalysed synthesis of cinnolinium and fluoranthenium salts using C–H activation/annulation reactions: organelle specific mitochondrial staining applications
Sivakalai Mayakrishnan,Masilamani Tamizmani,Chandrasekar Balachandran,Shin Aoki,Narayanan Uma Maheswari Org. Biomol. Chem. 2021 19 5413
4. Rh-Catalyzed regioselective C–H activation and C–C bond formation: synthesis and photophysical studies of indazolo[2,3-a]quinolines
Sundaravel Vivek Kumar,Sundaram Ellairaja,Vanaparthi Satheesh,Vairathevar Sivasamy Vasantha,Tharmalingam Punniyamurthy Org. Chem. Front. 2018 5 2630
5. Recent advances in C–H functionalization of 2H-indazoles
Zixian Yang,Jin-Tao Yu,Changduo Pan Org. Biomol. Chem. 2022 20 7746
6. A concise Friedl?nder/Buchwald–Hartwig approach to the total synthesis of quindoline, a bioactive natural indoloquinoline alkaloid, and toward the unnatural 10-methylquindoline
María V. Méndez,Sebastian O. Simonetti,Teodoro S. Kaufman,Andrea B. J. Bracca New J. Chem. 2019 43 10803
7. Pd/Cu cooperative catalysis: an efficient synthesis of (3-isoindazolyl)allenes via cross-coupling of 2-alkynyl azobenzenes and terminal alkynes
Chuan Zhu,Chao Feng,Motoki Yamane Chem. Commun. 2017 53 2606
8. Sn(ii)-Mediated facile approach for the synthesis of 2-aryl-2H-indazole-3-phosphonates and their anticancer activities
N. Sudhapriya,C. Balachandran,S. Awale,P. T. Perumal New J. Chem. 2017 41 5582
9. Rhodium-catalyzed oxidative annulation of 1H-indazoles with alkynes for the synthesis of indazolo[3,2-a]isoquinolines via C–H bond functionalization
Jian Huang,Yang Fu,Zhihong Deng,Wei Chen,Zhibin Song,Yiyuan Peng Org. Biomol. Chem. 2020 18 9863
10. Regioselective hydroarylation and arylation of maleimides with indazoles via a Rh(iii)-catalyzed C–H activation
Asim Kumar Ghosh,Sadhanendu Samanta,Payel Ghosh,Sukanya Neogi,Alakananda Hajra Org. Biomol. Chem. 2020 18 3093

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960化工网为您提供Indazolo[2,3-a]quinoline专业化合物百科信息，包括中文名，英文名，分子式，分子量，以及该化合物的CasNo.239-57-6,相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等。 WAP版:239-57-6 国际站:239-57-6

239-57-6 ((Indazolo[2,3-a]quinoline)

Indazolo[2,3-a]quinoline(239-57-6)名称与标识符

名称

标识符

Indazolo[2,3-a]quinoline(239-57-6)相关文献

目录