4.6 Article

PhI(OAc)2-mediated intramolecular oxidative C-N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Chemistry, Organic

I+/TBHP Catalysis For Tandem Oxidative Cyclization To Indolo[2,3-b]quinolines

Muhammet Uyanik et al.

Summary: A chemoselective tandem oxidative cyclization/aromatization of indole derivatives tethered to aniline sulfonamides was reported using catalytic tetrabutylammonium iodide and TBHP under nearly neutral conditions at room temperature. The corresponding indolo[2,3-b]quinolines could be easily isolated in pure form via simple filtration, leading to the natural product quinindoline. Control experiments showed the generation of both ionic and radical active species in situ under mild conditions for chemoselective oxidative transformations.

ASIAN JOURNAL OF ORGANIC CHEMISTRY (2021)

Article Chemistry, Multidisciplinary

Oxidation of Nonactivated Anilines to Generate N-Aryl Nitrenoids

Tianning Deng et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2020)

Article Chemistry, Organic

Palladium-Catalyzed Dual Annulation: A Method for the Synthesis of Norneocryptolepine

Li-Hsuan Yeh et al.

ORGANIC LETTERS (2019)

Review Chemistry, Organic

Methods of synthesis of natural indoloquinolines isolated from Cryptolepis sanguinolenta

Oleg N. Nadein et al.

CHEMISTRY OF HETEROCYCLIC COMPOUNDS (2019)

Article Chemistry, Organic

Superbase-promoted selective carbon-carbon bond cleavage driven by aromatization

Can Liu et al.

ORGANIC & BIOMOLECULAR CHEMISTRY (2019)

Article Chemistry, Organic

An efficient iron-promoted synthesis of 6H-indolo [2,3-b]quinolines and neocryptolepine derivatives

Zicong Yan et al.

ORGANIC & BIOMOLECULAR CHEMISTRY (2016)

Article Chemistry, Medicinal

The synthesis of indolo[2,3-b]quinoline derivatives with a guanidine group: Highly selective cytotoxic agents

Katarzyna Sidoryk et al.

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2015)

Review Chemistry, Multidisciplinary

Chiral Hypervalent Iodine Reagents: Synthesis and Reactivity

Alejandro Parra et al.

CHEMISTRY-A EUROPEAN JOURNAL (2013)

Article Chemistry, Medicinal

New derivatives of 11-methyl-6-[2-(dimethylamino)ethyl]-6H-indolo[2,3-b]quinoline as cytotoxic DNA topoisomerase II inhibitors

Wojciech Luniewski et al.

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2012)

Article Chemistry, Multidisciplinary

Benziodoxole-based hypervalent iodine reagents for atom-transfer reactions

Jonathan P. Brand et al.

CHEMICAL COMMUNICATIONS (2011)

Review Biochemistry & Molecular Biology

Indoloquinolines as Scaffolds for Drug Discovery

J. Lavrado et al.

CURRENT MEDICINAL CHEMISTRY (2010)

Article Chemistry, Organic

Efficient Syntheses of the Unknown Quinolino[2,3-c]cinnolines; Synthesis of Neocryptolepines

Makhluf J. Haddadin et al.

ORGANIC LETTERS (2010)

Article Chemistry, Medicinal

Synthesis and Antiplasmodial Activity of Aminoalkylamino-Substituted Neocryptolepine Derivatives

Ibrahim El Sayed et al.

JOURNAL OF MEDICINAL CHEMISTRY (2009)

Review Chemistry, Multidisciplinary

Chemistry of Polyvalent Iodine

Viktor V. Zhdankin et al.

CHEMICAL REVIEWS (2008)

Article Plant Sciences

Jusbetonin, the first indolo[3,2-b]quinoline alkaloid glycoside, from Justicia betonica

GV Subbaraju et al.

JOURNAL OF NATURAL PRODUCTS (2004)