Category: 80-08-0

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 80-08-0, Name is Dapsone, molecular formula is C12H12N2O2S. In an article, author is Liu, Jiarun,once mentioned of 80-08-0, Quality Control of Dapsone.

Direct Oxidative Dearomatization of Indoles with Aromatic Ketones: Rapid Access to 2,2-Disubstituted Indolin-3-ones

A metal-free oxidative dearomatization of indoles with aromatic ketones mediated by TEMPO oxoammonium salt is described. The dearomatization proceeds smoothly and displays a broad substrate scope with respect to both indoles and aromatic ketones in the presence of H2SO4, affording the corresponding 2,2-disubstituted indolin-3-ones in good yields.

Interested yet? Keep reading other articles of 80-08-0, you can contact me at any time and look forward to more communication. Quality Control of Dapsone.

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 an article, author is Mao, Jianyou, once mentioned the application of 80-08-0, Recommanded Product: 80-08-0, Name is Dapsone, molecular formula is C12H12N2O2S, molecular weight is 248.3, MDL number is MFCD00007887, category is indole-building-block. Now introduce a scientific discovery about this category.

Synthesis of Indoles through Domino Reactions of 2-Fluorotoluenes and Nitriles

Indoles are essential heterocycles in medicinal chemistry, and therefore, novel and efficient approaches to their synthesis are in high demand. Among indoles, 2-aryl indoles have been described as privileged scaffolds. Advanced herein is a straightforward, practical, and transition-metal-free assembly of 2-aryl indoles. Simply combining readily available 2-fluorotoluenes, nitriles, LiN(SiMe3)(2), and CsF enables the generation of a diverse array of indoles (38 examples, 48-92 % yield). A range of substituents can be introduced into each position of the indole backbone (C4 to C7, and aryl groups at C2), providing handles for further elaboration.

If you are interested in 80-08-0, you can contact me at any time and look forward to more communication. Recommanded Product: 80-08-0.

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

Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. In an article, author is Wang, Ting-Ting, once mentioned the application of 80-08-0, Name is Dapsone, molecular formula is C12H12N2O2S, molecular weight is 248.3, MDL number is MFCD00007887, category is indole-building-block. Now introduce a scientific discovery about this category, Recommanded Product: 80-08-0.

Versatile synthesis of functionalized beta- and gamma-carbolines via Pd-catalyzed C-H addition to nitriles/cyclization sequences

The first example of versatile synthesis of functionalized beta-carbolines and gamma-carbolines via redox-free Pd-catalyzed C-H addition of indole to nitrile/cyclization sequences is reported. A wide range of functionalized beta-carbolines and gamma-carbolines can be prepared from readily accessible indoles and nitriles in good to excellent yields under the optimal conditions.

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 80-08-0, Recommanded Product: 80-08-0.

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