Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Chemical Transformations Involving N-tosylhydrazones

View through CrossRef
<div style="text-align:justify;"> N-Tosylhydrazones are a class of readily available and stable diazo pre-cursors that have been widely used in organic synthesis. Since 2012, there have been numerous reports on the application of N-Tosylhydrazones as starting materials for cross-coupling, insertion, alkenylation, alkynylation and other types of reactions. In particular, the construction of structurally complex functional molecular skeletons by one-pot and cascade reactions proved to be very important in this field. Focusing on the construction of the core skeleton of functional fine chemicals, the team has carried out green synthesis and catalytic reaction studies of fine chemicals, achieved effective synthesis of high value-added fine chemicals, obtained a series of new systems of N-tosylhydrazones involved in the formation of C-C and C=C; realised the high efficiency in the preparation of diarylmethane, triarylme-thane, aryl-substituted olefins and thiazole derivatives, and laid the founda-tion of the application of the fine organic synthesis technology in the field of pharmaceuticals. This has laid a solid foundation for the application of fine organic synthesis technology in the fields of pharmaceutical intermediates, agrochemicals and optoelectronic materials, forming a distinctive research direction of fine chemical synthesis technology and a stable R&amp;D team, and improved the technical level of preparation of high value-added fine chemicals. </div> <div style="text-align:justify;"> This book can be used as a reference for workers in organic chemistry of N- tosylhydrazones, pharmaceutical synthesis and other fields, as well as teachers and students of related universities and research institutes. </div>
Scientific Research Publishing
Title: Chemical Transformations Involving N-tosylhydrazones
Description:
<div style="text-align:justify;"> N-Tosylhydrazones are a class of readily available and stable diazo pre-cursors that have been widely used in organic synthesis.
Since 2012, there have been numerous reports on the application of N-Tosylhydrazones as starting materials for cross-coupling, insertion, alkenylation, alkynylation and other types of reactions.
In particular, the construction of structurally complex functional molecular skeletons by one-pot and cascade reactions proved to be very important in this field.
Focusing on the construction of the core skeleton of functional fine chemicals, the team has carried out green synthesis and catalytic reaction studies of fine chemicals, achieved effective synthesis of high value-added fine chemicals, obtained a series of new systems of N-tosylhydrazones involved in the formation of C-C and C=C; realised the high efficiency in the preparation of diarylmethane, triarylme-thane, aryl-substituted olefins and thiazole derivatives, and laid the founda-tion of the application of the fine organic synthesis technology in the field of pharmaceuticals.
This has laid a solid foundation for the application of fine organic synthesis technology in the fields of pharmaceutical intermediates, agrochemicals and optoelectronic materials, forming a distinctive research direction of fine chemical synthesis technology and a stable R&amp;D team, and improved the technical level of preparation of high value-added fine chemicals.
</div> <div style="text-align:justify;"> This book can be used as a reference for workers in organic chemistry of N- tosylhydrazones, pharmaceutical synthesis and other fields, as well as teachers and students of related universities and research institutes.
</div>.

Related Results

The computational magic of the ventral stream
The computational magic of the ventral stream
AbstractI argue that the sample complexity of (biological, feedforward) object recognition is mostly due to geometric image transformations and conjecture that a main goal of the v...
Highly Regioselective Synthesis of 3,5-Substituted Pyrazoles from Bromovinyl Acetals and N-Tosylhydrazones
Highly Regioselective Synthesis of 3,5-Substituted Pyrazoles from Bromovinyl Acetals and N-Tosylhydrazones
A regioselective synthesis of 3,5-disubstituted pyrazoles was achieved by 1,3-dipolar cycloaddition of diazo compounds, generated in situ from N-tosylhydrazones, with unactivated b...
GLOBAL TRANSFORMATIONS OF INTERNATIONAL ECONOMIC RELATIONS
GLOBAL TRANSFORMATIONS OF INTERNATIONAL ECONOMIC RELATIONS
The issues related to the substantiation of ways and directions of global transformations of international economic relations (IER) are of bilateral scientific and practical releva...
(Invited) Chemical Sensing in the Big Data Era: How and Where Does the Chemical World Store Its Information?
(Invited) Chemical Sensing in the Big Data Era: How and Where Does the Chemical World Store Its Information?
Introduction In recent years, data analytics have emerged as an important tool for understanding many business and societal trends, and this has bee...
Weighted Radon transforms and their applications
Weighted Radon transforms and their applications
Transformations de Radon pondérées et leurs applications Cette thèse est consacrée à l'étude des problèmes inverses des transformations de Radon pondérées dans les ...
Copper catalyzed Reduction coupling of N-tosylhydrazones with Anilines in water
Copper catalyzed Reduction coupling of N-tosylhydrazones with Anilines in water
This study presents a novel and environmentally friendly approach for synthesizing N-(1phenylethyl)aniline derivatives via reductive coupling of N-tosylhydrazones with anilines in ...
Carbenylative Buchwald-Hartwig Coupling of Aryl Halides, N-Tosylhydrazones, and Anilines
Carbenylative Buchwald-Hartwig Coupling of Aryl Halides, N-Tosylhydrazones, and Anilines
A Pd/Cu cocatalyzed synthesis of N-benzhydryl amines from aryl halides (electrophiles), N-tosylhydrazones (carbene equivalents), and anilines (nucleophiles) has been developed. The...
Block Copolymers by Multi‐Mode Polymerizations
Block Copolymers by Multi‐Mode Polymerizations
Abstract The sections in this article are Introduction Coupling Methods Transfo...

Back to Top