Name: Synthesis of new Organic Molecules Via MCR Strategy (en Inglés)
SKU: 56781987
Price: 97820.00 CLP
Availability: InStock
Author: Sudharsan Reddy, Sirigi Reddy ; Vasu Govardhana Reddy, Peddiahgari
ISBN: 9786205491706

portada Synthesis of new Organic Molecules Via MCR Strategy (en Inglés)

Synthesis of new Organic Molecules Via MCR Strategy (en Inglés)

Formato

Libro Físico

Autor

Sirigi Reddy Sudharsan Reddy

Peddiahgari Vasu Govardhana Reddy

Editorial

LAP Lambert Academic Publishing

Idioma

Inglés

N° páginas

156

Encuadernación

Tapa Blanda

Dimensiones

22.9x15.2x0.9 cm

Peso

0.24 kg.

ISBN13

9786205491706

Categorías

Química orgánica

Synthesis of new Organic Molecules Via MCR Strategy (en Inglés)

Sirigi Reddy Sudharsan Reddy (Autor) · Peddiahgari Vasu Govardhana Reddy (Autor) · LAP Lambert Academic Publishing · Tapa Blanda

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Reseña del libro "Synthesis of new Organic Molecules Via MCR Strategy (en Inglés)"

Over the past two decades, significant progress developed in this direction by introducing a plethora of novel approaches such as combinatorial chemistry, multicomponent reactions, microwave and ultrasound-assisted reactions, solid phase syntheses etc. Among the multicomponent reactions (MCRs), those that involve three or more reactants reacting to each other in resulting one major specified product via one pot have been attracting much attention due to their obvious synthetic utility and numerous advantages such as minimization of the amounts of reagents, solvents, catalyst loading, easy to carry out, atom economy no requirement of isolation and purification of the intermediates, which dramatically decrease the amounts of the chemical waste, time investment and obtaining products in higher yields: when Alexandcompared with the corresponding linear multi-step synthesis. The current study is to develop new and practical methodologies for the synthesis of a broad variety of biologically active α-aminonitriles (using propylphosphonic acid anhydride), alkyl/aryl aminophenols (using chitosan), 2-amino substituted 1,3,4-oxadiazoles (using graphene oxide) and 5-aryl pyrimidoquinolines.