Name: Bioactive Heterocycles ii (en Inglés)
SKU: 62116287
Price: 2883.46 MXN
Availability: InStock
Author: Eguchi Shoji
ISBN: 9783540725916

portada Bioactive Heterocycles ii (en Inglés)

Formato

Libro Físico

Editorial

Springer

Autor

Eguchi Shoji

Idioma

Inglés

N° páginas

309

Encuadernación

Tapa Dura

ISBN13

9783540725916

Bioactive Heterocycles ii (en Inglés)

Eguchi Shoji (Autor) · Springer · Tapa Dura

Libro Nuevo Importado

Envío: 14 a 19 días háb.

$ 6,407.69$ 2,883.46

-55%

Costos de importación incluídos en el precio ✅

Libro Nuevo

Quedan más de 100 unidades

$ 2,883.46

¡Envío Gratis! Llega entre el 24 Sep y el 02 Oct a CUAUHTÉMOC, Ciudad de México. Seleccionar ubicación

Agregar a lista de deseos

Reseña del libro "Bioactive Heterocycles ii (en Inglés)"

As part of the series Topics in Heterocyclic Chemistry, this volume titled Bio- tive Heterocycles II presents comprehensive and up-to-date reviews on selected topics regarding synthetic as well as naturally occurring bioactive heterocycles. The ?rst chapter, "High Pressure Synthesis of Heterocycles Related to Bio- tive Molecules" by Kiyoshi Matsumoto, presents a unique high-pressure s- thetic methodology in heterocyclic chemistry. Basic principles and fruitful examples for pericyclic reactions, such as Diels-Alder reactions, 1,3-dipolar reactions, and also for ionic reactions, such as S and addition reactions, are N discussed. The review will be of considerable interest to heterocyclic chemists and synthetic chemists. The second chapter, "Ring Transformation of Nitropyrimidinone Leading to Versatile Azaheterocyclic Compounds" by Nagatoshi Nishiwaki and Masahiro Ariga, presents a very critical review on novel ring transformations of di- tropyridones and nitropyrimidinones based on the work of his group. - dressed in this review is the synthesis of functionalized molecules, such as nitroanilines, nitropyridines, and nitrophenols, by the ring transformation of dinitropyridones as the nitromalonaldehyde equivalent. Ring transformations of nitropyrimidinones with dinucleophiles to 4-pyridones, pyrimidines and 4-aminopyridines, and to polyfunctinal pyridones with 1,3-dicarbonyl c- pounds, etc., are also discussed. This review may attract the interest of synthetic chemists as well as heterocyclic chemists in the life science elds. The third chapter, "Synthesis of Thalidomide" by Norio Shibata, Takeshi Yamamoto and Takeshi Toru, describes a modern synthetic aspect of thali- mide.