Name: Synthesis of Narbonolide, muamvitin and (s) - (5)-[(s)-6-hyrdoxyoctyl] (en Inglés)
Price: 412879.00 COP
Availability: InStock
Author: Reddy, B. Jagan Mohan ; Ranjitha, K. V. B. ; Kavitha, A.
ISBN: 9786202564328

portada Synthesis of Narbonolide, muamvitin and (s) - (5)-[(s)-6-hyrdoxyoctyl] (en Inglés)

Formato

Libro Físico

Autor

A. Kavitha

B. Jagan Mohan Reddy

K. V. B. Ranjitha

Editorial

LAP Lambert Academic Publishing

Idioma

Inglés

N° páginas

164

Encuadernación

Tapa Blanda

Dimensiones

22.9 x 15.2 x 1.0 cm

Peso

0.25 kg.

ISBN13

9786202564328

Categorías

Química orgánica

Synthesis of Narbonolide, muamvitin and (s) - (5)-[(s)-6-hyrdoxyoctyl] (en Inglés)

A. Kavitha (Autor) · B. Jagan Mohan Reddy (Autor) · K. V. B. Ranjitha (Autor) · LAP Lambert Academic Publishing · Tapa Blanda

Libro Nuevo

$ 412.879

$ 635.199

Ahorras: $ 222.320

35% descuento

Envío normal

Origen: Estados Unidos (Costos de importación incluídos en el precio)

Se enviará desde nuestra bodega entre el Viernes 09 de Agosto y el Viernes 23 de Agosto.

Lo recibirás en cualquier lugar de Colombia entre 1 y 5 días hábiles luego del envío.

Reseña del libro "Synthesis of Narbonolide, muamvitin and (s) - (5)-[(s)-6-hyrdoxyoctyl] (en Inglés)"

The present invention provides methods and reagents relating to the PKS gene cluster for the polyketide antibiotics known as narbomycin and picromycin. Narbomycin is produced in Streptomyces narbonensis and both narbomycin and picromycin are produced in S. venezuelae. We have completed the formal synthesis of Narbonolide by using Yamaguchi esterification protocol. Muamvatin represents the first example of a naturally occurring 2,4,6-trioxaadamantane ring skeleton. Pulmonate molluscs of the genus Siphonaria are known for their characteristic production of polypropionate metabolites containing either a hydroxylated pyrone or ketal functionality. The formal synthesis of Muamvatin has been achieved in a stereocontrolled manner by silyltriflate mediated opening of epoxy alcohol and desymmetrization of the meso-bicyclic dihydrofuran using an asymmetric hydroboration. This synthetic sequence provides an easy access to the construction of the key fragments of Muamvatin.