203,79 €
Stereoselective Heterocycle Synthesis via Alkene Difunctionalization
Stereoselective Heterocycle Synthesis via Alkene Difunctionalization
  • Išparduota
Stereoselective Heterocycle Synthesis via Alkene Difunctionalization
Stereoselective Heterocycle Synthesis via Alkene Difunctionalization
El. knyga:
203,79 €
This book investigates the use of palladium modified by bulky ligands as catalysts for new chemical transformations that rapidly assemble several classes of complex heterocyles. It documents the development of new chemical reactions involving carbon-carbon (C¿C) and carbon-halogen (C¿X) bond formation in the context of alkene difunctionalization and dearomatization reactions. Due to the ubiquity of heterocycles in bioactive natural products and life-improving pharmaceutical treatments, a long-t…

Stereoselective Heterocycle Synthesis via Alkene Difunctionalization (el. knyga) (skaityta knyga) | knygos.lt

Atsiliepimai

Aprašymas

This book investigates the use of palladium modified by bulky ligands as catalysts for new chemical transformations that rapidly assemble several classes of complex heterocyles. It documents the development of new chemical reactions involving carbon-carbon (C¿C) and carbon-halogen (C¿X) bond formation in the context of alkene difunctionalization and dearomatization reactions. Due to the ubiquity of heterocycles in bioactive natural products and life-improving pharmaceutical treatments, a long-term goal for synthetic organic chemists has been to develop novel and creative heterocycle syntheses that illicit a high degree of product diversity and are characterized by mild reaction conditions and limited waste production. A considerable fraction of leading pharmaceutical drugs contain at least one heterocycle within their chemical structure, and their prevalence in these technologies is strong evidence that the fundamental curiosities of organic chemistry lead to real-world solutions for the health and wellness of the global population.

203,79 €
Prisijunkite ir už šią prekę
gausite
2,04 Knygų Eurų! ?

Elektroninė knyga:
Atsiuntimas po užsakymo akimirksniu! Skirta skaitymui tik kompiuteryje, planšetėje ar kitame elektroniniame įrenginyje.

Mažiausia kaina per 30 dienų: 203,79 €

Mažiausia kaina užfiksuota: Kaina nesikeitė


This book investigates the use of palladium modified by bulky ligands as catalysts for new chemical transformations that rapidly assemble several classes of complex heterocyles. It documents the development of new chemical reactions involving carbon-carbon (C¿C) and carbon-halogen (C¿X) bond formation in the context of alkene difunctionalization and dearomatization reactions. Due to the ubiquity of heterocycles in bioactive natural products and life-improving pharmaceutical treatments, a long-term goal for synthetic organic chemists has been to develop novel and creative heterocycle syntheses that illicit a high degree of product diversity and are characterized by mild reaction conditions and limited waste production. A considerable fraction of leading pharmaceutical drugs contain at least one heterocycle within their chemical structure, and their prevalence in these technologies is strong evidence that the fundamental curiosities of organic chemistry lead to real-world solutions for the health and wellness of the global population.

Atsiliepimai

  • Atsiliepimų nėra
0 pirkėjai įvertino šią prekę.
5
0%
4
0%
3
0%
2
0%
1
0%
(rodomas nebus)
[{"option":"174","probability":1,"style":{"backgroundColor":"#f2f2f2"},"image":{"uri":"\/uploads\/images\/wheel_of_fortune\/69738c2a550eb1769180202.png","sizeMultiplier":0.6,"landscape":true,"offsetX":-50}},{"option":"173","probability":1.3,"style":{"backgroundColor":"#d91e2d"},"image":{"uri":"\/uploads\/images\/wheel_of_fortune\/69738c13edaf41769180179.png","sizeMultiplier":0.6,"landscape":true,"offsetX":-50}},{"option":"172","probability":1.6,"style":{"backgroundColor":"#f2f2f2"},"image":{"uri":"\/uploads\/images\/wheel_of_fortune\/69738c00656611769180160.png","sizeMultiplier":0.6,"landscape":true,"offsetX":-50}},{"option":"171","probability":1.5,"style":{"backgroundColor":"#d91e2d"},"image":{"uri":"\/uploads\/images\/wheel_of_fortune\/6979c7e026ae11769588704.png","sizeMultiplier":0.6,"landscape":true,"offsetX":-50}},{"option":"170","probability":1.5,"style":{"backgroundColor":"#f2f2f2"},"image":{"uri":"\/uploads\/images\/wheel_of_fortune\/69738bd43f5c21769180116.png","sizeMultiplier":0.6,"landscape":true,"offsetX":-50}},{"option":"169","probability":1.6,"style":{"backgroundColor":"#d91e2d"},"image":{"uri":"\/uploads\/images\/wheel_of_fortune\/69738b882df611769180040.png","sizeMultiplier":0.6,"landscape":true,"offsetX":-50}},{"option":"167","probability":1.4,"style":{"backgroundColor":"#f2f2f2"},"image":{"uri":"\/uploads\/images\/wheel_of_fortune\/69738b6e6274b1769180014.png","sizeMultiplier":0.6,"landscape":true,"offsetX":-50}},{"option":"166","probability":0.1,"style":{"backgroundColor":"#d91e2d"},"image":{"uri":"\/uploads\/images\/wheel_of_fortune\/69738b36427321769179958.png","sizeMultiplier":0.6,"landscape":true,"offsetX":-50}}]