Stereoselective Heterocycle Synthesis via Alkene Difunctionalization: Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation (Springer Theses) - Image 1

£96.55

Springer Stereoselective Heterocycle Synthesis via Alkene Difunctionalization: Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation (Springer Theses)

Name: Stereoselective Heterocycle Synthesis via Alkene Difunctionalization: Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation (Springer Theses)
Brand: Springer
Price: 96.55 GBP
Availability: InStock

Biochemistry

This is the most expensive it has ever been. Walk away.

£97 today · previous high £97 · all-time low £89

NEW HERE?

Amazon shows you one price. We show you all of them.

Tosheroon watches Amazon prices so you don't have to. Every product on Amazon has a price history — we make it visible. Set the price you'd actually pay, and we'll email you the second it gets there. No app, no account, one email.

WHAT'S ON THIS PAGE

↓ Price chart
when this has been cheap or pricey

↓ Forecast
where the price is heading next

↓ Statistics
all-time high & low, recent range

↑ Price alert
name your number, we'll email you

Price History & Forecast

Grey patches = out of stock. Cheaper = lower on the chart. Hover for exact prices.

Last 607 days • 607 data points (No recent data available)

Historical

Generating forecast...

Price Distribution

Price distribution over 607 days • 4 price levels

Days at Price

Current Price

Price Analysis

Most common price: £91 (523 days, 86.2%)

Price range: £89 - £97

Price levels: 4 different prices over 607 days

Description

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. From the Back Cover 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. About the Author David A. Petrone was born in Scarborough, Canada in 1989. He obtained his B.Sc. in Chemistry with Honors from the University of Guelph in 2011 and his Ph.D. in 2016 from the University of Toronto under the supervision of Prof. Mark Lautens. He was awarded both the Boehringer Ingelheim Award of Excellence in Organic Chemistry and the Chair’s Doctoral Medal for the work contained in this thesis. He is currently an NSERC postdoctoral fellow in Prof. Erick M. Carreira’s group at the Laboratory of Organic Chemistry at the ETH Zürich.

Product Specifications

Brand: Springer
Format: Paperback
ASIN: 3030084728
Category: Books > Subjects > Science, Nature & Maths > Biological Sciences > Biochemistry
Domain: Amazon UK
Release Date: 05 January 2019
Listed Since: 04 January 2019

Barcode

No barcode data available

Springer Stereoselective Heterocycle Synthesis via Alkene Difunctionalization: Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation (Springer Theses)

This is the most expensive it has ever been. Walk away.

Price History & Forecast

Price Distribution

Price Analysis

Description

Product Specifications

Barcode

Similar Products You Might Like

Heterogeneous Catalysis: A Versatile Tool for the Synthesis of Bioactive Heterocycles

Studies in Natural Products Chemistry (Volume 58)

Studies in Natural Products Chemistry (Volume 56)

Copper in N-Heterocyclic Chemistry

Studies in Natural Products Chemistry (Volume 55)

Organic Chemistry Student Study Guide and Solutions Manual

Nitrile Oxides, Nitrones and Nitronates in Organic Synthesis: Novel Strategies in Synthesis: 6 (Organic Nitro Chemistry)

Group 2 Mediated Dehydrocoupling (Springer Theses)

Wiley Oxidation of C-H Bonds - Organic Chemistry Text

Organotrifluoroborate Preparation, Coupling and Hydrolysis (Springer Theses)

With Organic Chemistrynow

C-H Activation: 292 (Topics in Current Chemistry, 292)

Development of New Radical Cascades and Multi-Component Reactions: Application to the Synthesis of Nitrogen-Containing Heterocycles (Springer Theses)

Development of New Radical Cascades and Multi-Component Reactions: Application to the Synthesis of Nitrogen-Containing Heterocycles (Springer Theses)

Wiley Denitrogenative Transformation of Nitrogen Heterocycles

Studies in Natural Products Chemistry: Bioactive Natural Products (Part J): 29 (Studies in Natural Product Chemistry): Volume 29 (Studies in Natural Products Chemistry, Volume 29)

Advances in Physical Organic Chemistry: Volume 53

Advances in Physical Organic Chemistry: Volume 50

Rhodium Catalysis: 61 (Topics in Organometallic Chemistry, 61)

Rhodium Catalysis: 61 (Topics in Organometallic Chemistry, 61)

Discovery and Development of Anti-Breast Cancer Agents from Natural Products (Natural Product Drug Discovery)

Studies in Natural Products Chemistry: Volume 73

Chiral Phosphorous Based Ligands in Earth-Abundant Transition Metal Catalysis

Comprehensive Aryne Synthetic Chemistry