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Training Courses

Event 

Title:
Advanced Aromatic Heterocyclic Chemistry
Subtitle:
A 3 Day Course
When:
22.09.2010 - 24.09.2010
Tutors:
Where:
Radisson Blu - Nice
Brochure:
View Brochure

Description

This course is intended to provide a thorough update of recent developments in the synthesis and subsequent transformations of heterocyclic aromatic compounds. The lectures briefly reprise ‘classical’ methods used for the synthesis of aromatic heterocycles containing nitrogen, oxygen and sulphur and build upon these concepts by focusing upon advances made in the area during the last decade. Improved classical processes and any new reactions described are thoroughly delineated in problem classes held in tutorial format.

Who Should Attend?

This course has been designed to be of benefit to a wide range of industrial chemists, specifically those already familiar with the principles of aromatic heterocyclic (‘heteroaromatic’) chemistry or for those who have already attended the “Essential Aromatic Heterocyclic Chemistry” or “Heterocyclic Synthesis in Modern Chemistry” courses.
This course is suitable for scientists at graduate level and above. 

Programme

Introduction

Comparison of strategies for heteroaromatic synthesis:
‘classical’ methods
transition-metal catalysed processes
modern methods

Recent Developments in the Synthesis and Reactions of:

Monocyclic, five membered monoheteroaromatic rings:
pyrroles, furans, thiophenes

Bicyclic, five-membered monoheteroaromatic rings:
indoles, isoindoles,
benzofurans, isobenzofurans,
benzothiophenes and isobenzothiophenes

Mono- and bicyclic, five-membered diheteroraomatic rings:
imidazoles, pyrazoles,
benzimidazoles, benzpyrazoles,
oxazoles, isoxazoles,
benzoxazoles, benzisoxazoles
thiazoles and isothiazoles,
benzothiazoles

Monocyclic, five membered triheteroaromatic rings:
triazoles, oxadiazoles, thiadiazoles

Monocyclic, five-membered tetraheteroaromatic rings:
tetrazoles

Mono- and bicyclic, six-membered monoheteroaromatic rings:
pyridines,
quinolines and isoquinolines

Mono- and bicyclic, six-membered diheteroaromatic rings:
pyrimidines, pyrazines, pyridazines,
quinoxalines, quinazolines and cinnolines

Fee Info

Course Fee:
£1225
Multi Discount:
SAVE 5% for 2 attendees and 15% for 3 attendees

Venue

Radisson BluMap
Venue:
Radisson Blu   -   Website
Street:
223 Promenade des Anglais
Postcode / ZIP:
06200
City:
Nice
State:
French Riviera
Country:
Country: fr

Description

The Radisson Blu, on the Cote d'Azur(the French Riviera), has a sea front location and enjoys a privileged position on the famous Promenade des Anglais, facing the Baie des Anges and the Mediterranean Sea. Centrally located, the Radisson Blu Hotel is easily accessible, being 5 minutes from Nice International Airport, 15 minutes from the central station and 5 minutes from the motorway. The resort style hotel has an elegant restaurant, coffee shop, pool side cafe, piano bar with live entertainment, and concierge with good services. The hotel offers 329 fully-equipped rooms and suites.

The hotel is holding standard rooms for us at a discounted rate. Scientific Update is contractually obligated to certain financial goals with the hotel.  Your reservation is greatly appreciated, as it helps to meet our agreement.  Please make your reservation soon in order to secure the reduced group rate.

Directions:

Nice International Airport is about 5 minutes from the hotel, the Central Station is about 15 minutes and the motorway approximately 5 minutes from the hotel.