CH5611 Asymmetric Synthesis
Academic year
2024 to 2025 Semester 1
Curricular information may be subject to change
Further information on which modules are specific to your programme.
Key module information
SCOTCAT credits
10
SCQF level
SCQF level 11
Availability restrictions
Not automatically available to General Degree students
Planned timetable
To be arranged.
Module coordinator
Prof A D Smith
Module Staff
Prof A D Smith, Dr C P Johnston
Module description
This module discusses the methods available for the synthesis of chiral compounds. After a detailed introduction to the specialised terminology and analytical methods used, the main methods using chiral auxiliaries, chiral reagents and chiral catalysts will be described. This will then be combined with a consideration of synthetic strategy and total syntheses of several complex chiral compounds will be discussed.
Relationship to other modules
Pre-requisites
BEFORE TAKING THIS MODULE YOU MUST ( PASS 1 MODULE FROM {CH2601, CH2603} AND PASS AT LEAST 1 MODULE FROM {CH2501, CH2701} ) OR ( PASS 2 MODULES FROM {CH2501, CH2701} AND PASS CH1601 OR PASS CH1202 )
Assessment pattern
2-hour Written Examination = 100%
Re-assessment
Oral Re-assessment = 100%
Learning and teaching methods and delivery
Weekly contact
2 - 3 lectures per week over 9 - 10 weeks (within Weeks 1-11) and 2 - 3 tutorials in total.
Scheduled learning hours
20
Guided independent study hours
80
Intended learning outcomes
- Be aware of the relative importance of chiral auxiliaries, reagents and catalysts in modern synthesis, and be able to propose suitable uses for the examples studied.
- Formulate stereochemical models that explain the observed diastereoselectivity or enantioselectivity of a range of asymmetric reactions.
- Use the reactions taught, along with knowledge of other well-known organic reactions to suggest a catalytic asymmetric synthesis of some relatively simple chiral molecules.
- Use the principles taught to consider unseen examples of asymmetric reactions, and be able to select the appropriate principles, and then apply them and hence rationalise the stereoselectivity of these reactions
- Understand the key topics highlighted in the lectures and support material.