- UCAS course code
- F152
- UCAS institution code
- M20
Master of Chemistry (MChem)
MChem Chemistry with Medicinal Chemistry
- Typical A-level offer: A*AA including specific subjects
- Typical contextual A-level offer: AAA including specific subjects
- Refugee/care-experienced offer: AAB including specific subjects
- Typical International Baccalaureate offer: 37 points overall with 7,6,6 at HL, including specific requirements
Fees and funding
Fees
Tuition fees for home students commencing their studies in September 2025 will be £9,535 per annum (subject to Parliamentary approval). Tuition fees for international students will be £36,000 per annum. For general information please see the undergraduate finance pages.
Policy on additional costs
All students should normally be able to complete their programme of study without incurring additional study costs over and above the tuition fee for that programme. Any unavoidable additional compulsory costs totalling more than 1% of the annual home undergraduate fee per annum, regardless of whether the programme in question is undergraduate or postgraduate taught, will be made clear to you at the point of application. Further information can be found in the University's Policy on additional costs incurred by students on undergraduate and postgraduate taught programmes (PDF document, 91KB).
Scholarships/sponsorships
The University of Manchester is committed to attracting and supporting the very best students. We have a focus on nurturing talent and ability and we want to make sure that you have the opportunity to study here, regardless of your financial circumstances. For information about scholarships/bursaries/sponsorship please see our undergraduate fees pages and visit the Department website .
Course unit details:
Advanced Organic Synthesis
Unit code | CHEM40411 |
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Credit rating | 10 |
Unit level | Level 4 |
Teaching period(s) | Semester 1 |
Offered by | Department of Chemistry |
Available as a free choice unit? | No |
Overview
This course unit detail provides the framework for delivery in 21/22 and may be subject to change due to any additional Covid-19 impact.
Organometallics in synthesis (Prof Igor Larrosa, 8 lectures)
- Applications of main group metal complexes to organic synthesis
- Directed C-H metallation of organic substrates using organolithiums.
- Organocuprate chemistry
- Organogold catalysis for alkene and alkyne functionalisation
- Catalytic C-H activation using transition metals
Transition metal catalysis (Prof M Greaney, 8 lectures)
- Palladium-catalysed cross coupling using Stille, Suzuki, and related methods
- The Heck reaction
- Palladium-catalysed C-N and C-O bond formation
- C-H activation in synthesis
- Alkene and alkyne metathesis in synthesis
Total Synthesis (Dr G Crisenza, 8 lectures)
- The importance and value of total synthesis
- Planning synthesis by recognising key disconnections based on the functional groups present
- Strategic application of named and common organic reactions in complex settings
- Rationalising substrate controlled stereoselectivity
- Reagents used to interconvert common functional groups
- The power of ring forming reactionsMulticomponent and cascade reactions
Aims
- To provide an up-to-date account of modern methods in synthetic organic chemistry, with an emphasis on transition metal catalysis
- To cover key transformations in depth and to put them in context in synthesis
- To cover the strategies employed in the total synthesis of complex natural products
Learning outcomes
Students should be able to:
- Appreciate how modern synthetic organic chemistry is conducted
- Propose plausible organometallic synthetic strategies or routes to complex organic structures
- Propose suitable reagents for given transformations
- Be able to suggest mechanistic or strategic rationales for given synthetic routes
- Understand the principle mechanisms of transition metal catalysed cross coupling, C-H activation, and metathesis reactions
- Have an appreciation of the importance and value of total synthesis
Teaching and learning methods
Unseen Examination
Transferable skills and personal qualities
- Problem-solving skills that involve applying the information learned to unseen organic transformations and syntheses
- Time management and organisational skills (ability to work independently and to work efficiently and effectively)
Assessment methods
Method | Weight |
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Written exam | 100% |
Feedback methods
- Members of staff will provide written or verbal feedback on specific questions that students may have on any aspect of the course.
- In addition, a detailed set of answers will be available for all questions set by the staff members. The answer sheets will be made available in lectures and will be able to be downloaded from Blackboard.
- Staff will also give feedback on attempts made on past exam papers and will be able to provide an approximate classification.
- Students are encouraged to work through the problem sheets supplied on Blackboard and submit answers to the lecturers for feedback.
Recommended reading
- J. Clayden, N. Greeves, S. Warren, P. Wothers "Organic Chemistry" Oxford University Press
Study hours
Scheduled activity hours | |
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Assessment written exam | 2 |
Lectures | 21 |
Practical classes & workshops | 3 |
Independent study hours | |
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Independent study | 74 |
Teaching staff
Staff member | Role |
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Michael Greaney | Unit coordinator |