![Development of novel bicyclo[1.1.1]pentanes (BCP) bioisosteres from bench stable [1.1.1]propellane precursors PhD](/themes/custom/tu_d8/images/uniprofile/link_white.svg)
36 monthsProgramme duration
28,600 GBPTuition Fee/year
31 Jul, 2026Application Deadline
Jan, Apr, Jul, OctStarting Month
Programme overview
Main Subject
Chemistry
Degree
PhD
Study Level
PHD
Study Mode
On Campus
Bicyclo[1.1.1]pentanes (BCPs) are an exciting class of strained, sp3 rich carbon. While their initial use was in the materials sector, recent impact has been in medicinal chemistry, drug development and the agrochemical sector. Their appeal is due to a unique 3-D structure, a direct consequence of its high sp3 carbon content, and has led to its use as a bioisosteres for the tert-butyl group, internal alkynes and significantly, mono- and disubstituted arenes.
Their synthesis is accomplished using hetero- or homolytic cleavage and relies on the inherent strain in the central carbon-carbon bond of [1.1.1]propellane. However, the practical isolation and storage of [1.1.1]propellane is very problematic; it is isolated as a solution in ethereal solvents, it must be cryogenically stored, and should be used before its rapid degradation.
In this project we will pioneer a stable crystalline alternatives of [1.1.1]propellane (J. Org. Chem. 2025, 90, 7712). Functionalization will be explored using several nucleophiles, providing orthogonal 1,3-disubstituted[1.1.1]bicyclopentane (BCP) precursors amenable to subsequent cross-coupling reactions (e.g., transition metal and photoredox mediated). This methodology will provide a superior synthetic approach to 1,3-disubstituted BCPs, with far less waste, as well as delivering stable crystalline BCP precursors.
This project will significantly increase the synthetic scope of BCPs compared to current strategies, as well as providing an excellent training platform to the prospective PhD candidate in our new state-of-the-art laboratories here at Loughborough.
Their synthesis is accomplished using hetero- or homolytic cleavage and relies on the inherent strain in the central carbon-carbon bond of [1.1.1]propellane. However, the practical isolation and storage of [1.1.1]propellane is very problematic; it is isolated as a solution in ethereal solvents, it must be cryogenically stored, and should be used before its rapid degradation.
In this project we will pioneer a stable crystalline alternatives of [1.1.1]propellane (J. Org. Chem. 2025, 90, 7712). Functionalization will be explored using several nucleophiles, providing orthogonal 1,3-disubstituted[1.1.1]bicyclopentane (BCP) precursors amenable to subsequent cross-coupling reactions (e.g., transition metal and photoredox mediated). This methodology will provide a superior synthetic approach to 1,3-disubstituted BCPs, with far less waste, as well as delivering stable crystalline BCP precursors.
This project will significantly increase the synthetic scope of BCPs compared to current strategies, as well as providing an excellent training platform to the prospective PhD candidate in our new state-of-the-art laboratories here at Loughborough.
Programme overview
Main Subject
Chemistry
Degree
PhD
Study Level
PHD
Study Mode
On Campus
Bicyclo[1.1.1]pentanes (BCPs) are an exciting class of strained, sp3 rich carbon. While their initial use was in the materials sector, recent impact has been in medicinal chemistry, drug development and the agrochemical sector. Their appeal is due to a unique 3-D structure, a direct consequence of its high sp3 carbon content, and has led to its use as a bioisosteres for the tert-butyl group, internal alkynes and significantly, mono- and disubstituted arenes.
Their synthesis is accomplished using hetero- or homolytic cleavage and relies on the inherent strain in the central carbon-carbon bond of [1.1.1]propellane. However, the practical isolation and storage of [1.1.1]propellane is very problematic; it is isolated as a solution in ethereal solvents, it must be cryogenically stored, and should be used before its rapid degradation.
In this project we will pioneer a stable crystalline alternatives of [1.1.1]propellane (J. Org. Chem. 2025, 90, 7712). Functionalization will be explored using several nucleophiles, providing orthogonal 1,3-disubstituted[1.1.1]bicyclopentane (BCP) precursors amenable to subsequent cross-coupling reactions (e.g., transition metal and photoredox mediated). This methodology will provide a superior synthetic approach to 1,3-disubstituted BCPs, with far less waste, as well as delivering stable crystalline BCP precursors.
This project will significantly increase the synthetic scope of BCPs compared to current strategies, as well as providing an excellent training platform to the prospective PhD candidate in our new state-of-the-art laboratories here at Loughborough.
Their synthesis is accomplished using hetero- or homolytic cleavage and relies on the inherent strain in the central carbon-carbon bond of [1.1.1]propellane. However, the practical isolation and storage of [1.1.1]propellane is very problematic; it is isolated as a solution in ethereal solvents, it must be cryogenically stored, and should be used before its rapid degradation.
In this project we will pioneer a stable crystalline alternatives of [1.1.1]propellane (J. Org. Chem. 2025, 90, 7712). Functionalization will be explored using several nucleophiles, providing orthogonal 1,3-disubstituted[1.1.1]bicyclopentane (BCP) precursors amenable to subsequent cross-coupling reactions (e.g., transition metal and photoredox mediated). This methodology will provide a superior synthetic approach to 1,3-disubstituted BCPs, with far less waste, as well as delivering stable crystalline BCP precursors.
This project will significantly increase the synthetic scope of BCPs compared to current strategies, as well as providing an excellent training platform to the prospective PhD candidate in our new state-of-the-art laboratories here at Loughborough.
Admission Requirements
6.5+
4.5+
180+
120+
65+
3.3+
Applicants should have or expect to achieve at least a 2:1 honours degree (or equivalent international qualification) in chemistry.
31 Jul 2026
3 Years
Jan
Apr
- Candidates are required to submit an essay(s) for acceptance
Tuition fees
Domestic
5,006 GBP
International
28,600 GBP
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