The University of Bristol

2011 ◽  
pp. 37-39
Author(s):  
John Howie ◽  
Michael Whitfield
Keyword(s):  
University Of Bristol ◽  
The University

scholarly journals Development and delivery of a work experience week programme for mechanical engineering

2020 ◽  
pp. 030641902098104
Author(s):  
A Gonzalez-Buelga ◽  
I Renaud-Assemat ◽  
B Selwyn ◽  
J Ross ◽  
I Lazar
Keyword(s):  
Work Experience ◽  
Mechanical Engineering ◽  
Engineering Students ◽  
Impact Analysis ◽  
Legal Term ◽  
Stage 4 ◽  
Engineering Design Problem ◽  
Hands On ◽  
University Of Bristol ◽  
The University

This paper focuses on the development, delivery and preliminary impact analysis of an engineering Work Experience Week (WEW) programme for KS4 students in the School of Civil, Aerospace and Mechanical Engineering (CAME) at the University of Bristol, UK. Key stage 4, is the legal term for the two years of school education which incorporate GCSEs in England, age 15–16. The programme aims to promote the engineering profession among secondary school pupils. During the WEW, participants worked as engineering researchers: working in teams, they had to tackle a challenging engineering design problem. The experience included hands-on activities and the use of state-of-the-art rapid prototyping and advanced testing equipment. The students were supervised by a group of team leaders, a diverse group of undergraduate and postgraduate engineering students, technical staff, and academics at the School of CAME. The vision of the WEW programme is to transmit the message that everybody can be an engineer, that there are plenty of different routes into engineering that can be taken depending on pupils’ strengths and interests and that there are a vast amount of different engineering careers and challenges to be tackled by the engineers of the future. Feedback from the participants in the scheme has been overwhelmingly positive.

scholarly journals On the impact of the Bristol ChemLabS’ outreach programme on admissions to the School of Chemistry

2011 ◽  
pp. 22-26
Author(s):  
A J Shaw ◽  
T G Harrison ◽  
K L Shallcross ◽  
S J Williams ◽  
D E Shallcross
Keyword(s):  
Sample Size ◽  
Outreach Program ◽  
Outreach Programme ◽  
Dramatic Rise ◽  
University Of Bristol ◽  
The University ◽  
Entry Qualifications ◽  
The Impact ◽  
S Application

Analysis of the average number of applicants received from schools that engaged in the Bristol ChemLabS Outreach program prior to a student‟s application with those that did not engage, shows a significant increase in applicants from engaged schools. The significance is weaker when just Post 16 students are considered but this is almost certainly due to a smaller sample size. When this analysis was inspected in terms of the distance of the school from the University of Bristol, there was an increase in the number of applicants from engaged schools irrespective of distance. However, a statistically significant increase was observed for schools within 50 miles of the University from an analysis of just Post 16 students. Students who applied to the department from an engaged school were more likely to accept an offer and also to make the department their firm acceptance. A slightly higher number of applications that were rejected came from engaged schools too. There are two possible reasons; first, the engagement may have encouraged more students who did not have the required entry qualifications. Second, during the period of analysis, the overall entry grades went up by one grade each year. Such a dramatic rise was probably the reason for the slightly elevated numbers.

A Late Upper Aurignacian Station in North Lincolnshire

1932 ◽  
Vol 6 (4) ◽  
pp. 335-339
Author(s):  
A. Leslie Armstrong
Keyword(s):  
Upper Palaeolithic ◽  
Research Committee ◽  
Distinctive Character ◽  
Rock Shelter ◽  
English Expression ◽  
Gradual Development ◽  
The Subject ◽  
University Of Bristol ◽  
The University ◽  
First Time

The site forming the subject of this communication is an open-air station of Upper Palæolithic date, situated near the northern extremity of the Lincolnshire Cliff range, and previously unrecorded. The cultural horizon of the site closely corresponds with that of the upper levels of the rock-shelter known as ‘Mother Grundy's Parlour,’ Creswell Crags, Derbyshire, excavated by the writer in 1924, under the auspices of the British Association Research Committee for the Exploration of Caves in Derbyshire. Those excavations revealed, for the first time, the gradual development of our English phase of the Upper Aurignacian, and established the fact that this was of a distinctive character, and had been evolved practically free from Magdalenian influences. Excavations in the Mendip caves by the University of Bristol Spelæological Society, and elsewhere, have since confirmed these conclusions; and it is now recognised tlhat the culture is essentially an English expression of Upper Aurignacian, which is typical of the Upper Palæolithic in this country.

‘This Whole Project Has Given Me Focus, Hope and Positivity’: The Co Presentation of Findings

2017 ◽  
Author(s):  
Rachael Kiddey
Keyword(s):  
Cultural Heritage ◽  
Historical Archaeology ◽  
Public Archaeology ◽  
Contemporary Archaeology ◽  
Public Meetings ◽  
Heritage Studies ◽  
University Of Bristol ◽  
Medieval Archaeology ◽  
The University ◽  
Do So

I was explicitly clear with everyone who became involved in the Homeless Heritage project that the intention was to present our findings publically in a number of ways. We did this by co-publishing articles in popular magazines and peer-reviewed journals, speaking at public meetings and academic conferences, and through co-curating two interactive public exhibitions on the heritage of homelessness. It was important to spread the ways in which our findings were presented across a variety of platforms so that our results reached diverse audiences; for example, John Schofield, my homeless colleagues, and I published co-authored articles in The Big Issue, and in British Archaeology, in the hope that our work might reach people outside academia. That said, we were equally keen to demonstrate that the Homeless Heritage project was just as valid as archaeological investigations into any other marginalized culture or period so we also published co-authored peer-reviewed papers in Public Archaeology, Post-Medieval Archaeology, and created, in collaboration with artist Mats Brate, a comic based on fieldwork for the Journal of Contemporary Archaeology. Further to this, various book chapters were co-produced for academic books,6 and I have since published a paper for the International Journal of Heritage Studies, which focused on how cultural heritage methodologies can function as tools for empowerment. I encouraged my homeless colleagues to co-present papers at a variety of conferences and public talks. Jane, Danny, Deano, and Whistler co-presented a paper entitled ‘Punks and Drunks: Counter Mapping Homeless Heritage’ at the conference of the Theoretical Archaeology Group (TAG) at the University of Bristol in 2010, while Andrew, Jane, Dan, and Mark co-presented a paper called ‘Stories from the Street: Contemporary Homelessness as Heritage’ at the Postgraduate Conference in Historical Archaeology at the University of Leicester Centre for Historical Archaeology in 2011. To me, it was essential that those homeless colleagues who wanted to remain involved with the project once fieldwork had been completed were given real opportunities to do so.

Other Methods for Carbocyclic Construction: The Porco Synthesis of (-)-Hyperibone K

2013 ◽  
Author(s):  
Douglass F. Taber
Keyword(s):  
Oxidative Cyclization ◽  
Florida State University ◽  
State University ◽  
Colorado State University ◽  
Intramolecular Alkylation ◽  
University Of Wisconsin ◽  
Tokyo Institute ◽  
Institute Of Technology ◽  
University Of Bristol ◽  
The University

Varinder K. Aggarwal of the University of Bristol described (Angew. Chem. Int. Ed. 2010, 49, 6673) the conversion of the Sharpless-derived epoxide 1 into the cyclopropane 2. Christopher D. Bray of Queen Mary University of London established (Chem. Commun. 2010, 46, 5867) that the related conversion of 3 to 5 proceeded with high diastereocontrol. Javier Read de Alaniz of the University of California, Santa Barbara, extended (Angew. Chem. Int. Ed. 2010, 49, 9484) the Piancatelli rearrangement of a furyl carbinol 6 to allow inclusion of an amine 7, to give 8. Issa Yavari of Tarbiat Modares University described (Synlett 2010, 2293) the dimerization of 9 with an amine to give 10. Jeremy E. Wulff of the University of Victoria condensed (J. Org. Chem. 2010, 75, 6312) the dienone 11 with the commercial butadiene sulfone 12 to give the highly substituted cyclopentane 13. Robert M. Williams of Colorado State University showed (Tetrahedron Lett. 2010, 51, 6557) that the condensation of 14 with formaldehyde delivered the cyclopentanone 15 with high diastereocontrol. D. Srinivasa Reddy of Advinus Therapeutics devised (Tetrahedron Lett. 2010, 51, 5291) conditions for the tandem conjugate addition/intramolecular alkylation conversion of 16 to 17. Marie E. Krafft of Florida State University reported (Synlett 2010, 2583) a related intramolecular alkylation protocol. Takao Ikariya of the Tokyo Institute of Technology effected (J. Am. Chem. Soc. 2010, 132, 11414) the enantioselective Ru-mediated hydrogenation of bicyclic imides such as 18. This transformation worked equally well for three-, four-, five-, six-, and seven-membered rings. Stefan France of the Georgia Institute of Technology developed (Org. Lett. 2010, 12, 5684) a catalytic protocol for the homo-Nazarov rearrangement of the doubly activated cyclopropane 20 to the cyclohexanone 21. Richard P. Hsung of the University of Wisconsin effected (Org. Lett. 2010, 12, 5768) the highly diastereoselective rearrangement of the triene 22 to the cyclohexadiene 23. Strategies for polycyclic construction are also important. Sylvain Canesi of the Université de Québec devised (Org. Lett. 2010, 12, 4368) the oxidative cyclization of 24 to 25.

Enantioselective Construction of Alkylated Stereogenic Centers

2013 ◽  
Author(s):  
Douglass F. Taber
Keyword(s):  
Phase Transfer ◽  
Enantioselective Hydrogenation ◽  
Gel Chromatography ◽  
Quaternary Centers ◽  
University Of Oxford ◽  
University Of Edinburgh ◽  
Enantioselective Alkylation ◽  
Silica Gel Chromatography ◽  
University Of Bristol ◽  
The University

Xiang-Ping Hu and Zhuo Zheng of the Dalian Institute of Chemical Physics developed (Organic Lett. 2009, 11, 3226; J. Org. Chem. 2009, 74, 9191) a family of Rh catalysts for the enantioselective hydrogenation of allylic phosphonates such as 1. Hon Wai Lam of the University of Edinburgh established (J. Am. Chem. Soc. 2009, 131, 10386) that an alkenyl heterocycle 3 could be reduced with high ee. The product 4 could be hydrolyzed to the carboxylic acid. Ken Tanaka of the Tokyo University of Agriculture and Technology showed (J. Am. Chem. Soc. 2009, 131, 12552) that an isopropenyl amide 6 could be hydroacylated with high ee. Gregory C. Fu of MIT observed (J. Am. Chem. Soc. 2009, 131, 14231) that nitromethane 9 could be added to the allenyl amide 8 to give 10, the product of γ-bond formation. Robert K. Boeckman Jr. of the University of Rochester devised (Organic Lett. 2009, 11, 4544) what appears to be a general protocol for the construction of alkylated ternary and quaternary centers: enantioselective hydroxymethylation of an aldehyde 11. In another approach to the construction of alkylated quaternary centers, Varinder K. Aggarwal of the University of Bristol demonstrated (Angew. Chem. Int. Ed. 2009, 48, 6289) that an enantiomerically enriched trifluoroborate salt 14 could be added to an aromatic aldehyde 15 with retention of absolute configuration. The salt 14 was prepared from the corresponding high ee secondary benzyl alcohol. Weinreb amides are versatile precursors to a variety of functional groups. Stephen G. Davies of the University of Oxford devised (Organic Lett. 2009, 11, 3254) a chiral Weinreb amide equivalent 17 that could be alkylated with high de. The minor diastereomer from the alkylation was readily separable by silica gel chromatography. Keiji Maruoka of Kyoto University established (Angew. Chem. Int. Ed. 2009, 48, 5014) that a chiral phase transfer catalyst was effective for the enantioselective alkylation of the alkynyl ester 19. Emmanuel Riguet of the Université de Reims Champagne-Ardenne developed (Tetrahedron Lett. 2009, 50, 4283) an improved catalyst for the enantioselective addition of malonate 22 to cyclohexenone 21.

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