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John Buckingham (chemist)

John Buckingham (chemist) is a chemistry topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand John Buckingham (chemist) rather than just read about it. In short: John Buckingham (21 March 1943 – 28 August 2015) was a British chemist known for his authorship of several chemical dictionaries including the Dictionary of Natural Products. Education and career John Buckingham won a scholarship to Haberdashers’ Aske's Boys' School at the age of 11.

John Buckingham (chemist) — main illustration
John Buckingham (chemist) — illustration

Key takeaways

  • John Buckingham (chemist) belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect John Buckingham (chemist) to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of John Buckingham (chemist) from memory before moving on to harder problems.

Reference excerpt

John Buckingham (21 March 1943 – 28 August 2015) was a British chemist known for his authorship of several chemical dictionaries including the Dictionary of Natural Products.

Education and career John Buckingham won a scholarship to Haberdashers’ Aske's Boys' School at the age of 11. It was there that he discovered chemistry and chose to apply to the University of Southampton where he won a First Class Honours degree. He gained his D.Phil. from the University of Sussex. He became a lecturer in Chemistry in William Klyne’s department at Westfield College, University of London. Professor Klyne was writing a book on organic stereochemistry for Chapman & Hall and John’s expertise and attention to detail made him the ideal co-author. So the Atlas of Stereochemistry was published in 1974 to great reviews, with two subsequent volumes following a few years later. John’s skills were recognized by the managing director at Chapman & Hall, Richard Stileman, who then engaged him on a full-time basis to prepare a new edition of the Heilbron’s Dictionary of Organic Compounds (DOC). This was a multi-volume reference work which needed bringing into the modern world with significant amendments required for the fifth edition. John was pivotal in converting the DOC into a database, and this now forms the basis of the modern DOC and its related dictionaries. Once the DOC was published, John’s attention turned towards the chemistry of natural products such as alkaloids including strychnine and morphine, taxol. John had the foresight to anticipate the tremendous growth in natural products research and its relevance to the modern drug industry. His expertise with deciphering chemical literature and organising natural products by structure, coupled with his unflagging energy and enthusiasm, culminated in the publication of the Dictionary of Natural Products. This heralded a new phase of publishing with electronic products very much at the forefront. The CD ROM version of the Dictionary was published in 1991, two years before the book was published. It continues to be updated twice a year and John continued working on it full-time until the end. As Fiona Macdonald, the current editor of the Dictionary commented in a eulogy at his memorial service: "No other publication has ever achieved the breadth and depth of the Dictionary of Natural Products and today it is widely regarded as the benchmark in natural product information. John was very proud of its success and it truly is his life’s work and his legacy." Buckingham also wrote two books for the general reader which covered chemical subjects. These are Chasing the Molecule, about the development of Chemistry as a science and Bitter Nemesis, the story of strychnine's introduction to Europe, its adoption first as a medicine, and later as a poison. In Chapter 16, Bitter Nemesis, he opens with the First World War to lead into a retelling of "a plot, now widely forgotten, to assassinate Lloyd George and Arthur Henderson, Leader of the Labour Party and member of the War Cabinet". Before publication there were several history sources, newspaper and media reports pointing to the likelihood that the plot was a fabrication of the undercover agent who was kept out of the trial of Alice Wheeldon and her family, and that the trial was unsafe. John Buckingham is buried in Kensal Green Cemetery in London, United Kingdom.

Notable works Atlas of Stereochemistry: Absolute Configurations of Organic Molecules. (Springer 1974, ISBN 0412106302) Dictionary of Natural Products. (Chapman and Hall/CRC 1993, ISBN 9780412466205) Dictionary of Organic Compounds, Sixth Edition. (Chapman and Hall/CRC 1995, ISBN 9780849300073) Chasing the Molecule. (The History Press 2004, ISBN 0750933453) Bitter Nemesis: The Intimate History of Strychnine. (CRC Press 2007, ISBN 9781420053159) Dictionary of Alkaloids, Second Edition. (CRC Press 2010, ISBN 9781420077698)

References

Snatzke, G. (1975), Book Review: Atlas of Stereochemistry. Absolute Configurations of Organic Molecules. By W. Klyne and J. Buckingham. Angew. Chem. Int. Ed. Engl., 14: 441–444. doi:10.1002/anie.197504412

Illustrations

John Buckingham (chemist) illustration

Worked examples

Example 1 — a first encounter with John Buckingham (chemist)

Start with the simplest possible case. Write down what John Buckingham (chemist) claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to John Buckingham (chemist) before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about John Buckingham (chemist) ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of John Buckingham (chemist)

In research
John Buckingham (chemist) appears in chemistry research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses John Buckingham (chemist) in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
John Buckingham (chemist) is common in secondary-school and first-year university syllabi. It links to neighbouring topics 1943 births, 2015 deaths, British chemists, so understanding it makes those chapters shorter.
In everyday life
Look for John Buckingham (chemist) outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study John Buckingham (chemist) in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what John Buckingham (chemist) means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain John Buckingham (chemist) out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is John Buckingham (chemist) in simple terms?

John Buckingham (21 March 1943 – 28 August 2015) was a British chemist known for his authorship of several chemical dictionaries including the Dictionary of Natural Products. Education and career John Buckingham won a scholarship to Haberdashers’ Aske's Boys' School at the age of 11.

Why does John Buckingham (chemist) matter?

Because it connects several chemistry ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study John Buckingham (chemist)?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on John Buckingham (chemist).

Tags

  • 1943 births
  • 2015 deaths
  • British chemists
  • People educated at Haberdashers' Boys' School
  • Scientists from London

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