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Rick L. Danheiser

Rick L. Danheiser 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 Rick L. Danheiser rather than just read about it. In short: Rick L. Danheiser is an American organic chemist and is the Arthur C.

Rick L. Danheiser — main illustration
Rick L. Danheiser — illustration

Key takeaways

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

Reference excerpt

Rick L. Danheiser is an American organic chemist and is the Arthur C. Cope Professor of Chemistry at the Massachusetts Institute of Technology and chair of the MIT faculty. His research involves the invention of new methods for the synthesis of complex organic compounds. Danheiser is known for the Danheiser annulation and Danheiser benzannulation reactions.

Education Danheiser was born in New York and received his B.A. in 1972 at Columbia College. While working as an undergraduate under the direction of Gilbert Stork, Danheiser developed a method for the regiospecific alkylation of beta-diketone enol ethers (the "Stork-Danheiser Alkylation"). and employed it in a total synthesis of the spiro sesquiterpene beta-vetivone. Danheiser received his Ph.D. at Harvard University in 1978. His doctoral research (under the direction of E. J. Corey) involved the first total synthesis of the diterpene plant growth hormone gibberellic acid.

Research Danheiser's research has focused on the development of new strategies for the synthesis of complex molecules and their application in the total synthesis of natural products. Synthetic methods invented in his laboratory include highly stereoselective [4 + 1] cyclopentene annulations based on oxyanion and carbanion-accelerated vinylcyclopropane rearrangements; the application of organosilanes (e.g., allenylsilanes, propargylsilanes, and allylsilanes) in a general [3 + 2] annulation strategy for the synthesis of five-membered carbocycles and heterocycles (the "Danheiser Annulation"); benzannulation strategies based on pericyclic transformations of vinylketenes (“Danheiser benzannulation”); methods for the synthesis of aromatic and dihydroaromatic compounds based on cycloadditions of highly unsaturated conjugated molecules such as conjugated 1,3-enynes; and formal [2 + 2 + 2] cycloadditions based on propargylic ene reaction/Diels-Alder cycloaddition cascades. Natural products synthesized in his laboratory at MIT include the neurotoxic alkaloids anatoxin a and quinolizidine 217A, the immunosuppressant agent mycophenolic acid the antitumor agent ascochlorin and a number of diterpene quinones derived from the Chinese traditional medicine Dan Shen.

Notable research awards Danheiser was awarded the Cope Scholar Award of the American Chemical Society in 1995. He is a Fellow of the American Chemical Society.

Teaching and service Danheiser has a particular interest in reproducibility in scientific research. He has been the editor-in-chief of the journal Organic Syntheses and a member of the board of directors of the Organic Syntheses corporation since 2004. Organic Syntheses has the unusual feature that all data and experiments reported in articles must be confirmed in the laboratory of a member of the editorial board prior to publication. Danheiser has a longstanding interest in laboratory safety and at MIT he has served as the chair of several committees including the MIT Chemistry Department EHS Committee which was recognized in 1991 as the first recipient of the American Chemical Society Division of Chemical Safety national award for "best university safety program". Danheiser also served on the National Research Council Committee on Prudent Practices for the Handling, Storage and Disposal of Chemicals in Laboratories, chairing the Subcommittee on Assessing Chemical Hazards. At MIT, Danheiser's educational contributions have been recognized with a MacVicar Faculty Fellowship, the School of Science Prize for Excellence in Undergraduate Teaching, the MIT Graduate Student Council Teaching Award, and the School of Science Prize for Graduate Education.

References

Illustrations

Rick L. Danheiser illustration

Worked examples

Example 1 — a first encounter with Rick L. Danheiser

Start with the simplest possible case. Write down what Rick L. Danheiser 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 Rick L. Danheiser 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 Rick L. Danheiser 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 Rick L. Danheiser

In research
Rick L. Danheiser 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 Rick L. Danheiser 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
Rick L. Danheiser is common in secondary-school and first-year university syllabi. It links to neighbouring topics 1951 births, 20th-century American chemists, American academic journal editors, so understanding it makes those chapters shorter.
In everyday life
Look for Rick L. Danheiser 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 Rick L. Danheiser in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Rick L. Danheiser 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 Rick L. Danheiser out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Rick L. Danheiser in simple terms?

Rick L. Danheiser is an American organic chemist and is the Arthur C.

Why does Rick L. Danheiser 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 Rick L. Danheiser?

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 Rick L. Danheiser.

Tags

  • 1951 births
  • 20th-century American chemists
  • American academic journal editors
  • American organic chemists
  • Columbia College, Columbia University alumni
  • Fellows of the American Academy of Arts and Sciences
  • Fellows of the American Chemical Society
  • Harvard University alumni
  • Living people
  • MIT School of Science faculty
  • Sloan Research Fellows

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