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Synthesis at the molecular frontier

Author

Listed:
  • Paul A. Wender

    (by courtesy, Stanford University, 333 Campus Drive, Stanford, California 94305-5080, USA. wenderp@stanford.edu)

  • Benjamin L. Miller

    (Benjamin L. Miller is in the School of Medicine and Dentistry, University of Rochester, 601 Elmwood Avenue, Box 697, Rochester, New York 14642, USA. Benjamin_miller@urmc.rochester.edu)

Abstract

Driven by remarkable advances in the understanding of structure and reaction mechanisms, organic synthesis will be increasingly directed to producing bioinspired and newly designed molecules.

Suggested Citation

  • Paul A. Wender & Benjamin L. Miller, 2009. "Synthesis at the molecular frontier," Nature, Nature, vol. 460(7252), pages 197-201, July.
    • Handle: RePEc:nat:nature:v:460:y:2009:i:7252:d:10.1038_460197a
    DOI: 10.1038/460197a
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    Cited by:

    1. Joel Häfliger & Louise Ruyet & Nico Stübke & Constantin G. Daniliuc & Ryan Gilmour, 2023. "Integrating I(I)/I(III) catalysis in reaction cascade design enables the synthesis of gem-difluorinated tetralins from cyclobutanols," Nature Communications, Nature, vol. 14(1), pages 1-8, December.
    2. Stefan Wiesler & Goh Sennari & Mihai V. Popescu & Kristen E. Gardner & Kazuhiro Aida & Robert S. Paton & Richmond Sarpong, 2024. "Late-stage benzenoid-to-troponoid skeletal modification of the cephalotanes exemplified by the total synthesis of harringtonolide," Nature Communications, Nature, vol. 15(1), pages 1-8, December.

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