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Aromatic Helicenes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F21%3A00541160" target="_blank" >RIV/61388963:_____/21:00541160 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1201/9780429347290-4" target="_blank" >https://doi.org/10.1201/9780429347290-4</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1201/9780429347290-4" target="_blank" >10.1201/9780429347290-4</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Aromatic Helicenes

  • Original language description

    The point-to-helical chirality transfer utilizing a traceless chiral auxiliary features a remarkable independence from the diverse structural perturbations allowing for the preparation of both parent and functionalized fully aromatic helicenes in enantiomer ratios of >99:<1. Although there is still a way to go in order to develop a practical and general asymmetric synthesis of enantiopure helicenes, the recent achievements indicate that a solution to this problem present since the birth of helicene chemistry in 1956 is possible. Importantly, various synthetic methodologies were published to transform nonracemic biaryl precursors into nonracemic helicenes, thus demonstrating an excellent relay of stereochemical information when transforming axial chirality into helicity. The first promising attempts at this were already reported, and therefore, there are prospects to develop a general, practical and short catalytic asymmetric synthesis of enantiopure helicenes. Derivatives of nonracemic helicenes were found to respond reversibly to external stimuli constituting thus intriguing chiroptical switches.

  • Czech name

  • Czech description

Classification

  • Type

    C - Chapter in a specialist book

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GA16-08327S" target="_blank" >GA16-08327S: Chiral organic-inorganic hybrid materials and their use in nanoscience</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Book/collection name

    21st Century Nanoscience - A Handbook

  • ISBN

    978-0-8153-5528-1

  • Number of pages of the result

    29

  • Pages from-to

    "„4"-"1“-„4-29“"

  • Number of pages of the book

    484

  • Publisher name

    CRC Press

  • Place of publication

    Boca Raton

  • UT code for WoS chapter