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Synthesis of Helicenes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F25%3A00619410" target="_blank" >RIV/61388963:_____/25:00619410 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1002/9783527845019.ch5" target="_blank" >https://doi.org/10.1002/9783527845019.ch5</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/9783527845019.ch5" target="_blank" >10.1002/9783527845019.ch5</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis of Helicenes

  • Original language description

    Advanced molecular nanocarbons have attracted considerable attention in chemistry, physics, and nanoscience and have stimulated extensive research on complex molecular systems rich in carbon and π-electrons. This class of compounds is structurally diverse and also comprises nanocarbons with broken mirror symmetry, such as helicenes and their congeners. The combination of delocalized π-electrons with the inherent chirality of scaffolds makes these molecules attractive for envisaged applications in various scientific fields. This chapter focuses on the description of methods for their preparation that have gained considerable popularity or are of general applicability, including the synthesis of enantiopure helicenes. Not only the photocyclodehydrogenation of stilbene-type precursors, multiple Scholl reaction, [2+2+2] cycloisomerization of alkynes, Diels-Alder cycloaddition, or hydroarylation of alkynes but also other methods of helicene synthesis are presented. In addition to the preparation of parent helicenes, their heteroanalogues or helicene-like compounds, the approach to advanced helicene architectures such as long helicenes, π-extended helicenes, multiple helicenes, helicenoid twistacenes, and helicene macrocycles is briefly described.

  • Czech name

  • Czech description

Classification

  • Type

    C - Chapter in a specialist book

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

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

Data specific for result type

  • Book/collection name

    Molecular Nanographenes: Synthesis, Properties, and Applications

  • ISBN

    978-3-527-35322-4

  • Number of pages of the result

    44

  • Pages from-to

    105-148

  • Number of pages of the book

    524

  • Publisher name

    Wiley

  • Place of publication

    Weinheim

  • UT code for WoS chapter