- Tytuł:
-
Metody syntezy pochodnych organicznych zawierających wiązanie potrójne węgiel-węgiel
Methods for the synthesis of organic derivatives containing the triple bond carbon-carbon - Autorzy:
-
Bylińska, I.
Guzow, K. - Powiązania:
- https://bibliotekanauki.pl/articles/171636.pdf
- Data publikacji:
- 2012
- Wydawca:
- Polskie Towarzystwo Chemiczne
- Tematy:
-
wiązanie potrójne
acetylen
synteza
homosprzęganie
heterosprzęganie
reakcja Glasera
reakcja Haya
reakcja Cadiota-Chodkiewicza
reakcja Sonogashiry-Hagihary
triple bond
acetylene
synthesis
homocoupling
heterocoupling
Glaser reaction
Hay reaction
Cadiot-Chodkiewicz reaction
Sonogashira-Hagihara reaction - Opis:
- Compounds containing triple bonds are lately in the centre of interest of many research groups. This is mainly connected with their usefulness as substrates to obtain complex compounds with various applications in different areas of science, industry and medicine [1–5]. Because of that many researchers are interested in methods of synthesis of such compounds. As the demand for derivatives with triple bonds is quite big and the one universal method of synthesis does not exist, the new ones are developed or these already known are improved. To enable choosing the best method for synthesis of acetylene derivatives, this review is presented. The oldest methods based on elimination reaction are mentioned [6–9], whereas those enabling incorporation of acetylene unit into more complicated compounds are described more thoroughly [10–92]. The latter methods based on homo- or heterocoupling lead to symmetrical [10–25] and unsymmetrical acetylene and bisacetylene derivatives [26–92]. The most popular reactions such as Glaser reaction (Scheme 1) [10–12], Cadiot-Chodkiewicz reaction (Schemes 11 and 12) [26–49], Hay reaction (Scheme 13) [13, 14] as well as Sonogashira-Hagihara reaction [50–69] and their modifications (Tab. 3) [57] are described. Moreover, the influence of main parameters such as type of substrate used, ratio of reagents, catalyst, base, solvent, reaction time and temperature on the reaction yield is presented (Tabs 1–4) [14, 18, 23, 25, 50–58, 69–78].
- Źródło:
-
Wiadomości Chemiczne; 2012, 66, 9-10; 935-961
0043-5104
2300-0295 - Pojawia się w:
- Wiadomości Chemiczne
- Dostawca treści:
- Biblioteka Nauki
Artykuł