1985
DOI: 10.1002/chin.198538241
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ChemInform Abstract: PREPARATION AND REACTIONS OF 2‐ALKYNYL‐3‐CHLOROQUINOXALINES

Abstract: Durch Umsetzung der Chlorchinoxaline (I) mit entsprechenden Alkinen (II) erhält man die Kondensationsprodukte (III) bzw. (IV); aus den Hme‐Derivaten lassen sich mit trokkenem NaOH durch Abspaltung von Aceton die freien Alkine (V) gewinnen.

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“…However, we adopted a new synthetic strategy, wherein we chose to first prepare the tricyclic skeleton and then introduce a protected dithiolene moiety [39,40]. Starting from 2,3-dichloroquioxaline 12, the tricyclic molecule 13 was prepared in two steps according to a reported method [41]. The enol ether was hydrolyzed to the corresponding enol 14, which was functionalized by bromination to 15 and activated by triflation to give 16.…”
Section: Pyrazine Containing Ligandsmentioning
confidence: 99%
“…However, we adopted a new synthetic strategy, wherein we chose to first prepare the tricyclic skeleton and then introduce a protected dithiolene moiety [39,40]. Starting from 2,3-dichloroquioxaline 12, the tricyclic molecule 13 was prepared in two steps according to a reported method [41]. The enol ether was hydrolyzed to the corresponding enol 14, which was functionalized by bromination to 15 and activated by triflation to give 16.…”
Section: Pyrazine Containing Ligandsmentioning
confidence: 99%