Comprehensive Heterocyclic Chemistry IV 2022
DOI: 10.1016/b978-0-12-409547-2.14894-2
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Bicyclic 5-6 Systems: Four Heteroatoms 3:1

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“…Similar to the Suzuki-Miyaura cross coupling, the Stille cross coupling has also found extensive application and versatility in transition metal-catalyzed reactions for the construction of a variety of conjugated polymers and organic compounds through the formation of C(sp 2 )-C(sp 2 ) bonds [90]. This reaction involves coupling between aryl stanners species with organic electrophiles such as aryl halide in the presence of palladium, Pd (0), as a catalyst (Scheme 11) [91,92]. The success and widespread use of this reaction is attributed to the mild reagents of organotin, which are well matched with a diverse number of functional groups [93,94].…”
Section: Stille Cross-coupling Reactionmentioning
confidence: 99%
“…Similar to the Suzuki-Miyaura cross coupling, the Stille cross coupling has also found extensive application and versatility in transition metal-catalyzed reactions for the construction of a variety of conjugated polymers and organic compounds through the formation of C(sp 2 )-C(sp 2 ) bonds [90]. This reaction involves coupling between aryl stanners species with organic electrophiles such as aryl halide in the presence of palladium, Pd (0), as a catalyst (Scheme 11) [91,92]. The success and widespread use of this reaction is attributed to the mild reagents of organotin, which are well matched with a diverse number of functional groups [93,94].…”
Section: Stille Cross-coupling Reactionmentioning
confidence: 99%