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연사: 이화여자대학교, 장원준 교수님 일자: 10월 2일 목요일 오후5시부터~ 장소: 건국대학교 과학관201호
Nickel-Catalyzed Cross-Electrophile
Coupling for Enantioselective C(sp³)–C(sp²) and C(sp³)–C(sp) Bond Formation
초록:
Nickel-catalyzed cross-electrophile coupling (XEC) has emerged as
a powerful and versatile strategy for C–C bond formation, allowing the use of
readily available electrophiles while avoiding the need for pre-functionalized
organometallic nucleophiles. In this presentation, our recent developments in
Ni-catalyzed XEC will be discussed, focusing on two key transformations:
(1) the alkylation of alkynyl halides1
and (2) the enantioselective alkylation of aryl halides using unactivated alkyl
halides.2 Mechanistic studies have revealed that the alkylation of alkynyl
halides proceeds via an unexpected pathway, distinct from previously reported
XEC mechanisms, providing new
insights into Ni- catalyzed
XEC reactions. For the alkylation of aryl halides, a chiral nickel catalyst system was
employed to achieve
enantioselective
cross-electrophile coupling.
Furthermore, a unique
chain- walking strategy was developed to enable divergent functionalization
directly from alkyl halides, expanding the synthetic utility of XEC.
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