Matches in SemOpenAlex for { <https://semopenalex.org/work/W3202670669> ?p ?o ?g. }
- W3202670669 endingPage "25142" @default.
- W3202670669 startingPage "25135" @default.
- W3202670669 abstract "Chiral tetrahydro-β-carboline (THβC) is not only a prevailing structural feature of many natural alkaloids but also a versatile synthetic precursor for a vast array of monoterpenoid indole alkaloids. Asymmetric synthesis of C1-alkynyl THβCs remains rarely explored and challenging. Herein, we describe the development of two complementary approaches for the catalytic asymmetric alkynylation of 3,4-dihydro-β-carbolinium ions with up to 96 % yield and 99 % ee. The utility of chiral C1-alkynyl THβCs was demonstrated by the collective total syntheses of seven indole alkaloids: harmicine, eburnamonine, desethyleburnamonine, larutensine, geissoschizol, geissochizine, and akuammicine." @default.
- W3202670669 created "2021-10-11" @default.
- W3202670669 creator A5032967725 @default.
- W3202670669 creator A5039677409 @default.
- W3202670669 creator A5042455393 @default.
- W3202670669 creator A5058714206 @default.
- W3202670669 date "2021-10-20" @default.
- W3202670669 modified "2023-10-16" @default.
- W3202670669 title "Catalytic Asymmetric Alkynylation of 3,4‐Dihydro‐β‐carbolinium Ions Enables Collective Total Syntheses of Indole Alkaloids" @default.
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