Matches in SemOpenAlex for { <https://semopenalex.org/work/W2913247436> ?p ?o ?g. }
- W2913247436 endingPage "3406" @default.
- W2913247436 startingPage "3402" @default.
- W2913247436 abstract "Abstract The highly enantioselective addition of terminal ynamides to a variety of isatins, catalyzed by a bisoxazolidine copper complex under mild, base‐free reaction conditions, is described. The reaction is broad in scope, scalable, applicable to unprotected isatins, and provides efficient access to 3‐hydroxyoxindoles carrying a tetrasubstituted chiral center with excellent yields and enantioselectivities. Synthetically versatile, multifunctional 3‐hydroxyindolinones are obtained by hydration, partial hydrogenation, or hydroxyacyloxylation of the ynamide moiety at room temperature and exhaustive hydrogenation followed by reductive detosylation and spontaneous cyclization affords cinchonamidine alkaloids." @default.
- W2913247436 created "2019-02-21" @default.
- W2913247436 creator A5036327556 @default.
- W2913247436 creator A5081721254 @default.
- W2913247436 date "2019-02-14" @default.
- W2913247436 modified "2023-10-17" @default.
- W2913247436 title "Catalytic Enantioselective Ynamide Additions to Isatins: Concise Access to Oxindole Alkaloids" @default.
- W2913247436 cites W1881475433 @default.
- W2913247436 cites W1963814845 @default.
- W2913247436 cites W1964007719 @default.
- W2913247436 cites W1974410330 @default.
- W2913247436 cites W1979194753 @default.
- W2913247436 cites W1985515616 @default.
- W2913247436 cites W1989716825 @default.
- W2913247436 cites W2000630300 @default.
- W2913247436 cites W2005335584 @default.
- W2913247436 cites W2005404928 @default.
- W2913247436 cites W2007265737 @default.
- W2913247436 cites W2007276881 @default.
- W2913247436 cites W2018164191 @default.
- W2913247436 cites W2022562953 @default.
- W2913247436 cites W2030336847 @default.
- W2913247436 cites W2042105273 @default.
- W2913247436 cites W2043049018 @default.
- W2913247436 cites W2052525126 @default.
- W2913247436 cites W2061154455 @default.
- W2913247436 cites W2063405275 @default.
- W2913247436 cites W2065868460 @default.
- W2913247436 cites W2066960454 @default.
- W2913247436 cites W2079877381 @default.
- W2913247436 cites W2083990575 @default.
- W2913247436 cites W2085490330 @default.
- W2913247436 cites W2086311749 @default.
- W2913247436 cites W2090636011 @default.
- W2913247436 cites W2105480157 @default.
- W2913247436 cites W2108610966 @default.
- W2913247436 cites W2117051429 @default.
- W2913247436 cites W2123793395 @default.
- W2913247436 cites W2125498527 @default.
- W2913247436 cites W2128028867 @default.
- W2913247436 cites W2128778636 @default.
- W2913247436 cites W2131717469 @default.
- W2913247436 cites W2132665169 @default.
- W2913247436 cites W2135180430 @default.
- W2913247436 cites W2138790951 @default.
- W2913247436 cites W2148972318 @default.
- W2913247436 cites W2149358861 @default.
- W2913247436 cites W2156815201 @default.
- W2913247436 cites W2162389885 @default.
- W2913247436 cites W2168300222 @default.
- W2913247436 cites W2168502620 @default.
- W2913247436 cites W2170755274 @default.
- W2913247436 cites W2252822894 @default.
- W2913247436 cites W2265307865 @default.
- W2913247436 cites W2279953105 @default.
- W2913247436 cites W2297369877 @default.
- W2913247436 cites W2345574398 @default.
- W2913247436 cites W2437690475 @default.
- W2913247436 cites W2461347989 @default.
- W2913247436 cites W2468754760 @default.
- W2913247436 cites W2521500813 @default.
- W2913247436 cites W2525732633 @default.
- W2913247436 cites W2563876488 @default.
- W2913247436 cites W2566931184 @default.
- W2913247436 cites W2567586155 @default.
- W2913247436 cites W2589915296 @default.
- W2913247436 cites W2737300577 @default.
- W2913247436 cites W2753823469 @default.
- W2913247436 cites W2757975890 @default.
- W2913247436 cites W2762339105 @default.
- W2913247436 cites W2763352924 @default.
- W2913247436 cites W2767244228 @default.
- W2913247436 cites W2779444628 @default.
- W2913247436 cites W2781313887 @default.
- W2913247436 cites W2784169609 @default.
- W2913247436 cites W2789454723 @default.
- W2913247436 cites W2789704257 @default.
- W2913247436 cites W2791997142 @default.
- W2913247436 cites W2794333752 @default.
- W2913247436 cites W2801822336 @default.
- W2913247436 cites W2811498769 @default.
- W2913247436 cites W2900088889 @default.
- W2913247436 cites W2951361128 @default.
- W2913247436 cites W2951912922 @default.
- W2913247436 cites W2952242072 @default.
- W2913247436 cites W2952523289 @default.
- W2913247436 cites W2953141525 @default.
- W2913247436 cites W3140980066 @default.
- W2913247436 cites W4229882201 @default.
- W2913247436 cites W4230019582 @default.
- W2913247436 cites W4231634730 @default.
- W2913247436 cites W4234216206 @default.
- W2913247436 cites W4234643618 @default.
- W2913247436 cites W4235729295 @default.
- W2913247436 cites W4236064320 @default.
- W2913247436 cites W4236998032 @default.
- W2913247436 cites W4237316769 @default.
- W2913247436 cites W4237540691 @default.