Matches in SemOpenAlex for { <https://semopenalex.org/work/W2989711305> ?p ?o ?g. }
- W2989711305 endingPage "56" @default.
- W2989711305 startingPage "52" @default.
- W2989711305 abstract "We report herein that the Ir and Cu I bis‐metal catalyzed reductive alkynylation of amides, a method that we developed previously, can be extended to 6‐, 7‐, and 8‐membered lactams. The catalytic reductive alkynylation of 6‐methyl‐2‐piperidinones and its 3‐benzyloxy derivative proceeded with 2.3:1 to 7:1 2,6‐ trans/cis diastereoselectivities. The resulting piperidines were converted into alkaloids (±)‐solenopsin, (±)‐solenopsin A, and (+)‐julifloridine all in only one step. This two‐step approach to the alkaloids is much shorter and much efficient than the conventional multistep methods." @default.
- W2989711305 created "2019-12-05" @default.
- W2989711305 creator A5000035170 @default.
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- W2989711305 creator A5015948426 @default.
- W2989711305 creator A5021141602 @default.
- W2989711305 creator A5048553281 @default.
- W2989711305 date "2019-12-20" @default.
- W2989711305 modified "2023-10-01" @default.
- W2989711305 title "Two-Step Catalytic Transformation of <i>N</i> -Benzyllactams to Alkaloids (±)-Solenopsin, (±)-Solenopsin A, and (+)-Julifloridine" @default.
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