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- W2208368370 abstract "Tetrasubstituted alkene-based 1,2,3,4-tetrahydroisoquinolines are synthesized via the formation of a cyclic carbopalladation complex followed by C–H bond activation of the sp2 carbon in arenes. This domino reaction proceeds with good selectivity and provides good yields of the products. The requisite starting materials are synthesized by copper(I) iodide catalyzed A3-coupling reactions." @default.
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- W2208368370 date "2015-09-24" @default.
- W2208368370 modified "2023-09-24" @default.
- W2208368370 title "ChemInform Abstract: Synthesis of 4-Alkylidene-Substituted 1,2,3,4-Tetrahydroisoquinolines via Palladium-Catalyzed Carbopalladation/C-H Activation of 2-Bromobenzyl-N-propargylamines." @default.
- W2208368370 cites W2950749463 @default.
- W2208368370 doi "https://doi.org/10.1002/chin.201541186" @default.
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