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  • SnCl2-catalyzed selective atom economic imino Diels-Alder reaction: synthesis of 2-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolines.

SnCl2-catalyzed selective atom economic imino Diels-Alder reaction: synthesis of 2-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolines.

The Journal of organic chemistry (2012-01-11)
Rajendran Suresh, Shanmugam Muthusubramanian, Rajendran Senthilkumaran, Govindaswamy Manickam
ZUSAMMENFASSUNG

The synthesis of 2-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolines by a SnCl(2)-catalyzed multicomponent reaction has been described. The reaction proceeds chemo- and regioselectively in an atom-economic way, generating a library of 24 quinoline derivatives.

MATERIALIEN
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Produktbeschreibung

Sigma-Aldrich
Zinn(II)-Chlorid, reagent grade, 98%
Sigma-Aldrich
Zinn(II)-chlorid Dihydrat, ACS reagent, 98%
Sigma-Aldrich
Zinn(II)-chlorid Dihydrat, reagent grade, 98%
Sigma-Aldrich
Zinn(II)-chlorid Dihydrat, ≥99.99% trace metals basis
Sigma-Aldrich
Zinn(II)-chlorid Dihydrat, ≥99.97% trace metals basis
Sigma-Aldrich
Zinn(II)-Chlorid, anhydrous, powder, ≥99.99% trace metals basis
Sigma-Aldrich
Zinn(II)-Chlorid, ≥99.99% trace metals basis
Supelco
Zinn(II)-chlorid Dihydrat, suitable for AAS