Libraries of 2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-2-amine derivatives via a multicomponent assembly process/1,3-dipolar cycloaddition strategy.

ACS Comb Sci

Department of Chemistry and Biochemistry, The Texas Institute for Drug and Diagnostic Development, The University of Texas, Austin, 78712, United States.

Published: January 2012

AI Article Synopsis

  • A new method combining Mannich-type multicomponent assembly with 1,3-dipolar cycloaddition has been created to quickly and effectively build a specific chemical structure known as tetrahydroisoquinoline fused isoxazolidine.
  • This newly formed structure can be further modified using established techniques to create a wide variety of chemical compounds.
  • The result is a diverse library of 70 different novel derivatives that belong to a specific category of compounds known as hexahydro-1H-pyrido[2,1-a]isoquinoline-2-amines.

Article Abstract

A Mannich-type multicomponent assembly process/1,3-dipolar cycloaddition strategy has been developed for the rapid and efficient construction of a parent tetrahydroisoquinoline fused isoxazolidine scaffold, which was subsequently functionalized using well-established protocols to access a diverse 70-membered library of novel 2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinoline-2-amine derivatives.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253940PMC
http://dx.doi.org/10.1021/co2001636DOI Listing

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