Title of article :
Synthesis of new diverse macrocycles from diol precursors
Author/Authors :
Charlotte M. Madsen، نويسنده , , Martin Hansen، نويسنده , , Marie V. Thrane، نويسنده , , Mads H. Clausen، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2010
Abstract :
The formation of a library of diverse macrocycles with different ring sizes from two easily accessible building blocks is presented. Reacting diol precursors with electrophilic reagents lead to 17-membered sulfites and 19-membered malonates in 34–79% yield. Double-reductive amination of dialdehyde analogs of the diol precursors leads to 15-membered amines in yields ranging from 9 to 60%, reflecting large differences in reactivity based on steric environment.
Keywords :
macrocyclization , Cyclic esters , Reductive amination , Diversity-oriented synthesis
Journal title :
Tetrahedron
Journal title :
Tetrahedron