Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5224437 | Tetrahedron | 2009 | 6 Pages |
Abstract
We herein describe an in-depth screening and systematic comparison of five classical silyl alkyne protective groups, to evaluate their potential in the context of multiple successive copper (I)-catalyzed alkyne-azide cycloadditions (CuAAC). We confirm the relative sensitivity of TMS, especially under CuAAC conditions. The relative robustness of its higher analogues, and the discovery of mild silver-catalyzed deprotection conditions selective for TES compared to DPS or TIPS allowed us to design a strategy allowing three successive CuAAC on a single scaffold, as we have illustrated by the synthesis of a tris-triazolo model compound.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ibai E. Valverde, Agnès F. Delmas, Vincent Aucagne,