Title of article
Solid-phase synthesis of 4-aminopiperidine analogues using the Alloc protecting group: an investigation of Alloc removal from secondary amines
Author/Authors
Fern?ndez-Forner، نويسنده , , Dolors and Casals، نويسنده , , Gaspar and Navarro، نويسنده , , Elo??sa and Ryder، نويسنده , , Hamish and Albericio، نويسنده , , Fernando، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2001
Pages
4
From page
4471
To page
4474
Abstract
A useful method for Alloc removal from secondary amines on solid-phase has been optimised. The use of Me2NH·BH3 (40 equiv., 40 min) as scavenger of the allyl cations in a palladium-catalysed process with Pd[PPh3]4 leads to quantitative removal of the Alloc group without any allyl back alkylation. Other scavengers such as morpholine or PhSiH3 are clearly inferior. Furthermore, this study has highlighted differences in the reaction kinetics of the deprotection step between secondary and primary amines such as those from α-amino acids.
Keywords
Combinatorial chemistry , allyl protecting groups , Diversity , reductive amination
Journal title
Tetrahedron Letters
Serial Year
2001
Journal title
Tetrahedron Letters
Record number
1645570
Link To Document