Tetrahedron Letters p. 3571 - 3574 (1994)
Update date:2022-08-04
Topics:
Kiso, Yoshiaki
Fukui, Toshio
Tanaka, Shigeki
Kimura, Tooru
Akaji, Kenichi
A new reductive acidolysis final deprotection strategy in solid phase peptide synthesis was developed using a new safety-catch linker; this new strategy was based on a two-dimensional protection scheme employing acid-labile temporary and acid-stable but reductive acidolysiscleavable semipermanent protecting groups.
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Doi:10.1021/ja01171a508
(1949)Doi:10.1021/jm980137o
(1998)Doi:10.1007/BF00954226
(1986)Doi:10.1021/jo01084a018
(1959)Doi:10.1039/c29690001229
(1969)Doi:10.1016/S0040-4020(97)00036-7
(1997)
