(Q58036158)

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Solid-phase synthesis of peptides using allylic anchoring groups 2. Palladium-catalysed cleavage of Fmoc-protected peptides

scholarly article by Paul Lloyd-Williams et al published June 1994 in Tetrahedron Letters

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Solid-phase synthesis of peptides using allylic anchoring groups 2. Palladium-catalysed cleavage of Fmoc-protected peptides (English)

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Ernest Giralt i Lledó

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5

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Ernest Giralt

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Paul Lloyd-Williams

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Paul Lloyd-Williams

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1

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Fernando Albericio

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Fernando Albericio

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4

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Ahmed Merzouk

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2

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François Guibé

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3

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publication date

June 1994

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published in

Tetrahedron Letters

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volume

35

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issue

25

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page(s)

4437-4440

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Convergent solid-phase peptide synthesis

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A new amino protecting group removable by reduction. Chemistry of the dithiasuccinoyl (Dts) function

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Automated Allyl Cleavage for Continuous-Flow Synthesis of Cyclic and Branched Peptides

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Convergent solid-phase peptide synthesis. XI. Synthesis and purification of protected peptide segments spanning the entire sequence of the uteroglobin monomer using the photolabile nbb-resin

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Use of BOP reagent for the suppression of diketopiperazine formation in boc/bzl solid-phase peptide synthesis

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10.1016/S0040-4039(00)73378-8

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(Q58036158)

Solid-phase synthesis of peptides using allylic anchoring groups 2. Palladium-catalysed cleavage of Fmoc-protected peptides

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