(Q58036260)

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Hypersensitive acid-labile (HAL) tris(alkoxy)benzyl ester anchoring for solid-phase synthesis of protected peptide segments

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Hypersensitive acid-labile (HAL) tris(alkoxy)benzyl ester anchoring for solid-phase synthesis of protected peptide segments (English)

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Fernando Albericio

1

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author name string

George Barany

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2

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publication date

February 1991

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published in

Tetrahedron Letters

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volume

32

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issue

8

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page(s)

1015-1018

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cites work

Solid-phase peptide synthesis: a silver anniversary report.

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Synthetic peptides VH(27-68) and VH(16-68) of the myeloma immunoglobulin M603 heavy chain and their association with the natural light chain to form an antigen binding site

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7 January 2021

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Peptide and protein synthesis by segment synthesis-condensation.

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https://api.crossref.org/works/10.1016%2FS0040-4039%2800%2974475-3

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7 January 2021

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Comparative study of supports for solid-phase coupling of protected-peptide segments

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7 January 2021

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Convergent solid phase peptide synthesis. VII. Good yields in the coupling of protected segments on a solid support

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Orthogonal solid-phase synthesis of human gastrin-I under mild conditions

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

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An acid-labile anchoring linkage for solid-phase synthesis of C-terminal peptide amides under mild conditions

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Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions

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7 January 2021

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DOI

10.1016/S0040-4039(00)74475-3

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(Q58036260)

Hypersensitive acid-labile (HAL) tris(alkoxy)benzyl ester anchoring for solid-phase synthesis of protected peptide segments

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