Authors:
Bahbouhi, B
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Chiva, C
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Albericio, F
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Seidah, NG
Bahraoui, E
Citation: B. Bahbouhi et al., Inhibition of HIV-2(ROD) replication in a lymphoblastoid cell line by the alpha 1-antitrypsin Portland variant (alpha 1-PDX) and the decRVKRcmk peptide: comparison with HIV-1(LAI), MICROBES IN, 3(13), 2001, pp. 1073-1084
Citation: W. Van Den Nest et al., Cu(OBt)(2) and Cu(OAt)(2), copper(II)-based racemization suppressors readyfor use in fully automated solid-phase peptide synthesis, J PEPT SCI, 7(3), 2001, pp. 115-120
Authors:
Royo, M
Van den Nest, W
del Fresno, M
Frieden, A
Yahalom, D
Rosenblatt, M
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Albericio, F
Citation: M. Royo et al., Solid-phase syntheses of constrained RGD scaffolds and their binding to the alpha(v)beta(3) integrin receptor, TETRAHEDR L, 42(42), 2001, pp. 7387-7391
Authors:
Fernandez-Forner, D
Casals, G
Navarro, E
Ryder, H
Albericio, F
Citation: D. Fernandez-forner et al., Solid-phase synthesis of 4-aminopiperidine analogues using the Alloc protecting group: an investigation of Alloc removal from secondary amines, TETRAHEDR L, 42(27), 2001, pp. 4471-4474
Authors:
Albericio, F
Cruz, M
Debethune, L
Eritja, R
Giralt, E
Grandas, A
Marchan, V
Pastor, JJ
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Royo, M
Citation: F. Albericio et al., An improved synthesis of N-[(9-hydroxymethyl)-2-fluorenyl]succinamic acid (HMFS), a versatile handle for the solid-phase synthesis of biomolecules, SYN COMMUN, 31(2), 2001, pp. 225-232
Authors:
Carreno, C
Mendez, ME
Kim, YD
Kim, HJ
Kates, SA
Andreu, D
Albericio, F
Citation: C. Carreno et al., Nsc and Fmoc N-alpha-amino protection for solid-phase peptide synthesis: aparallel study, J PEPT RES, 56(2), 2000, pp. 63-69
Citation: M. Pons et al., Disulfide bonded cyclic peptide dimers and trimers: An easy entry to high symmetry peptide frameworks, SYNLETT, (2), 2000, pp. 172-181
Authors:
Rabanal, F
Pastor, JJ
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Giralt, E
Citation: F. Rabanal et al., Synthesis of aspartimide-free protected peptides on base-labile functionalized resins, TETRAHEDR L, 41(42), 2000, pp. 8093-8096
Authors:
Alsina, J
Yokum, TS
Albericio, F
Barany, G
Citation: J. Alsina et al., A modified Backbone Amide Linker (BAL) solid-phase peptide synthesis strategy accommodating prolyl, N-alkylamino acyl, or histidyl derivatives at theC-terminus, TETRAHEDR L, 41(38), 2000, pp. 7277-7280
Citation: F. Albericio, Orthogonal protecting groups for N alpha-amino and C-terminal carboxyl functions in solid-phase peptide synthesis, BIOPOLYMERS, 55(2), 2000, pp. 123-139