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Marine Drugs|May 24, 2013
"Head-to-side-chain" cyclodepsipeptides of marine originMarta Pelay-Gimeno, Judit Tulla-Puche, Fernando AlbericioNature Protocols|September 23, 2016
Synthesis of complex head-to-side-chain cyclodepsipeptidesMarta Pelay-Gimeno, Fernando Albericio, Judit Tulla-PucheJournal of Medicinal Chemistry|November 21, 2013
Rescuing biological activity from synthetic phakellistatin 19Marta Pelay-Gimeno, Alessandra Meli, Judit Tulla-Puche, et al.Organic Letters|December 24, 2011
Solid-phase synthesis of NMe-IB-01212, a highly N-methylated cyclic peptideEleonora Marcucci, Judit Tulla-Puche, Fernando AlbericioCurrent Drug Delivery|May 30, 2012
Polymers and drug delivery systemsGemma Vilar, Judit Tulla-Puche, Fernando AlbericioACS Combinatorial Science|April 12, 2013
Handles for Fmoc solid-phase synthesis of protected peptidesMiriam Góngora-Benítez, Judit Tulla-Puche, Fernando AlbericioFuture Medicinal Chemistry|March 8, 2013
Constella™(EU)-Linzess™(USA): the last milestone in the long journey of the peptide linaclotide and its implications for the future of peptide drugsMiriam Góngora-Benítez, Judit Tulla-Puche, Fernando AlbericioChemical Society Reviews|November 28, 2015
The road to the synthesis of "difficult peptides"Marta Paradís-Bas, Judit Tulla-Puche, Fernando AlbericioOrganic Letters|December 30, 2014
Semipermanent C-terminal carboxylic acid protecting group: application to solubilizing peptides and fragment condensationMarta Paradís-Bas, Judit Tulla-Puche, Fernando AlbericioChemistry (Weinheim an Der Bergstrasse, Germany)|October 4, 2014
2-Methoxy-4-methylsulfinylbenzyl: a backbone amide safety-catch protecting group for the synthesis and purification of difficult peptide sequencesMarta Paradís-Bas, Judit Tulla-Puche, Fernando AlbericioPageof 52