Synthetic chemistry in water: applications to peptide synthesis and nitro-group reductions

[1]  T. Sheppard,et al.  Protecting‐Group‐Free Amidation of Amino Acids using Lewis Acid Catalysts , 2018, Chemistry.

[2]  J. Murray,et al.  Cyrene as a bio-based solvent for HATU mediated amide coupling. , 2018, Organic & biomolecular chemistry.

[3]  C. Bucher,et al.  N-Butylpyrrolidinone as Alternative Solvent for Solid-Phase Peptide Synthesis , 2018 .

[4]  F. Gallou,et al.  Carbonyl Iron Powder: A Reagent for Nitro Group Reductions under Aqueous Micellar Catalysis Conditions. , 2017, Organic letters.

[5]  J. Berthon,et al.  Tandem deprotection/coupling for peptide synthesis in water at room temperature , 2017 .

[6]  T. Sheppard,et al.  Borate esters: Simple catalysts for the sustainable synthesis of complex amides , 2017, Science Advances.

[7]  S. Lawrenson,et al.  The greening of peptide synthesis , 2017 .

[8]  B. Lipshutz When Does Organic Chemistry Follow Nature's Lead and "Make the Switch"? , 2017, The Journal of organic chemistry.

[9]  M. Benaglia,et al.  Recent Developments in the Reduction of Aromatic and Aliphatic Nitro Compounds to Amines , 2016 .

[10]  Jonas Boström,et al.  Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone? , 2016, Journal of medicinal chemistry.

[11]  S. Tilve,et al.  Advancement in methodologies for reduction of nitroarenes , 2015 .

[12]  F. Gallou,et al.  Amide and Peptide Bond Formation in Water at Room Temperature. , 2015, Organic letters.

[13]  Fernando Albericio,et al.  Peptide synthesis beyond DMF: THF and ACN as excellent and friendlier alternatives. , 2015, Organic & biomolecular chemistry.

[14]  J. Wade,et al.  Aqueous microwave-assisted solid-phase peptide synthesis using Fmoc strategy. III: Racemization studies and water-based synthesis of histidine-containing peptides , 2014, Amino Acids.

[15]  Jean Martínez,et al.  Environmentally benign peptide synthesis using liquid-assisted ball-milling: application to the synthesis of Leu-enkephalin , 2013 .

[16]  Jean Martínez,et al.  Mechanosynthesis of amides in the total absence of organic solvent from reaction to product recovery. , 2012, Chemical communications.

[17]  A. Sood,et al.  Steps Toward Green Peptide Synthesis , 2011 .

[18]  Jean Martínez,et al.  Solvent-free synthesis of peptides. , 2009, Angewandte Chemie.

[19]  K. Wehrstedt,et al.  Explosive properties of 1-hydroxybenzotriazoles. , 2005, Journal of hazardous materials.

[20]  M. Maeda,et al.  2-(4-Sulfophenylsulfonyl)ethoxycarbonyl group: a new water-soluble N-protecting group and its application to solid phase peptide synthesis in water , 2004 .

[21]  J. M. Lipton,et al.  Antiinflammatory influences of alpha-MSH molecules: central neurogenic and peripheral actions , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.