Microwave Heating in the Solid-Phase Synthesis ofN-Methylated Peptides: When Is Room Temperature Better?

Effect of Residual Water and Microwave Heating on the Half-Life of the Reagents and Reactive Intermediates in Peptide Synthesis

(2012) A. Pernille Tofteng et al.   CHEMISTRY-A EUROPEAN JOURNAL

Microwave heating in solid-phase peptide synthesis

(2011) Søren L. Pedersen et al.   CHEMICAL SOCIETY REVIEWS

Solid-Phase Synthesis of NMe-IB-01212, a Highly N-Methylated Cyclic Peptide

(2011) Eleonora Marcucci et al.   ORGANIC LETTERS

N-Methylated sst2 Selective Somatostatin Cyclic Peptide Analogue as a Potent Candidate for Treating Neurogenic Inflammation

(2011) Jayanta Chatterjee et al.   ACS Medicinal Chemistry Letters

MultipleN-Methylation of MT-II Backbone Amide Bonds Leads to Melanocortin Receptor Subtype hMC1R Selectivity: Pharmacological and Conformational Studies

(2010) Lucas Doedens et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Amino Acid-Protecting Groups

(2009) Albert Isidro-Llobet et al.   CHEMICAL REVIEWS

COMU: A Safer and More Effective Replacement for Benzotriazole-Based Uronium Coupling Reagents

(2009) Ayman El-Faham et al.   CHEMISTRY-A EUROPEAN JOURNAL

Oxyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based HOBt and HOAt with a Lower Risk of Explosion[1]

(2009) Ramon Subirós-Funosas et al.   CHEMISTRY-A EUROPEAN JOURNAL

Efficient Synthesis of Peptides by Extension at the N- and C-Terminii of Arginine

(2008) Alan R. Katritzky et al.   JOURNAL OF ORGANIC CHEMISTRY