Daniel Riemer, Pradipbhai Hirapara, Shoubhik Das. Fmoc-OASUD: A new reagent for the preparation of Fmoc-amino acids free from impurities resulting from Lossen rearrangement. Facile one-pot synthesis of unsymmetrical ureas, carbamates, and thiocarbamates from Cbz-protected amines. Chemical Synthesis of Human Insulin-Like Peptide-6. Ana C. Mendes, Erkan T. Baran, Rui L. Reis, Helena S. Azevedo. Manashjyoti Konwar, Abdul Aziz Ali, Diganta Sarma. Carlo Diaferia, Nicole Balasco, Teresa Sibillano, Cinzia Giannini, Luigi Vitagliano, Giancarlo Morelli, Antonella Accardo. DOTA-tris(OPp ester) as a bifunctional prochelator for the preparation of DOTA–peptide conjugates. -Butoxycarbonyloxy)-5-norbornene-
An improved, scalable synthesis of bis-amino acids. P. chrysogenum
Boron Accumulation in Brain Tumor Cells through Boc-Protected Tryptophan as a Carrier for Boron Neutron Capture Therapy. N(CN)
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Marta Paradís-Bas, Judit Tulla-Puche, Fernando Albericio. Page ID 20965; Table of contents. -alkyl carbamates with aryl halides and arylboronic acids. Recent Progress in the Chemical Synthesis of Class II and S-Glycosylated Bacteriocins. Parker, Christian E. Schafmeister. Protection strategies for directionally-controlled synthesis of previously inaccessible metal–organic polyhedra (MOPs): the cases of carboxylate- and amino-functionalised Rh(
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or check out our status page at https://status.libretexts.org. Protein Chemical Synthesis by SEA Ligation. 2-Methoxyphenyl isocyanate: a chemoselective multitasking reagent for an amine protection/deprotection sequence. Chemical Synthesis of Antimicrobial Peptides. Christine A. Arbour, Thilini D. Kondasinghe, Hasina Y. Saraha, Teanna L. Vorlicek, Jennifer L. Stockdill.
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Consider the reactivity of different hydroxyl groups! Yahya E. Jad, Thavendran Govender, Hendrik G. Kruger, Ayman El-Faham, Beatriz G. de la Torre, and Fernando Albericio . You have to login with your ACS ID befor you can login with your Mendeley account. Chu Jing, Yasuhito Suzuki, Akikazu Matsumoto. 2,2′-Dithiobis(5-nitropyridine) (DTNP) as an effective and gentle deprotectant for common cysteine protecting groups. Toward solid-phase peptide fragment ligation by a traceless-Ugi multicomponent reaction approach. Synthesis of Deshydroxy Skyllamycins A–C. Synthesis and Analysis of the Conformational Preferences of 5-Aminomethyloxazolidine-2,4-dione Scaffolds: First Examples of β
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