Approach to the Synthesis of Natural and Modified Oligonucleotides by the Phosphotriester Method Using O-Nucleophilic Intramolecular Catalysis

By Efimov Vladimir   Molchanova Natalia   Chakhmakhcheva Oksana  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 26, Iss. 8-9, 2007-08 ,pp. : 1087-1093

Taylor & Francis Ltd

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Silyl Protecting Groups for Oligonucleotide Synthesis Removed by A ZnBr 2 Treatment

By Ferreira Fernando   Morvan François  

Nucleosides, Nucleotides & Nucleic Acids, Vol. 24, Iss. 5-7, 2005-04 ,pp. : 1009-1013

Taylor & Francis Ltd

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Reactivity of easily removable protecting groups for glycine in peptide synthesis using papain as catalyst - Influence of the n- protecting groups and the reaction medium composition

By Fite M.   Alvaro G.   Clapes P.   Lopez-Santin J.   Benaiges M.D.   Caminal G.  

Enzyme and Microbial Technology, Vol. 23, Iss. 3, 1998-08 ,pp. : 199-203

Elsevier

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New Hydrogen Donor: A Facile Method for the Removal of Hydrogenolysable Protecting Groups in Peptide Synthesis.

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Protein and Peptide Letters, Vol. 9, Iss. 3, 2002-06 ,pp. : 225-230

Bentham Science Publishers

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Efficient synthesis of nucleic acids heavily modified with non‐canonical ribose 2′‐groups using a mutantT7 RNA polymerase (RNAP)

By Padilla Robert   Sousa Rui  

Nucleic Acids Research, Vol. 27, Iss. 6, 1999-03 ,pp. : 1561-1563

Oxford University Press

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