About: p-Nitrobenzyloxycarbonyl (pNZ) as a TemporaryNα-Protecting Group in Orthogonal Solid-Phase Peptide Synthesis - Avoiding Diketopiperazine and Aspartimide Formation

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About: p-Nitrobenzyloxycarbonyl (pNZ) as a TemporaryNα-Protecting Group in Orthogonal Solid-Phase Peptide Synthesis - Avoiding Diketopiperazine and Aspartimide Formation Goto Sponge NotDistinct Permalink

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article published in 2005

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rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в липні 2005 (uk) im Juli 2005 veröffentlichter wissenschaftlicher Artikel (de) article published in 2005 (en)
publication date	wds:Q58035687-89B4D5B5-EC2A-467E-8758-E6F986AC0E6B
publication date	2005-07-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q58035687-00950645-F35A-47F6-BB7D-7E7C77BADBF6 wds:Q58035687-109FB332-2FA4-432F-AB81-51F137A0470C wds:Q58035687-168D1775-F9F5-46D0-9B58-655B08C9EB4B wds:Q58035687-1B505A99-077C-4992-AB8D-DC1123A1954D wds:Q58035687-37E3FAA0-9B0E-423E-B0B1-D49800AB5966 wds:Q58035687-3A62E90B-FA9F-4DB8-9420-3E4F0E8CD4DA wds:Q58035687-45B41B82-7BDD-45E8-9913-7369AE693AF7 wds:Q58035687-56D0ECA7-FF08-45D3-87E6-81F8399B9068 wds:Q58035687-5B2078C7-AA7A-4DD6-BE23-E1FFEA0665A6 wds:Q58035687-69202E82-B5A7-4F61-B8A8-72C2BCA8CE26 wds:Q58035687-6BA5D195-7907-495E-8D18-E4DE19B0F938 wds:Q58035687-723D03FB-90DC-4524-AC70-1CD3A69591E6 wds:Q58035687-779BEDB8-9EB3-4C3E-813C-6185B7D33E38 wds:Q58035687-7DD46F5C-156E-4E4A-B8F4-E4A8AA39F532 wds:Q58035687-80C9629E-DE8F-4B31-8760-EB1598DC88E9 wds:Q58035687-81153928-7553-4E74-92B7-0DCCE49A6EAD wds:Q58035687-877232F0-8919-44D4-8898-38069239D6A0 wds:Q58035687-8CD7BAE2-CC1D-4DD8-B933-8F47343A6929 wds:Q58035687-90DC20AB-A0B7-475C-B970-EE48FD5926B8 wds:Q58035687-A035D9AA-1266-4C6B-A948-9D61040672A8 wds:Q58035687-A1AC08F4-548F-410B-A6FE-6B3A40AB5192 wds:Q58035687-AD32E0FA-6279-4A24-81A9-2A088A493032 wds:Q58035687-B423D8F7-8714-49BA-8D88-691E096E9398 wds:Q58035687-B528F736-0A65-4A14-B9B7-9DA46A6E0361 wds:Q58035687-BAEFC177-45E2-4B91-AD7E-397AEA42E5B3 wds:Q58035687-BBB2E9CC-2652-41D3-9E7F-83643C1AE6D6 wds:Q58035687-BD536A7D-4162-420B-812A-E2FC2A0A3436 wds:Q58035687-CDA888BE-0730-4A83-85C9-E81EFB05778D wds:Q58035687-DA28B9C4-EE6F-4566-8090-8BE59DC10328 wds:Q58035687-DC1F9D40-776F-408A-B285-82516D95F79D wds:Q58035687-E49E1B3E-4AFE-49FE-9B5E-43D9FD50077B wds:Q58035687-ED391799-A60A-4D83-8464-22EB9FCF976D wds:Q58035687-F37ECC7E-0BA8-4535-B168-6A8D62059405 wds:Q58035687-F7732969-485B-4DBD-A72A-C338874003CB wds:Q58035687-FE8D8A6A-36E8-4901-9140-B013E73574C5
cites work	Use of Onium Salt-Based Coupling Reagents in Peptide Synthesis1 Use of Alloc-amino acids in solid-phase peptide synthesis. Tandem deprotection-coupling reactions using neutral conditions Solid phase synthesis Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide Orthogonal protecting groups for N(alpha)-amino and C-terminal carboxyl functions in solid-phase peptide synthesis An HPLC-ESMS study on the solid-phase assembly ofC-terminal proline peptides Diketopiperazine formation in solid phase peptide synthesis using p-alkoxybenzyl ester resins and Fmoc-amino acids Peptides as drugs: is there a market? Design, synthesis and early structure-activity relationship of farnesyltransferase inhibitors which mimic both the peptidic and the prenylic substrate Preparation of head-to-tail cyclic peptides via side-chain attachment: implications for library synthesis. Therapeutic peptides Monitoring the solid-phase synthesis of depsides and depsipeptides. A color test for hydroxyl groups linked to a resin The aspartimide problem in Fmoc-based SPPS. Part I. A new amino protecting group removable by reduction. Chemistry of the dithiasuccinoyl (Dts) function Synthesis, Resolution, and Applications of 1,16-Dihydroxytetraphenylene as a Novel Building Block in Molecular Recognition and Assembly1 Use of N-tritylamino acids and PyAOP1 for the suppression of diketopiperazine formation in Fmoc/tBu solid-phase peptide synthesis using alkoxybenzyl ester anchoring linkages Use of BOP reagent for the suppression of diketopiperazine formation in boc/bzl solid-phase peptide synthesis Application of N,N-dimethylformamide dineopentyl acetal for efficient anchoring of N alpha-9-fluorenylmethyloxycarbonylamino acids as p-alkoxybenzyl esters in solid-phase peptide synthesis Improved approach for anchoring N alpha-9-fluorenylmethyloxycarbonylamino acids as p-alkoxybenzyl esters in solid-phase peptide synthesis From Production of Peptides in Milligram Amounts for Research to Multi-Tons Quantities for Drugs of the Future 3-(1-Piperidinyl)alanine formation during the preparation ofC-terminal cysteine peptides with the Fmoc/t-Bu strategy Carboxyl-catalyzed intramolecular aminolysis. Side reaction in solid-phase peptide synthesis The aspartimide problem in Fmoc-based SPPS. Part II. Aspartimide formation in base-driven 9-fluorenylmethoxycarbonyl chemistry “One-Pot” Preparation ofN-Carbamate Protected Amino Acids via the Azide Specific removal of o-methoxybenzyl protection by DDQ oxidation Failure sequence in solid-phase peptide synthesis due to the presence of an N-alkylamino acid. Solid-Phase Strategies for the Assembly of Template-Based Protein Mimetics1 Four-dimensional orthogonal solid-phase synthesis of new scaffolds based on cyclic tetra-β-peptides Design of protecting groups for the beta-carboxylic group of aspartic acid that minimize base-catalyzed aspartimide formation Synthesis of polyfunctionalized biphenyls as intermediates for a new class of liquid crystals Synthesis of peptide sequences related to thrombospondin: factors affecting aspartimide by-product formation Amino-acids condensations in the preparation of N alpha-9-fluorenylmethyloxycarbonylamino-acids with 9-fluorenylmethylchloroformate N-p-nitrobenzyloxycarbonyl galactosamine imidate as a glycosyl donor for the efficient synthesis of mucin core-2 analogue
author name string	wds:Q58035687-01FE32C8-F4C3-4958-B5CA-A23E9D6B5D15 wds:Q58035687-A42A042D-7706-4ED1-83DC-5F1912B59FC6 wds:Q58035687-C4BEC462-9391-4891-AE4B-81460D52B410 wds:Q58035687-DCB153E0-60CF-45B6-9CE3-81EDBE509BFA
author name string	Fernando Albericio Albert Isidro-Llobet Mercedes Álvarez Judit Guasch-Camell
rdfs:label	p-Nitrobenzyloxycarbonyl (nl) p-Nitrobenzyloxycarbonyl (pNZ) as a TemporaryNα-Protecting Group in Orthogonal Solid-Phase Peptide Synthesis - Avoiding Diketopiperazine and Aspartimide Formation (en)
skos:prefLabel	p-Nitrobenzyloxycarbonyl (nl) p-Nitrobenzyloxycarbonyl (pNZ) as a TemporaryNα-Protecting Group in Orthogonal Solid-Phase Peptide Synthesis - Avoiding Diketopiperazine and Aspartimide Formation (en)
name	p-Nitrobenzyloxycarbonyl (nl) p-Nitrobenzyloxycarbonyl (pNZ) as a TemporaryNα-Protecting Group in Orthogonal Solid-Phase Peptide Synthesis - Avoiding Diketopiperazine and Aspartimide Formation (en)
title	wds:Q58035687-C03F9208-9161-43FE-8D30-EA006156D2A1
title	p-Nitrobenzyloxycarbonyl (pNZ) as a TemporaryNα-Protecting Group in Orthogonal Solid-Phase Peptide Synthesis - Avoiding Diketopiperazine and Aspartimide Formation (en)
page(s)	wds:Q58035687-BBEB7167-5CBF-487F-8A53-CE7AF656A1B2
page(s)	3031-3039
instance of	wds:Q58035687-945D5E10-2C09-48FF-BED9-446C10163130
instance of	scholarly article
published in	wds:Q58035687-27D9D819-9BF3-4114-BA06-5D6F68FA9F2B
published in	European Journal of Organic Chemistry
issue	wds:Q58035687-1DE69E8D-6686-43E0-A5FF-49806D5F1122

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