The Nim-(2,4-dimethylpent-3-yloxycarbonyl)(Doc) group, a new nucleophile-resistant, HF-cleavable protecting group for histidine in peptide synthesis

Amelie Karlström and Anders Undén

Chem. Commun., 1996, 959
DOI: 10.1039/CC9960000959

One Pot N‐Protection of Amino Acids

Chr. Becu, M.‐F. Reyniers, M. J. O. Anteunis and R. Callens

Bulletin des Soc Chimique, 1990, 99, 779
DOI: 10.1002/bscb.19900991003

Explorations on the Total Synthesis of the Unusual Marine Alkaloid Chartelline A

Cuixiang Sun, Xichen Lin and Steven M. Weinreb

J. Org. Chem., 2006, 71, 3159
DOI: 10.1021/jo060084f

ARGININE, HISTIDINE AND TRYPTOPHAN IN PEPTIDE SYNTHESIS. THE IMIDAZOLE FUNCTION OF HISTIDINE

Barbara Rzeszotarska and Elzbieta Masiukiewicz

Organic Preparations and Procedures International, 1989, 21, 393
DOI: 10.1080/00304948909356412

A comparison of Boc and Fmoc SPPS strategies for the preparation of C‐terminal peptide α‐thiolesters: NY‐ESO‐1 39Cys‐68Ala‐COSR

Paul W. R. Harris and Margaret A. Brimble

Biopolymers, 2013, 100, 356
DOI: 10.1002/bip.22223

Structure-activity relationships of interleukin-8 determined using chemically synthesized analogs. Critical role of NH2-terminal residues and evidence for uncoupling of neutrophil chemotaxis, exocytosis, and receptor binding activities.

I. Clark-Lewis, C. Schumacher, M. Baggiolini and B. Moser

Journal of Biological Chemistry, 1991, 266, 23128
DOI: 10.1016/S0021-9258(18)54472-0

Amino acid deletion products resulting from incomplete deprotection of the Boc group fromNπ-benzyloxymethylhistidine residues during solid-phase peptide synthesis

Kumiko Yoshizawa-Kumagaye, Yuji Nishiuchi, Hideki Nishio and Terutoshi Kimura

J. Peptide Sci., 2005, 11, 512
DOI: 10.1002/psc.657

H‐Gly‐Hisψ(NHCO)Lys‐OH, partially modified retro‐inverso analogue of the growth factor glycyl‐L‐histidyl‐L‐lysine with enhanced enzymatic stability

ALMA DALPOZZO, KAROLY KANAI, GÉZA KERESZTURI and GERARDO CALABRESE

International Journal of Peptide and Protein Research, 1993, 41, 561
DOI: 10.1111/j.1399-3011.1993.tb00478.x

Extent of Nucleophilic Participation in the Solvolyses of an Aryl Chloromethyl Ether, α, p-Dichloroanisole

Byoung-Chun Park and Dennis N. Kevill

Journal of Chemical Research, 2013, 37, 483
DOI: 10.3184/174751913X13734534378121

Preparation of peptidic α-hydroxy phosphonates a new class of transition state analog renin inhibitors

Dinesh V. Patel, Katherine Rielly-Gauvin and Denis E. Ryono

Tetrahedron Letters, 1990, 31, 5587
DOI: 10.1016/S0040-4039(00)97903-6

Synthesis of (+)-pilocarpine analogs with a 2-oxazolidone structure

F. Bermejo Gonzalez, J. Perez Baz and M.I. Ruano Espina

Tetrahedron Letters, 1989, 30, 2145
DOI: 10.1016/S0040-4039(01)93734-7

Internal chain cleavage and product heterogeneity during Edman degradation of isosteric peptide analogs lacking the α‐carbonyl function

John Hempel, Klas Nilsson, Krister Larsson and Hans Jörnvall

FEBS Letters, 1986, 194, 333
DOI: 10.1016/0014-5793(86)80112-0

Problems associated with use of the benzyloxymethyl protecting group for histidines Formaldehyde adducts formed during cleavage by hydrogen fluoride 1

MARK A. MITCHELL, THOMAS A. RUNGE, W. RODNEY MATHEWS, AVNEET K. ICHHPURANI, NANCY K. HARN, PAUL J. DOBROWOLSKI and FRANCES M. ECKENRODE

International Journal of Peptide and Protein Research, 1990, 36, 350
DOI: 10.1111/j.1399-3011.1990.tb01293.x

Convergent solid-phase peptide synthesis. XI. Synthesis and purification of protected peptide segments spanning the entire sequence of the uteroglobin monomer using the photolabile nbb-resin.

Paul Lloyd-Williams, Margarida Gairí, Fernando Albericio and Ernest Giralt

Tetrahedron, 1993, 49, 10069
DOI: 10.1016/S0040-4020(01)80202-7

Synthesis and β‐conformation of sequential polypeptides containing arginine, histidine, and leucine

Bernard Barbier, Anita Caille and André Brack

Biopolymers, 1984, 23, 2299
DOI: 10.1002/bip.360231112

Facile formation of amide bonds between fragments containing unmasked imidazole‐ring systems. Synthesis of N‐[N‐[[[(5‐methyl‐4‐imidazolyl)methyl]thio]acetyl]‐L‐methionyl]histamine

Johan F. Modder, Barbara de Klerk‐Engels, Hubertus A. Ankersmit, Kees Vrieze and Gerard van Koten

Recl. Trav. Chim. Pays‐Bas, 1991, 110, 279
DOI: 10.1002/recl.19911100605

Potent Cyclic Monomeric and Dimeric Peptide Inhibitors of VLA-4 (?4?1 Integrin)-Mediated Cell Adhesion Based on the Ile-Leu-Asp-Val Tetrapeptide

Anand S. Dutta, Mandy Crowther, James J. Gormley, Lorraine Hassall, Christopher F. Hayward, Paul R. Gellert, Rod S. Kittlety, Peter J. Alcock, Alec Jamieson, Julie M. Moores, Amanda Rees, Linda J. Wood, Christopher F. Reilly and Duncan Haworth

J. Peptide Sci., 2000, 6, 321
DOI: 10.1002/1099-1387(200007)6:7<321::AID-PSC259>3.0.CO;2-A

Advances in Fmoc solid‐phase peptide synthesis

Raymond Behrendt, Peter White and John Offer

Journal of Peptide Science, 2016, 22, 4
DOI: 10.1002/psc.2836

Preparation of N(π)-alkyl- histamine and histidine derivatives through efficient alkylation followed by deprotection using activated silica gel

B.Moon Kim, Joon Shik Park and Jong Hyun Cho

Tetrahedron Letters, 2000, 41, 10031
DOI: 10.1016/S0040-4039(00)01792-5

Characterization of impurities in a synthetic renin substrate peptide by fast‐atom bombardment mass spectrometry and hybrid tandem mass spectrometry

W. Rodney Mathews, Thomas A. Runge, Peter E. Haroldsen, Simon J. Gaskell and K. B. Tomer

Rapid Comm Mass Spectrometry, 1989, 3, 314
DOI: 10.1002/rcm.1290030912

In search of new methods in peptide synthesis. A review of the last three decades

MIKLOS BODANSZKY

International Journal of Peptide and Protein Research, 1985, 25, 449
DOI: 10.1111/j.1399-3011.1985.tb02200.x

Aspartimide formation in peptide chemistry: occurrence, prevention strategies and the role of N-hydroxylamines

Ramon Subirós-Funosas, Ayman El-Faham and Fernando Albericio

Tetrahedron, 2011, 67, 8595
DOI: 10.1016/j.tet.2011.08.046

Potent new inhibitors of human renin

M. Szelke, B. Leckie, A. Hallett, D. M. Jones, J. Sueiras, B. Atrash and A. F. Lever

Nature, 1982, 299, 555
DOI: 10.1038/299555a0

Histidine racemization in the synthesis of an analog of the lutenizing hormone releasing factor

RÜDIGER PIPKORN and BJÖRN EKBERG

International Journal of Peptide and Protein Research, 1986, 27, 583
DOI: 10.1111/j.1399-3011.1986.tb01053.x