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Items: 1 to 20 of 87

1.

Investigation of the ring-closing metathesis of peptides in water.

Cochrane SA, Huang Z, Vederas JC.

Org Biomol Chem. 2013 Jan 28;11(4):630-9. doi: 10.1039/c2ob26938d. Epub 2012 Dec 4.

PMID:
23212663
2.

Synthesis of biologically active dicarba analogues of the peptide hormone oxytocin using ring-closing metathesis.

Stymiest JL, Mitchell BF, Wong S, Vederas JC.

Org Lett. 2003 Jan 9;5(1):47-9.

PMID:
12509887
3.

Synthesis of oxytocin analogues with replacement of sulfur by carbon gives potent antagonists with increased stability.

Stymiest JL, Mitchell BF, Wong S, Vederas JC.

J Org Chem. 2005 Sep 30;70(20):7799-809.

PMID:
16277299
4.

A role for ring-closing metathesis in medicinal chemistry: mimicking secondary architectures in bioactive peptides.

Pérez de Vega MJ, García-Aranda MI, González-Muñiz R.

Med Res Rev. 2011 Sep;31(5):677-715. doi: 10.1002/med.20199. Epub 2010 Jan 14. Review.

PMID:
20077561
5.

Synthesis of stapled beta3-peptides through ring-closing metathesis.

Bergman YE, Del Borgo MP, Gopalan RD, Jalal S, Unabia SE, Ciampini M, Clayton DJ, Fletcher JM, Mulder RJ, Wilce JA, Aguilar MI, Perlmutter P.

Org Lett. 2009 Oct 1;11(19):4438-40. doi: 10.1021/ol901803d.

PMID:
19719157
6.

Synthesis of oxytocin antagonists containing conformationally constrained amino acids in position 2.

Tóth GK, Bakos K, Penke B, Pávó I, Varga C, Török G, Péter A, Fülöp F.

Bioorg Med Chem Lett. 1999 Mar 8;9(5):667-72.

PMID:
10201826
7.

Trimethoxyphenylthio as a highly labile replacement for tert-butylthio cysteine protection in Fmoc solid phase synthesis.

Postma TM, Giraud M, Albericio F.

Org Lett. 2012 Nov 2;14(21):5468-71. doi: 10.1021/ol3025499. Epub 2012 Oct 17.

PMID:
23075145
8.

Synthesis of all-hydrocarbon stapled α-helical peptides by ring-closing olefin metathesis.

Kim YW, Grossmann TN, Verdine GL.

Nat Protoc. 2011 Jun;6(6):761-71. doi: 10.1038/nprot.2011.324. Epub 2011 May 12.

PMID:
21637196
9.

Alpha,alpha-disubstituted glycines bearing a large hydrocarbon ring: peptide self-assembly through hydrophobic recognition.

Ohwada T, Kojima D, Kiwada T, Futaki S, Sugiura Y, Yamaguchi K, Nishi Y, Kobayashi Y.

Chemistry. 2004 Feb 6;10(3):617-26.

PMID:
14767925
10.

Step-wise and pre-organization induced synthesis of a crossed alkene-bridged nisin Z DE-ring mimic by ring-closing metathesis.

Ghalit N, Kemmink J, Hilbers HW, Versluis C, Rijkers DT, Liskamp RM.

Org Biomol Chem. 2007 Mar 21;5(6):924-34. Epub 2007 Feb 7.

PMID:
17340008
11.

Bidirectional solid-phase peptide synthesis. Extension of the dinitrophenylene-bridging method to cysteine-containing peptides.

Glass JD, Talansky A, Grzonka Z, Schwartz IL, Walter R.

J Am Chem Soc. 1974 Oct 2;96(20):6476-80. No abstract available.

PMID:
4412184
12.

Directed N-terminal elongation of unprotected peptides catalyzed by cathepsin C in water.

Gittel C, Schmidtchen FP.

Bioconjug Chem. 1995 Jan-Feb;6(1):70-6.

PMID:
7711107
13.

Disulfide bond-forming reaction using a dimethyl sulfoxide/aqueous HCl system and its application to regioselective two disulfide bond formation.

Tamamura H, Otaka A, Nakamura J, Okubo K, Koide T, Ikeda K, Ibuka T, Fujii N.

Int J Pept Protein Res. 1995 Apr;45(4):312-9.

PMID:
7601603
14.

Peptide-bound dinitrosyliron complexes (DNICs) and neutral/reduced-form Roussin's red esters (RREs/rRREs): understanding nitrosylation of [Fe-S] clusters leading to the formation of DNICs and RREs using a de novo design strategy.

Lin ZS, Lo FC, Li CH, Chen CH, Huang WN, Hsu IJ, Lee JF, Horng JC, Liaw WF.

Inorg Chem. 2011 Oct 17;50(20):10417-31. doi: 10.1021/ic201529e. Epub 2011 Sep 22.

PMID:
21939194
15.

Magnesium and biological activity of oxytocin analogues modified on aromatic ring of amino acid in position 2.

Slaninová J, Maletínská L, Vondrásek J, Procházka Z.

J Pept Sci. 2001 Aug;7(8):413-24.

PMID:
11548057
16.
17.

Solid-phase synthesis of oxytocin using iodotrichlorosilane as Boc deprotecting agent.

Sivanandaiah KM, Sureshbabu VV, Shankaramma SC.

Int J Pept Protein Res. 1995 Apr;45(4):377-9.

PMID:
7601611
18.

Introduction of all-hydrocarbon i,i+3 staples into alpha-helices via ring-closing olefin metathesis.

Kim YW, Kutchukian PS, Verdine GL.

Org Lett. 2010 Jul 2;12(13):3046-9. doi: 10.1021/ol1010449.

PMID:
20527740
19.
20.

Modification of constrained peptides by ring-closing metathesis reaction.

Kotha S, Sreenivasachary N, Mohanraja K, Durani S.

Bioorg Med Chem Lett. 2001 Jun 4;11(11):1421-3.

PMID:
11378368

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