(Q58104607)

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Use of ozonolysis in the synthesis of C-terminal peptide aldehydes on solid support

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Use of ozonolysis in the synthesis of C-terminal peptide aldehydes on solid support (English)

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Jean Martinez

7

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Catherine Pothion

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1

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Marielle Paris

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2

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Annie Heitz

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3

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Luc Rocheblave

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4

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Florence Rouch

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5

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Jean-Alain Fehrentz

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6

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publication date

November 1997

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published in

Tetrahedron Letters

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volume

38

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issue

44

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page(s)

7749-7752

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cites work

Improved solid phase synthesis of C-terminal peptide aldehydes

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Inhibition studies of some serine and thiol proteinases by new leupeptin analogues

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Highly active and selective anticoagulants: D-Phe-Pro-Arg-H, a free tripeptide aldehyde prone to spontaneous inactivation, and its stable N-methyl derivative, D-MePhe-Pro-Arg-H

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A simple method for semi-synthesis of peptidyl-argininals as potent inhibitors of trypsin-like proteases

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Synthesis of aldehydic peptides inhibiting renin

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N-methoxy-n-methylamides as effective acylating agents

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An Efficient Synthesis of Optically Active α-(t-Butoxycarbonylamino)-aldehydes from α-Amino Acids

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10.1016/S0040-4039(97)10086-7

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(Q58104607)

Use of ozonolysis in the synthesis of C-terminal peptide aldehydes on solid support

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