83451-16-5Relevant articles and documents
Peptide fragment coupling using a continuous-flow photochemical rearrangement of nitrones
Zhang, Yuan,Blackman, Melissa L.,Leduc, Andrew B.,Jamison, Timothy F.
, p. 4251 - 4255 (2013/05/08)
Go with the flow: A general approach for amide bond formation by way of a continuous-flow photochemical rearrangement of nitrones was described (see scheme). Simple aryl-alkyl amide bonds as well as complex peptide bonds were constructed efficiently with a residence time less than 20minutes. A tetrapeptide was synthesized in this way and the method could be applied to peptide fragment coupling. Copyright
Fungicides
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, (2008/06/13)
Use as agricultural fungicides of N-acyl-N-hydroxyalkanoic acid compounds of the formula STR1 and salts thereof, wherein each of the symbols has an assigned meaning.
Biogenetic type synthesis of penicillin cephalosporin antibiotics. I. A stereocontrolled synthesis of the penam and cephem ring systems from an acyclic tripeptide equivalent
Nakatsuka,Tanino,Kishi
, p. 5008 - 5010 (2007/10/08)
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