Protease-catalyzed peptide synthesis using inverse substrates: The influence of reaction conditions on the trypsin acyl transfer efficiency

1991 ◽  
Vol 38 (1) ◽  
pp. 104-108 ◽  
Author(s):  
Volker Schellenberger ◽  
Hans-Dieter Jakubke ◽  
Nina P. Zapevalova ◽  
Yuri V. Mitin
1986 ◽  
Vol 39 (11) ◽  
pp. 1747 ◽  
Author(s):  
AJ Liepa ◽  
AJ Liepa ◽  
TC Morton ◽  
TC Morton

Convenient preparations of synthetically useful acetals, a dithioacetal and an oxathiolan from the 2-acyl derivatives of 2-hydroxyaryl aldehydes under basic conditions are described. The mildness of the reaction conditions is illustrated by the formation of an ethoxycarbonyl -substituted dioxolan . The reaction is dependent upon an intramolecular acetyl group transfer and the mechanism of the reaction is discussed. Some broader implications of this type of acyl transfer are discussed.


Author(s):  
Siva S. Panda ◽  
Rachel A. Jones ◽  
C. Dennis Hall ◽  
Alan R. Katritzky

2003 ◽  
Vol 68 (24) ◽  
pp. 9247-9254 ◽  
Author(s):  
Derrick L. J. Clive ◽  
Soleiman Hisaindee ◽  
Don M. Coltart

2021 ◽  
Author(s):  
Chandrakanta Parida ◽  
Subhas C Pan

An organocatalytic asymmetric Michael/acyl transfer reaction between α-nitroketones and 4-arylidene-pyrrolidine-2,3-diones was reported. Bifunctional thiourea catalyst was found to be effective for this reaction. With 10 mol% of the catalyst, good results were attained for a variety of 1,5-dihydro-2H-pyrrol-2-ones under mild reaction conditions.


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