149296-97-9Relevant academic research and scientific papers
Evaluation of the final deprotection system for the solid-phase synthesis of tyr(SO3H)-containing peptides with 9-fluorenylmethyloxycarbonyl (Fmoc)-strategy and its application to the synthesis of cholecystokinin (CCK)-12
Yagami,Shiwa,Futaki,Kitagawa
, p. 376 - 380 (1993)
Acidolytic deprotection and cleavage conditions for an acid-labile Tyr(SO3H)-containing peptide were systematically examined with respect to acid, temperature, and scavenger. The 90% aqueous trifluoroacetic acid (TFA)-based reagent systems (90%
COMPOUNDS FOR AMIDE-FORMING REACTIONS
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Page/Page column 28; 29, (2014/01/07)
Provided herein is a compound of Formula I, that displays remarkable physicochemical properties as a peptide-coupling additive for peptide-forming reactions in water, wherein said coupling reactions proceed without measurable racemization. A method of pro
A new oxyma derivative for nonracemizable amide-forming reactions in water
Wang, Qinghui,Wang, Yong,Kurosu, Michio
supporting information; experimental part, p. 3372 - 3375 (2012/09/07)
An Oxyma derivative, (2,2-dimethyl-1,3-dioxolan-4-yl)methyl 2-cyano-2-(hydroxyimino)acetate (2), displayed remarkable physicochemical properties as a peptide-coupling additive for peptide-forming reactions in water. Short peptides to oligopeptides could b
