116798-35-7Relevant academic research and scientific papers
Iminophosphorane-mediated synthesis of cyclic guanidines: Application to the synthesis of a simplified NA22598A1 analogue
Nalli, Stefano M.,Clarkson, Guy J.,Franklin, Alison S.,Bellone, Graziella,Shipman, Michael
experimental part, p. 2339 - 2341 (2009/05/07)
Reaction of Cbz-protected β-amino azides with bis(diphenylphosphino) butane and tosyl isocyanate provides differentially substituted 2-iminoimidazolidines in good yields. Georg Thieme Verlag Stuttgart.
Fluorous (trimethylsilyl)ethanol: A new reagent for carboxylic acid tagging and protection in peptide synthesis
Fustero, Santos,Sancho, Amador Garcia,Chiva, Gema,Sanz-Cervera, Juan F.,Del Pozo, Carlos,Acena, Jose Luis
, p. 3299 - 3302 (2007/10/03)
Starting with a fluorous analogue of 2-(trimethylsilyl)ethanol, we have designed an easy method for preparing a new fluorous tag (FTMSE) for the protection of carboxylic acids. Because mild conditions are employed in the tag cleavage (TBAF in the presence of 4 A molecular sieves, which prevent racemization), this tag can be advantageously used in the synthesis of peptides and modified peptides, as we have demonstrated with several examples, including the fluorous synthesis of short α- and β-peptides as well as of modified fluorinated retropeptides.
Synthesis of the amide analog of alternariolide (AM-toxin I), a host specific phytotoxin for apple leaves
Sakai, Mitsuru,Okuno, Toshikatsu,Hashimoto, Kimiko,Shirahama, Haruhisa
, p. 623 - 633 (2007/10/03)
The amide analog of alternariolide (AM-toxin I) was synthesized with high efficiency. The analog showed comparable biological activity to that of alternariolide.
