105496-31-9Relevant articles and documents
A multifunctional anomeric linker for the chemoenzymatic synthesis of complex oligosaccharides
Prudden, Anthony R.,Chinoy, Zoeisha S.,Wolfert, Margreet A.,Boons, Geert-Jan
, p. 7132 - 7135 (2014)
A new anomeric linker has been developed that facilitates the purification of glycans prepared by chemoenzymatic approaches and can readily give compounds that are appropriately modified for microarray development or glycan derivatives with a free reducing end that are needed as standards for the development of analytical protocols.
Repetitive solid-phase synthesis of polyamines
J?nsson, Daniel,Undén, Anders
, p. 3125 - 3128 (2002)
A repetitive solid-phase method for the synthesis of polyamines is described. Primary amino groups attached to a crosslinked polystyrene resin are monoalkylated by acid labile, benzhydryl-based alkyl chlorides. Reductive alkylation of the resulting secondary amino group by Fmoc-protected aminoaldehydes gives a N-benzhydryl polyamine backbone. Treatment of the resin with trifluoroacetic acid cleaves both the benzhydryl protective group and the polyamine derivative from the resin. By using benzhydryl protective groups with different acid stability, unbranched, branched and partly branched polyamines are synthesized.
Alcohols immobilization onto 2-chlorotritylchloride resin under microwave irradiation
Rizzi, Luca,Cendic, Katarina,Vaiana, Nadia,Romeo, Sergio
, p. 2808 - 2811 (2011)
The immobilization of alcohols onto 2-chlorotritylchloride resin using microwave irradiation was studied. Three different Fmoc-aminoalcohols were tested: the phenol-like Fmoc-tyramine, the primary alcohol Fmoc-ethanolamine, and the secondary alcohol Fmoc-
Method for stereoselective preparation of beta type single/double artemisinin (symmetric and asymmetric) alkyl ether amine maleate
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Paragraph 0057; 0066-0069, (2019/01/08)
The invention relates to the field of organic synthesis and pharmaceutical intermediates, particularly to a method for stereoselective preparation of beta type single/double artemisinin (symmetric andasymmetric) alkyl ether amine maleate. The method compr
Fast and Facile Synthesis of 4-Nitrophenyl 2-Azidoethylcarbamate Derivatives from N-Fmoc-Protected α-Amino Acids as Activated Building Blocks for Urea Moiety-Containing Compound Library
Chen, Ying-Ying,Chang, Li-Te,Chen, Hung-Wei,Yang, Chia-Ying,Hsin, Ling-Wei
, p. 131 - 136 (2017/04/24)
A fast and facile synthesis of a series of 4-nitrophenyl 2-azidoethylcarbamate derivatives as activated urea building blocks was developed. The N-Fmoc-protected 2-aminoethyl mesylates derived from various commercially available N-Fmoc-protected α-amino ac
