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.
A releasable disulfide carbonate linker for molecular hydrogelations
Liu, Qicai,Ou, Caiwen,Ren, Chunhua,Wang, Ling,Yang, Zhimou,Chen, Minsheng
, p. 1556 - 1559 (2012)
We used a releasable disulfide carbonate linker to construct precursors of gelators and form stable gels.
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.
Design and synthesis of a novel peptidomimetic inhibitor of HIV-1 Tat-TAR interactions: Squaryldiamide as a new potential bioisostere of unsubstituted guanidine
Lee, Chi-Wan,Cao, Hong,Ichiyama, Kozi,Rana, Tariq M.
, p. 4243 - 4246 (2005)
By performing RNA-targeted structure-activity relationship studies, we discovered a novel peptidomimetic containing squaryldiamide as a potential bioisostere replacement for guanidine that binds transactivation responsive RNA with high affinity.
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-
Preparation method of triphosphate compound and deoxynucleotide
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Paragraph 0107-0109, (2020/11/23)
The invention discloses a preparation method of a triphosphate compound and deoxynucleotide. In the preparation method of the triphosphate compound, tetrahydrofuran is used for replacing trimethyl phosphate/triethyl phosphate, tri-n-propylamine is used for replacing tri-n-butylamine, and acetonitrile is used for replacing N,N-dimethylformamide; so that the preparation method has the advantages that the yield is high, few byproducts are produced, a solvent is easy to remove, and the triphosphate compound is non-toxic, safe and the like. According to the preparation method of the deoxynucleotide, the morpholine dimethylformamide solution is used for replacing a triethylamine solution to remove the F-moc group, so that the reaction time is greatly shortened, the generation of byproducts is reduced, and the yield is improved.
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
MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS
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Paragraph 001283, (2018/09/12)
Provided herein are antibacterial compounds, wherein the compounds in some embodiments have broad spectrum bioactivity. In various embodiments, the compounds act by inhibition of bacterial type 1 signal peptidase (SpsB), an essential protein in bacteria. Pharmaceutical compositions and methods for treatment using the compounds described herein are also provided.
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
Base-Free Iridium-Catalyzed Hydrogenation of Esters and Lactones
Brewster, Timothy P.,Rezayee, Nomaan M.,Culakova, Zuzana,Sanford, Melanie S.,Goldberg, Karen I.
, p. 3113 - 3117 (2016/07/06)
Half-sandwich iridium bipyridine complexes catalyze the hydrogenation of esters and lactones under base-free conditions. The reactions proceed with a variety of ester and lactone substrates. Mechanistic studies implicate a pathway involving rate-limiting hydride transfer to the substrate at high pressures of H2 (≥50 bar).