497312

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Synthesis and characterization of a triazine dendrimer that sequesters iron(III) using 12 desferrioxamine B groups.

Jongdoo Lim et al.

Bioorganic & medicinal chemistry, 18(15), 5749-5753 (2010-07-10)

The synthesis of a third generation triazine dendrimer, 1, containing multiple, iron-sequestering desferrioxamine B (DFO) groups is described. Benzoylation of the hydroxamic acid groups of DFO and formation of a reactive dichlorotriazine provide the intermediate for reaction with the second

Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as factor Xa inhibitor.

Nishida H, et al.

Chemical & Pharmaceutical Bulletin, 49(10), 1237-1244 (2001)

Enzymatic synthesis, thermal and crystalline properties of a poly (β-amino ester) and poly (lactone-co-β-amino ester) copolymers.

Martino L, et al.

Polymer, 53(9), 1839-1848 (2012)

Synthesis, spectroscopy, and biological activity of heterobimetallic complexes containing Sn (IV) and Pd (II) with 4-(hydroxymethyl) piperidine-1-carbodithioic acid.

Anwar MT, et al.

Russ. J. Gen. Chem., 83(12), 2380-2385 (2013)

Expedient protocol for solid-phase synthesis of secondary and tertiary amines.

Christian A Olsen et al.

Organic letters, 6(12), 1935-1938 (2004-06-05)

[reaction: see text] An expedient solid-phase synthetic approach to secondary and tertiary amines was developed. The protocol employs conversion of resin-bound amino alcohols to the corresponding iodides, followed by iodide displacement with primary or secondary amines or with unprotected amino

Synthesis and structure-activity relationships of 2-phenyl-1-[(pyridinyl- and piperidinylmethyl)amino]-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents.

Francis Giraud et al.

Bioorganic & medicinal chemistry letters, 19(2), 301-304 (2008-12-19)

Continuous efforts on the synthesis and structure-activity relationships (SARs) studies of modified 1-benzylamino-2-phenyl-3-(1H-1,2,4-triazol-1-yl)propan-2-ols as antifungal agents, allowed identification of new 1-[(pyridinyl- and piperidinylmethyl)amino] derivatives with MIC(80) values ranging from 1410.0 to 23.0ngmL(-1) on Candidaalbicans. These results confirmed both the importance

Standard molar enthalpies of formation of 2-, 3-, and 4-piperidinomethanol isomers.

da Silva MAVR and Cabral JITA

The Journal of Chemical Thermodynamics, 38(8), 1008-1012 (2006)

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