PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Azides”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 973 records · Page 54Linked to original sources

Reduction of azides to primary amines in substrates bearing labile ester functionality. Synthesis of a PEG-solubilized, "Y"-shaped iminodiacetic acid reagent for preparation of folate-tethered drugs.

[formula: see text] Anhydride 3 is a useful reagent for the synthesis of triply linked drug conjugates. Examples using paclitaxel are provided. Conversion of the azido moiety to a primary amine in the presence of substrates bearing labile ester functionality requires the use of tin/mercaptan reducing system which includes methanol exchange equilibration to effect nitrogen-tin bond scission.

Amines↗

First synthesis of 1,2,3-triazolo-linked (1,6)-alpha-D-oligomannoses (triazolomannoses) by iterative Cu(I)-catalyzed alkyne-azide cycloaddition.

The iterative copper(I)-catalyzed cycloaddition (rt or microwave) between an ethynyl alpha-C-mannoside and alkyl 6-azido-alpha-C-mannoside derivatives was suited to the (1,6)-ligation between alpha-D-mannose units through 1,4-disubstituted triazole bridges, thus resulting in the formation of linear oligomers (80-90% yield) with alternating triazole and mannose fragments up to a triazolo-pentamannose derivative.

Alkynes↗

Ferromagnetic vs. antiferromagnetic coupling in bis(mu2-1,1-azido)dinickel(II) complexes with syn- and anti-conformations of the end-on azide bridges.

Reaction of a 1 : 1 : 1 molar ratio of NiCl(2), NaN(3) and H(2)L, a tetradentate ligand N-(2-pyridyl)methyl)-N,N-bis(2'-hydroxy-3',5'-dimethylbenzyl)amine in methanol in presence of Et(3)N results in a turquoise precipitate, which affords deep green crystals of [Ni(2)(HL)(2)(N(3))(2)]*1.5CH(2)Cl(2) (1) and [Ni(2)(HL)(2)(N(3))(2)]*H(2)O (2) upon crystallization from CH(2)Cl(2)-MeOH or THF-MeOH, respectively. Both complexes reveal distorted octahedral NiN(4)O(2) coordination environments around the Ni(ii) centers with bis(micro-1,1-azido) bridging ligands. Complex 1 displays an unprecedented small Ni-N-Ni bridge angle of 90.4 degrees , whereas 2 contains the said angle of av. 98.7 degrees lying in the usual range observed for other comparable structures. The variable-temperature magnetic susceptibility together with the variable-field, variable-temperature (VTVH) magnetization measurements discern different ground states of S(t) = 0 for 1 and S(t) = 2 for 2. The magnetic behaviours of these compounds are discussed in the context of the known bis(end-on azido) bridging dinickel(II) complexes.

Azides↗