Preparation of dl-2,3,4-trihydroxybutylarsonic acid and dl-2,3-dihydroxybutane-1,4-bis(arsonic acid): starting compounds for novel arsonolipids

Tsivgoulis, Gerasimos M.; Lala, Maria A.; Ioannou, Panayiotis V.

doi:10.1016/j.chemphyslip.2007.04.011

Cited by 8 publications

(1 citation statement)

References 39 publications

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“…Other mono‐arsonolipids have been synthesized in this way from 2,3,4‐trihydroxybutylarsonic acid, the product of ring‐opening of 3,4‐epoxybutane‐1,2‐diol by sodium arsenite . Pseudo‐arsonolipids analogues, containing bis ‐arsonic acid groups, have also be synthesized from epihalohydrin and 1,4‐dibromo‐2,3‐butanediol, respectively.…”

Section: Arsenolipids and Arsenoliposomesmentioning

confidence: 99%

Organic Arsenicals as Functional Motifs in Polymer and Biomaterials Science

Tanaka

Davis

Wilson

2018

Macromol. Rapid Commun.

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Arsenic (As) exhibits diverse (bio)chemical reactivity and biological activity depending upon its oxidation state. However, this distinctive reactivity has been largely overlooked across many fields owing to concerns regarding the toxicity of arsenic. Recently, a clinical renaissance in the use of arsenicals, including organic arsenicals that are known to be less toxic than inorganic arsenicals, alludes to the possibility of broader acceptance and application in the field of polymer and biomaterials science. Here, current examples of polymeric/macromolecular arsenicals are reported to stimulate interest and highlight their potential as a novel platform for functional, responsive, and bioactive materials.

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Section: Arsenolipids and Arsenoliposomesmentioning

confidence: 99%