Synthesis of α-oxycarbanilinophosphonates and their anticholinesterase activities: the most potent derivative is bound to the peripheral site of acetylcholinesterase

Kaboudin, Babak; Emadi, Saeed; Faghihi, Mohammad Reza; Fallahi, Maryam; Sheikh-Hasani, Vahid

doi:10.3109/14756366.2012.663362

Cited by 9 publications

(1 citation statement)

References 36 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…[142] Later on, Kaboudin and Fallahi [143] modified the latter method via using magnesium oxide in absence of solvent and under ultrasonic irradiation or using the microwave irradiation. [144] In another publication, Yavari et al [145] reported the preparation of β-lactamphosphonates 124 in ≈ 96 % through one-pot reaction of P(OR) 3 , dibenzoylacetylene and phenylsulfonyl isocyanate at r.t. and in few minutes reaction time (Scheme 53).…”

Section: Reactions With Isocyanates and Isothiocyanatesmentioning

confidence: 98%

Investigations of the Chemistry of Alkyl Phosphites Toward Nitrogen-Containing Compounds: Efficient Approaches to α-Amino-, β-Amino-, and/or Enaminophosphonates

Abdou

Barghash

Bekheit

2015

Synthetic Communications

View full text Add to dashboard Cite

In this study, we report recent investigations of the chemical reactivity of alkyl phosphites mainly trialkyl and dialkyl phosphites with molecules containing different nitrogen-containing compounds reported by us and other research groups over the last twenty five years. Earlier leader important reports were also considered. The reviewed investigations in this article are customized, only according to the type of the nitrogenfunctional groups: [amines (primary, secondary, and tertiary amines), imines, amides, thioamides, nitriles, isocyanates, isothiocyanates, oximes, hydrazones, diazo, and azides]and not according to the site of attack or the final products. Furthermore, the present review article focuses on the synthesis of α-amino-, β-amino-and/or enaminophosphonates. These compounds occupy an important role in pharmaceutical chemistry.2 GRAPHICAL ABSTRACT:

show abstract

Section: Reactions With Isocyanates and Isothiocyanatesmentioning

confidence: 98%