5 results

Phytomanagement - Tavaux (F-39)

Disciplines : forestry mycology cell biology ...
Collected date : from 2011 ongoing

The site is located in Western Europe along a major river and surrounded by several urban aggregates. Production at the chlor- alkali facility began in 1950 with wastewater discharged directly to a stream. In 1964 a dam was constructed downstream of the discharge. A 12-ha area with dikes 5-m high ...

Phytomanagement - Thann (F-68)

Disciplines : forestry mycology remote sensing ...
Collected date : from Mar 2014 ongoing
Creators : Michel Chalot

The experimental site of Thann is located in the valley of the Thur in Alsace (France) near the border with Germany and Switzerland, on a 15 ha-chemistry-based industrial complex. The Thann plant owned by the TRONOX company is one of the most important sites for TiO2 production in Europe and is the ...

Antimicrobial Activity and DFT Studies of a Novel Set of Spiropyrrolidines Tethered with Thiochroman-4-one/Chroman-4-one Scaffolds

A novel series of 14 spiropyrrolidines bearing thiochroman-4-one/chroman-4-one, and oxindole/acenaphthylene-1,2-dione moieties were synthesized and characterized by spectroscopic techniques, as well as by three X-ray diffraction studies, corroborating the stereochemistry. Quantum chemical ...

Synthesis, antidiabetic activity and molecular docking study of rhodanine-substitued spirooxindole pyrrolidine derivatives as novel α-amylase inhibitors

In a sustained search for novel α-amylase inhibitors for the treatment of type 2 diabetes mellitus (T2DM), we report herein the synthesis of a series of nineteen novel rhodanine-fused spiro[pyrrolidine-2,3′-oxindoles]. They were obtained by one-pot three component [3 + 2] cycloaddition of stabilized ...

Diversity-oriented Synthesis of Spiropyrrolo[1, 2-a]isoquinoline Derivatives via Diastereoselective and Regiodivergent Three-component 1,3-Dipolar Cycloaddition Reactions: In vitro and in vivo Evaluation of the Antidiabetic Activity of Rhodanine Analogues

Collected date : from 2018 to 2021

An efficient diastereoselective route is developed to get access to novel spiropyrrolo[1,2-a]isoquinoline-oxindole skeletons by a one-potthree-component [3 + 2] cycloaddition reaction of (Z)-5-arylidene-1,3-thiazolidine-2,4-diones, isatin derivatives, and 1,2,3,4-tetrahydroisoquinoline (THIQ). ...

5 results

dat@UBFC

dat@UBFC is a metadata catalogue for research data produced at UBFC.

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Université de Bourgogne, Université de Franche-Comté, UTBM, AgroSup Dijon, ENSMM, BSB, Arts des Metiers