Interesting scientific research on 610-09-3

There is still a lot of research devoted to this compound(SMILES:O=C([C@H]1[C@@H](C(O)=O)CCCC1)O)Recommanded Product: 610-09-3, and with the development of science, more effects of this compound(610-09-3) can be discovered.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 610-09-3, is researched, SMILESS is O=C([C@H]1[C@@H](C(O)=O)CCCC1)O, Molecular C8H12O4Journal, Journal of the American Chemical Society called Photoreduction of carbon dioxide to its radical anion by nickel cluster [Ni3(μ3-I)2(dppm)3]: formation of two carbon-carbon bonds via addition of carbon dioxide radical anion to cyclohexene, Author is Morgenstern, David A.; Wittrig, Rebecca E.; Fanwick, Phillip E.; Kubiak, Clifford P., the main research direction is photochem reduction carbon dioxide nickel cluster; cyclohexene photochem dicarboxylation.Recommanded Product: 610-09-3.

The trinuclear cluster Ni3(μ3-I)2(dppm)3, (1) [dppm = bis(diphenylphosphino)methane] is formed by conproportionation of Ni(COD)2 and NiI2 in the presence of dppm. Cluster 1 and its singly oxidized radical cation (2) have been characterized spectroscopically and by x-ray diffraction. Cluster 2 exhibits a slight Jahn-Teller distortion of its triangular nickel framework. Irradiation of 1 in the presence of CO2 results in photochem. electron transfer to produce CO2•- and 2. The CO2•- can be trapped by H-atom abstraction from toluene to produce formate ion or with cyclohexene to form cis- and trans-1,2-cyclohexanedicarboxylic acid. The radical anion disproportionation products, carbonate and CO, are observed in the absence of a trapping reagent for CO2•-.

There is still a lot of research devoted to this compound(SMILES:O=C([C@H]1[C@@H](C(O)=O)CCCC1)O)Recommanded Product: 610-09-3, and with the development of science, more effects of this compound(610-09-3) can be discovered.

Reference:
Benzisoxazole – Wikipedia,
Benzisoxazole – an overview | ScienceDirect Topics