Matches in SemOpenAlex for { <https://semopenalex.org/work/W2943971104> ?p ?o ?g. }
- W2943971104 abstract "This review focuses on the use of dialkyl carbonates (DACs) as green reagents and solvents for the synthesis of several 5- and 6-membered heterocycles including: tetrahydrofuran and furan systems, pyrrolidines, indolines, isoindolines, 1,4-dioxanes, piperidines, and cyclic carbamates. Depending on the heterocycle investigated, the synthetic approach used was different. Tetrahydrofuran systems, pyrrolidines, indolines, isoindoline, and 1,4-dioxanes were synthesized using dimethyl carbonate (DMC) as sacrificial molecule (BAc2/BAl2 mechanism). Cyclic carbamates, namely 1,3-oxazin-2-ones, were prepared employing DACs as carbonylating agents, either by BAc2/BAl2 mechanism or through a double BAc2 mechanism. Piperidines were synthetized taking advantage of the anchimeric effect of a new family of dialkyl carbonates, i.e., mustard carbonates. Finally, in the case 5-hydroxymethylfurfural (HMF), DMC has been employed as efficient extracting solvent of this extensively investigated bio-based platform chemical from the reaction mixture. These synthetic approaches demonstrate, once again, the great versatility of DACs and their-yet to be fully explored-potential as green reagents and solvents in the synthesis of heterocycles." @default.
- W2943971104 created "2019-05-16" @default.
- W2943971104 creator A5030953268 @default.
- W2943971104 creator A5037198870 @default.
- W2943971104 creator A5089455790 @default.
- W2943971104 date "2019-05-07" @default.
- W2943971104 modified "2023-10-12" @default.
- W2943971104 title "Dialkyl Carbonates in the Green Synthesis of Heterocycles" @default.
- W2943971104 cites W1818242711 @default.
- W2943971104 cites W1966175157 @default.
- W2943971104 cites W1970310624 @default.
- W2943971104 cites W1970961575 @default.
- W2943971104 cites W1976550960 @default.
- W2943971104 cites W1978768457 @default.
- W2943971104 cites W1980284037 @default.
- W2943971104 cites W1980328276 @default.
- W2943971104 cites W1983047028 @default.
- W2943971104 cites W1986238541 @default.
- W2943971104 cites W1987100773 @default.
- W2943971104 cites W1987643155 @default.
- W2943971104 cites W1992066642 @default.
- W2943971104 cites W1999915031 @default.
- W2943971104 cites W2001488841 @default.
- W2943971104 cites W2003210552 @default.
- W2943971104 cites W2005877813 @default.
- W2943971104 cites W2006515463 @default.
- W2943971104 cites W2006951665 @default.
- W2943971104 cites W2009081386 @default.
- W2943971104 cites W2015353981 @default.
- W2943971104 cites W2016604961 @default.
- W2943971104 cites W2029613097 @default.
- W2943971104 cites W2034786874 @default.
- W2943971104 cites W2034824129 @default.
- W2943971104 cites W2036832988 @default.
- W2943971104 cites W2044902056 @default.
- W2943971104 cites W2046667467 @default.
- W2943971104 cites W2048194037 @default.
- W2943971104 cites W2049599251 @default.
- W2943971104 cites W2050305131 @default.
- W2943971104 cites W2051530293 @default.
- W2943971104 cites W2054207726 @default.
- W2943971104 cites W2055283267 @default.
- W2943971104 cites W2055615531 @default.
- W2943971104 cites W2058996815 @default.
- W2943971104 cites W2064699475 @default.
- W2943971104 cites W2077844490 @default.
- W2943971104 cites W2079466278 @default.
- W2943971104 cites W2085615226 @default.
- W2943971104 cites W2091218143 @default.
- W2943971104 cites W2094283941 @default.
- W2943971104 cites W2104465051 @default.
- W2943971104 cites W2111586715 @default.
- W2943971104 cites W2111920806 @default.
- W2943971104 cites W2117411428 @default.
- W2943971104 cites W2121449888 @default.
- W2943971104 cites W2131077784 @default.
- W2943971104 cites W2136032044 @default.
- W2943971104 cites W2136814861 @default.
- W2943971104 cites W2147933146 @default.
- W2943971104 cites W2149541027 @default.
- W2943971104 cites W2154282258 @default.
- W2943971104 cites W2164707672 @default.
- W2943971104 cites W2170214458 @default.
- W2943971104 cites W2289499926 @default.
- W2943971104 cites W2316809635 @default.
- W2943971104 cites W2321382274 @default.
- W2943971104 cites W2322788072 @default.
- W2943971104 cites W2324034725 @default.
- W2943971104 cites W2324845844 @default.
- W2943971104 cites W2334171950 @default.
- W2943971104 cites W2334282996 @default.
- W2943971104 cites W2336630029 @default.
- W2943971104 cites W2346430563 @default.
- W2943971104 cites W2541508156 @default.
- W2943971104 cites W2560101397 @default.
- W2943971104 cites W2747312923 @default.
- W2943971104 cites W2759158429 @default.
- W2943971104 cites W2766569351 @default.
- W2943971104 cites W2768765912 @default.
- W2943971104 cites W2769456954 @default.
- W2943971104 cites W2792397234 @default.
- W2943971104 cites W2901100949 @default.
- W2943971104 cites W2950709592 @default.
- W2943971104 cites W2950889221 @default.
- W2943971104 cites W2951550303 @default.
- W2943971104 cites W2951859706 @default.
- W2943971104 cites W2952330325 @default.
- W2943971104 cites W2952728229 @default.
- W2943971104 cites W2952852559 @default.
- W2943971104 cites W4211101698 @default.
- W2943971104 doi "https://doi.org/10.3389/fchem.2019.00300" @default.
- W2943971104 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6514103" @default.
- W2943971104 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31134180" @default.
- W2943971104 hasPublicationYear "2019" @default.
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