LEADER 04057nam 2201153z- 450 001 9910674046603321 005 20210501 035 $a(CKB)5400000000042591 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/68334 035 $a(oapen)doab68334 035 $a(EXLCZ)995400000000042591 100 $a20202105d2021 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aMolecules from Side Reactions 210 $aBasel, Switzerland$cMDPI - Multidisciplinary Digital Publishing Institute$d2021 215 $a1 online resource (100 p.) 311 08$a3-0365-0004-9 311 08$a3-0365-0005-7 330 $aThe Special Issue "Molecules from Side Reactions" is a collection of papers reporting on the synthesis and characterization of the molecules that come from unexpected synthetic routes. This is the first example of a Special Issue based on such a topic, notwithstanding that all synthetic chemists have isolated a side product during a chemical reaction. Instead of continuing to store the side products in the freezer, I have thought to give them the dignity of publication, making them available to the scientific community. The short manuscripts collected here respect the principle of "one compound per paper" and have the purpose of preserving the molecular diversity deriving from a chemical reaction. The molecular scaffolds are unexpected and intriguing, and could be useful starting points or intermediates for exploring novel reactions. 606 $aHistory of engineering and technology$2bicssc 610 $a(E,Z)-isomerization 610 $a19F NMR spectroscopy 610 $a1H-pyrazolo[3,4-b]pyridine 610 $a3-acetyl-2,3-dihydro-1,3,4-oxadiazole 610 $a8-Fluoro-2'-deoxyguanosine 610 $aacadesine 610 $aAICAR 610 $aallenic compounds 610 $aAMPK 610 $aazaheterocycles 610 $abenzamides 610 $abidentate directing groups 610 $abis-chelates 610 $aC-glycosylation 610 $aC-H bond functionalization 610 $acaprazamycins 610 $acarbohydrate 610 $achelation assistance 610 $achlorinated nucleosides 610 $aconjugated diyne 610 $acopper 610 $acyanide 610 $acyclization 610 $adiacetal 610 $aepoxide 610 $aester group migration 610 $afluorinated nucleosides 610 $afluorination 610 $afuran 610 $aglycosyl sulfoxide 610 $aguanidinium 610 $aheterocycle 610 $ahydroxy methylation 610 $aketose 610 $aLAH reduction 610 $aligand 610 $amannose 610 $amodified nucleosides 610 $amuraymycins 610 $aN-alkylation 610 $aN-C bond cleavage 610 $aN'-acetylhydrazide 610 $an/a 610 $anetwork 610 $anitration 610 $anucleoside analogues 610 $anucleosides 610 $aorganic synthesis 610 $aoxazole 610 $aoxetane 610 $apent-1,2,3,4-tetraene intermediate 610 $aphosphoramidite 610 $aphosphorylation 610 $apsicose 610 $apyridine derivatives 610 $apyridine-imidazolium 610 $arare sugar 610 $arearrangement 610 $aribose 610 $aRORC reaction 610 $aseven-membered rings 610 $asolid phase synthesis 610 $aspiro-oxetane 610 $athioglycoside oxidation 610 $aunexpected iminium cation 610 $auridine 610 $auronate 610 $aX-ray structure determination 615 7$aHistory of engineering and technology 700 $aD'Errico$b Stefano$4edt$0605153 702 $aD'Errico$b Stefano$4oth 906 $aBOOK 912 $a9910674046603321 996 $aMolecules from Side Reactions$93059531 997 $aUNINA