TY - BOOK ID - 145174179 TI - Molecules from Side Reactions PY - 2021 PB - Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute DB - UniCat KW - History of engineering & technology KW - oxazole KW - furan KW - RORC reaction KW - (E,Z)-isomerization KW - nitration KW - azaheterocycles KW - N-C bond cleavage KW - pyridine-imidazolium KW - ribose KW - psicose KW - ketose KW - rare sugar KW - hydroxy methylation KW - AICAR KW - acadesine KW - phosphorylation KW - fluorination KW - fluorinated nucleosides KW - nucleoside analogues KW - modified nucleosides KW - chlorinated nucleosides KW - AMPK KW - organic synthesis KW - bidentate directing groups KW - benzamides KW - chelation assistance KW - bis-chelates KW - C-H bond functionalization KW - X-ray structure determination KW - N'-acetylhydrazide KW - 3-acetyl-2,3-dihydro-1,3,4-oxadiazole KW - 1H-pyrazolo[3,4-b]pyridine KW - heterocycle KW - oxetane KW - epoxide KW - rearrangement KW - carbohydrate KW - C-glycosylation KW - spiro-oxetane KW - ester group migration KW - glycosyl sulfoxide KW - uronate KW - thioglycoside oxidation KW - mannose KW - 8-Fluoro-2'-deoxyguanosine KW - 19F NMR spectroscopy KW - solid phase synthesis KW - phosphoramidite KW - muraymycins KW - caprazamycins KW - nucleosides KW - uridine KW - cyclization KW - seven-membered rings KW - conjugated diyne KW - LAH reduction KW - diacetal KW - pent-1,2,3,4-tetraene intermediate KW - ligand KW - pyridine derivatives KW - allenic compounds KW - N-alkylation KW - copper KW - cyanide KW - network KW - guanidinium KW - unexpected iminium cation KW - oxazole KW - furan KW - RORC reaction KW - (E,Z)-isomerization KW - nitration KW - azaheterocycles KW - N-C bond cleavage KW - pyridine-imidazolium KW - ribose KW - psicose KW - ketose KW - rare sugar KW - hydroxy methylation KW - AICAR KW - acadesine KW - phosphorylation KW - fluorination KW - fluorinated nucleosides KW - nucleoside analogues KW - modified nucleosides KW - chlorinated nucleosides KW - AMPK KW - organic synthesis KW - bidentate directing groups KW - benzamides KW - chelation assistance KW - bis-chelates KW - C-H bond functionalization KW - X-ray structure determination KW - N'-acetylhydrazide KW - 3-acetyl-2,3-dihydro-1,3,4-oxadiazole KW - 1H-pyrazolo[3,4-b]pyridine KW - heterocycle KW - oxetane KW - epoxide KW - rearrangement KW - carbohydrate KW - C-glycosylation KW - spiro-oxetane KW - ester group migration KW - glycosyl sulfoxide KW - uronate KW - thioglycoside oxidation KW - mannose KW - 8-Fluoro-2'-deoxyguanosine KW - 19F NMR spectroscopy KW - solid phase synthesis KW - phosphoramidite KW - muraymycins KW - caprazamycins KW - nucleosides KW - uridine KW - cyclization KW - seven-membered rings KW - conjugated diyne KW - LAH reduction KW - diacetal KW - pent-1,2,3,4-tetraene intermediate KW - ligand KW - pyridine derivatives KW - allenic compounds KW - N-alkylation KW - copper KW - cyanide KW - network KW - guanidinium KW - unexpected iminium cation UR - https://www.unicat.be/uniCat?func=search&query=sysid:145174179 AB - The 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. ER -