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dc.contributor.editorD’Errico, Stefano
dc.date.accessioned2021-05-01T15:07:09Z
dc.date.available2021-05-01T15:07:09Z
dc.date.issued2021
dc.identifierONIX_20210501_9783036500041_78
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/68334
dc.description.abstractThe 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.
dc.languageEnglish
dc.subject.classificationbic Book Industry Communication::T Technology, engineering, agriculture::TB Technology: general issues::TBX History of engineering & technology
dc.subject.otheroxazole
dc.subject.otherfuran
dc.subject.otherRORC reaction
dc.subject.other(E,Z)-isomerization
dc.subject.othernitration
dc.subject.otherazaheterocycles
dc.subject.otherN–C bond cleavage
dc.subject.otherpyridine-imidazolium
dc.subject.otherribose
dc.subject.otherpsicose
dc.subject.otherketose
dc.subject.otherrare sugar
dc.subject.otherhydroxy methylation
dc.subject.otherAICAR
dc.subject.otheracadesine
dc.subject.otherphosphorylation
dc.subject.otherfluorination
dc.subject.otherfluorinated nucleosides
dc.subject.othernucleoside analogues
dc.subject.othermodified nucleosides
dc.subject.otherchlorinated nucleosides
dc.subject.otherAMPK
dc.subject.otherorganic synthesis
dc.subject.otherbidentate directing groups
dc.subject.otherbenzamides
dc.subject.otherchelation assistance
dc.subject.otherbis-chelates
dc.subject.otherC–H bond functionalization
dc.subject.otherX-ray structure determination
dc.subject.otherN′-acetylhydrazide
dc.subject.other3-acetyl-2,3-dihydro-1,3,4-oxadiazole
dc.subject.other1H-pyrazolo[3,4-b]pyridine
dc.subject.otherheterocycle
dc.subject.otheroxetane
dc.subject.otherepoxide
dc.subject.otherrearrangement
dc.subject.othercarbohydrate
dc.subject.otherC-glycosylation
dc.subject.otherspiro-oxetane
dc.subject.otherester group migration
dc.subject.otherglycosyl sulfoxide
dc.subject.otheruronate
dc.subject.otherthioglycoside oxidation
dc.subject.othermannose
dc.subject.other8-Fluoro-2′-deoxyguanosine
dc.subject.other19F NMR spectroscopy
dc.subject.othersolid phase synthesis
dc.subject.otherphosphoramidite
dc.subject.othermuraymycins
dc.subject.othercaprazamycins
dc.subject.othernucleosides
dc.subject.otheruridine
dc.subject.othercyclization
dc.subject.otherseven-membered rings
dc.subject.otherconjugated diyne
dc.subject.otherLAH reduction
dc.subject.otherdiacetal
dc.subject.otherpent-1,2,3,4-tetraene intermediate
dc.subject.otherligand
dc.subject.otherpyridine derivatives
dc.subject.otherallenic compounds
dc.subject.otherN-alkylation
dc.subject.othercopper
dc.subject.othercyanide
dc.subject.othernetwork
dc.subject.otherguanidinium
dc.subject.otherunexpected iminium cation
dc.subject.othern/a
dc.titleMolecules from Side Reactions
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-0005-8
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036500041
oapen.relation.isbn9783036500058
oapen.pages100
oapen.place.publicationBasel, Switzerland


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