LEADER 03496nam  2200817z- 450 
001 9910557494003321
005 20210501
035   $a(CKB)5400000000042891
035   $a(oapen)https://directory.doabooks.org/handle/20.500.12854/69095
035   $a(oapen)doab69095
035   $a(EXLCZ)995400000000042891
100   $a20202105d2020      |y         0
101 0 $aeng
135   $aurmn|---annan
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aNitro Compounds and Their Derivatives in Organic Synthesis
210   $aBasel, Switzerland$cMDPI - Multidisciplinary Digital Publishing Institute$d2020
215   $a1 online resource (120 p.)
311 08$a3-03943-148-X 
311 08$a3-03943-149-8 
330   $aNitro chemistry plays an important role in organic synthesis to construct new frameworks. This is due to the diverse properties of the nitro group. The strong electron-withdrawing ability of the nitro group reduces the electron density of the scaffold, facilitating reactions with nucleophiles or electron transfer. In addition, the ?-hydrogen of the nitro group is highly acidic, giving a stable anion, which facilitates reactions with both electrophilic and nucleophilic reagents. In addition, the nitro group also serves as a good leaving group, which facilitates transformation to a wide variety of functional groups. Despite the substantial contributions of many researchers, nitro chemistry is still an exciting and challenging research area. This book brings together recent original research and review articles contributed by an international team of leading experts and pioneers in organic synthesis using nitro groups. It is sure to provide useful information and promising insights for researchers.
606   $aResearch & information: general$2bicssc
610   $a1-methyl-2-quinolone
610   $a1,3-dicarbonyl compound
610   $a1,3-Dipole
610   $a1,4-dihydropyridines
610   $a8-nitro-5-RO-indolizines
610   $aanchimeric assistance
610   $aaromaticity
610   $aC-H functionalization
610   $aconjugate addition
610   $acycloaddition
610   $adearomatization
610   $aDiels-Alder reaction
610   $adihydrofuran
610   $adirect functionalization
610   $aelectron-withdrawing ability
610   $aelectrophilicity
610   $aenolate
610   $aepimerization
610   $ahexapyrrolohexaazacoronene
610   $aICT character
610   $aisoxazoline N-oxide
610   $aisoxazolo[4,3-b]pyridines
610   $anitration
610   $anitro
610   $anitro group
610   $anitroketone
610   $anitronate
610   $anitropyridines
610   $anucleophilic addition
610   $anucleophilic substitution
610   $anucleophilicity
610   $aorganic materials
610   $aoxazole-pyrrole ring transformation
610   $aPDE4 inhibitors
610   $aperylenediimide
610   $aPhenacylation of beta-nitropyridin-2-ones
610   $apyridone
610   $apyrrolidines
610   $aSNAr substitution
610   $atotal synthesis
615  7$aResearch & information: general
700   $aNishiwaki$b Nagatoshi$4edt$01294155
702   $aNishiwaki$b Nagatoshi$4oth
906   $aBOOK
912   $a9910557494003321
996   $aNitro Compounds and Their Derivatives in Organic Synthesis$93022942
997   $aUNINA