Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Syntheses of chiral nopinane-annelated pyridines of C2 and D2-symmetry : X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9H-fluoren-9-one, and 9,9’-bi-4,5-diazafluorenylidene. / Vasilyev, Eugene S.; Bagryanskaya, Irina Yu; Tkachev, Alexey V.
в: Mendeleev Communications, Том 27, № 2, 01.03.2017, стр. 128-130.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Syntheses of chiral nopinane-annelated pyridines of C2 and D2-symmetry
T2 - X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9H-fluoren-9-one, and 9,9’-bi-4,5-diazafluorenylidene
AU - Vasilyev, Eugene S.
AU - Bagryanskaya, Irina Yu
AU - Tkachev, Alexey V.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Reaction of (+)-pinocarvone oxime with 2-morpholinocyclopent-2-enone and FeCl3·6H2O affords chiral C2-symmetric fused derivative of 4,5-diazafluorene, whose oxidation with SeO2 gives nopinane-annelated derivatives of 4,5-diaza-9Hfluoren- 9-one (C2-symmetry) and of 9,9’-bi-4,5-diazafluorenylidene (D2-symmetry). Structures of the compounds synthesized were proved by X-ray crystallography.
AB - Reaction of (+)-pinocarvone oxime with 2-morpholinocyclopent-2-enone and FeCl3·6H2O affords chiral C2-symmetric fused derivative of 4,5-diazafluorene, whose oxidation with SeO2 gives nopinane-annelated derivatives of 4,5-diaza-9Hfluoren- 9-one (C2-symmetry) and of 9,9’-bi-4,5-diazafluorenylidene (D2-symmetry). Structures of the compounds synthesized were proved by X-ray crystallography.
KW - N-OXIDES
KW - ALLYLATION
KW - ALDEHYDES
KW - CHEMISTRY
KW - LIGANDS
KW - FECL3
UR - http://www.scopus.com/inward/record.url?scp=85016077690&partnerID=8YFLogxK
U2 - 10.1016/j.mencom.2017.03.006
DO - 10.1016/j.mencom.2017.03.006
M3 - Article
AN - SCOPUS:85016077690
VL - 27
SP - 128
EP - 130
JO - Mendeleev Communications
JF - Mendeleev Communications
SN - 0959-9436
IS - 2
ER -
ID: 10270220