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Artikel 99981 C 1 -Substituted N - tert -butoxycarbonyl-5- syn - tert -butyldimethylsilyloxymethyl-2-azabicyclo (2.1.1) hexanes as conformationally constrained β-amino acid precursors
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 6: 319-328. 10 S.
Online Ressource
Artikel 99982 Synthesis of spiro (pyrazole-4,8′-pyrazolo (3,4- f) quinolin)-5 (1 H)-ones by the reaction of aldehydes with 1 H -indazol-6-amine and 1 H -pyrazol-5 (4 H)-one
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 5: 307-310. 4 S.
Online Ressource
Artikel 99983 Convenient synthesis of the functionalized 1′,3′-dihydrospiro (cyclopentane-1,2′-inden)-2-enes via a three-component reaction
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 5: 301-306. 6 S.
Online Ressource
Artikel 99984 Halogenoheterocyclization of 2-(allylthio) quinolin-3-carbaldehyde and 2-(propargylthio) quinolin-3-carbaldehyde
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 5: 295-299. 5 S.
Online Ressource
Artikel 99985 Novel 5,6,7,8-tetrahydroimidazo (2′,1′:2,3) thiazolo (5,4- c) pyridine derivatives
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 5: 291-294. 4 S.
Online Ressource
Artikel 99986 Polymeric (anion-π) n interactions in crystals of 2-(2,4,6-trioxo-(1,3,5) triazinan-1-yl) ethylammonium iodide
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 5: 281-285. 5 S.
Online Ressource
Artikel 99987 Microwave-assisted one-pot synthesis and antimicrobial evaluation of 2-(1-phenyl-3-(2-thienyl)-1 H -pyrazol-4-yl) chroman-4-one derivatives
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 5: 259-264. 6 S.
Online Ressource
Artikel 99988 Design, synthesis and cytotoxicity evaluation of novel (E)-3-(3-aryl-1-phenyl-1 H -pyrazol-4-yl)-1-(pyridin-3-yl) prop-2-en-1-ones as anticancer agents
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 4: 221-225. 5 S.
Online Ressource
Artikel 99989 FENS Forum 2018 in Berlin
Enthalten in e-Neuroforum Bd. 22, 2016, Nr. 4: 109-109. 1 S.
Online Ressource
Artikel 99990 A direct synthetic route to fused tricyclic quinolones from 2,3-diaminoquinolin-4 (1 H) one
Enthalten in Heterocyclic communications Bd. 22, 2016, Nr. 3: 169-173. 5 S.
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