Results 221 to 230 of about 5,979 (235)
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ChemInform Abstract: Azomethine Ylide Generation via the Dipole Cascade.

ChemInform, 1992
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
D. C. Dean   +4 more
openaire   +3 more sources

Photooxygenation of aziridines and some potential azomethine ylides

The Journal of Organic Chemistry, 1979
Sensitized photooxygenations of a few bicyclic aziridines and some potential azomethine ylides have been investigated. The photooxygenation of 1-cyclohexyl-6-(cyclohexylimino)-1a-phenylindano(1,2-b)aziridine (7) gave a 51% yield of 2-cyclohexyl-3-hydroxy-3-phenylphthalimidine (12). The photooxygenation of endo-2,4,6-triphenyl-1,3-diazabicyclo(3.1.0)hex-
Manapurathu V. George, V. Bhat
openaire   +2 more sources

ChemInform Abstract: TRIMETHYLAMINE N‐OXIDE AS A PRECURSOR OF AZOMETHINE YLIDES

Chemischer Informationsdienst, 1983
AbstractDas aus dem N‐Oxid (I) mit Base generierte, nicht stabilisierte Azomethin‐Y1id (II) reagiert mit Olefinen (III) zu den N‐Methyl‐pyrrolidinen (IV).
G. Beugelmans, G. Roussi, G. Negron
openaire   +3 more sources

ChemInform Abstract: Intramolecular Cycloadditions with Azomethine Ylides for the Synthesis of Metacyclophanes.

ChemInform, 1986
Abstract3‐Hydroxy‐benzaldehyde (I) is converted to the cinnamic ester (II) which is then brominated, yielding (III).
I. Heinze   +4 more
openaire   +3 more sources

Tether-Mediated Stereocontrol in Intramolecular Azomethine Ylide Cycloadditions

The Journal of Organic Chemistry, 1994
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Stephen J. Klippenstein   +4 more
openaire   +3 more sources

Silver-Catalyzed Azomethine Ylide Cycloaddition [PDF]

open access: possibleSynfacts, 2013
Mark Lautens, David A. Petrone
openaire   +1 more source

1,3-Dipolar Cycloaddition of Azomethine Ylides [PDF]

open access: possibleSynfacts, 2006
Juan C. Carretero   +2 more
openaire   +1 more source

Enal-azomethine ylides: application in the synthesis of functionalized pyrroles

Organic & Biomolecular Chemistry
Novel enal-azomethine ylides derived from diazoenals and N-alkyl imines gave N-alkyl-3-formyl pyrroles. The new methodology was used in the short synthesis of biologically relevant pyrrolo[3,2-c]quinoline and pyrrolo[2,1-a]isoquinoline scaffolds.
Pratap Kumar Mandal   +2 more
openaire   +2 more sources

Development of amine functionalizations involving azomethine ylides

2015
Functionalization of amines is a very important research area in organic chemistry because functionalized amines are important building blocks in many biologically active compounds and pharmaceuticals. Outlined within this dissertation are our efforts toward the development of redox-neutral amine functionalizations involving azomethine ylides.
openaire   +2 more sources

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