1,721,051 research outputs found
Mild reduction of N,N'-mercurio-bis-tosylhydrazones with sodium cyanoborohydride. Synthesis of N-aroyl-N'-tosylhydrazines and deoxigenation of aromatic Ketones
No full textThe deoxygenation of aromatic ketones through the reduction of N,N'-mercurio-bis-tosylhydrazones with sodium cyanoborohydride is reporte
Cyclization of o-(methylthio)-anilides with phosphonitrile dichloride: synthesis of 2-substituted benzothiazoles
No full textThe synthesis of 2-substituted benzothiazoles by cyclization of o-(methylthio)-anilides with phosphonitrile dichloride is reporte
Regiospecific C-alpha Deuteration of Alkyl Ketones: a New Efficient Indirect Procedure
No full textKetones were deuterated in a regiospecific way from 2-nitroketone
Pyridinium Chlorochromate: a Mild and Efficient Oxidant for 2-Nitroalcohols
No full textA mild procedure for the oxidation of nitroalkanols to the corresponding 2-nitroketones has been develope
Functionalized Nitroalkenes as Useful Reagents for Alkyl Anion Synthon
No full textA panorama of synthtic potentiality of nitroalkanes was reporte
Denitration of -Nitro Ketones by Treatment of their Tosylhydrazones with Lithium Aluminium Hydride: New Application of the Henry Reaction
No full textThe denitration of 2-nitroketones were reporte
Functionalized Nitroalkanes in Synthesis of 1,6-Dioxaspiro[4.5]decane Components of Paravespula vulgaris Pheromone
No full textSpiroketal were prepared from 2-nitrocycloalkanone
A Convenient Synthesis of (Z)-5-Undecen-2-one: A Pheromone from the Pedal Gland of the Bontebok (Damaliscus dorcas dorcas).
No full textNitroaldol condensation, oxidation and denitration are the steps of a new synthetic scheme for the preparation of (Z)-5-undecen-2-one in 54% overall yield
Azines from Erytro-1,2-diaryl-2-(2-tosylhydrazino)-ethan-1-ol Derivatives by Acid Treatment
No full textTosylhydrazines were the key precursors of azine
(Z)-1-Nitro-3-hexene as Reagent for (Z)-Hexen-1-yl Anion Synthon: Synthesis of (Z)-5-Octen-2-one and (Z)-1,Undecadien-5-one
No full text(Z)-1-Nitro-3-hexene is a versatile reagent corresponding to the (Z)-3-hexen-1-yl d1-synthon. Nitroaldol addition, oxidation and denitration are the steps of a new methodology to conveniently prepare the title compounds, which are popular intermediates in the synthesis of (Z)-jasmololone and (Z)-jasmone
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