- Phenyllithium
- Phe|nyl|li|thi|um; Syn.: Lithiumphenyl: H5C6—Li; im Allg. in org. Lsgm. angewandte lithiumorg. Verb. zur Einführung der Phenylgruppe.
Universal-Lexikon. 2012.
Universal-Lexikon. 2012.
Phenyllithium — Strukturformel Allgemeines Name Phenyllithium Andere Namen … Deutsch Wikipedia
phenyllithium — fenillitis statusas T sritis chemija formulė C₆H₅Li atitikmenys: angl. phenyllithium rus. фениллитий … Chemijos terminų aiškinamasis žodynas
Georg Wittig — (Georg Friedrich Karl Wittig; * 16. Juni 1897 in Berlin; † 26. August 1987 in Heidelberg) war ein deutscher Chemiker und Träger des Nobelpreises für Chemie 1979. Wittig fand einen Weg, die Carbonylgruppe einer organischen Verbindung in eine… … Deutsch Wikipedia
Danishefsky Taxol total synthesis — overview from raw material perspective The Danishefsky Taxol total synthesis in organic chemistry is an important third Taxol synthesis published by the group of Samuel Danishefsky in 1996 [1] two years after the first two efforts … Wikipedia
Organolithium reagent — An organolithium reagent is an organometallic compound with a direct bond between a carbon and a lithium atom. As the electropositive nature of lithium puts most of the charge density of the bond on the carbon atom, effectively creating a… … Wikipedia
Nicolaou Taxol total synthesis — overview from raw material perspective. The Nicolaou Taxol total synthesis, published by K. C. Nicolaou and his group in 1994 concerns the total synthesis of Taxol. This organic synthesis was included in Nicolaou s book, Classics in Total… … Wikipedia
Triphenylphosphine — Chembox new Name = Triphenylphosphine ImageFile = Triphenylphosphine structure.svg ImageName = Triphenylphosphine ImageFile1 = Triphenylphosphine ray 3D balls.png ImageName1 = Ball and stick model of the triphenylphosphine molecule IUPACName =… … Wikipedia
Wittig reaction — The Wittig reaction is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (often called a Wittig reagent) to give an alkene and triphenylphosphine oxide. [cite journal author = Georg Wittig, Ulrich Schöllkopf journal … Wikipedia
Ojima lactam — The Ojima lactam is an organic compound of some importance in the commercial production of Taxol. This lactam was first synthesized by Iwao Ojima [1]. The organic synthesis is an illustration of asymmetric synthesis via a chiral auxiliary. The… … Wikipedia
603-35-0 — Triphénylphosphine Triphénylphosphine Formule de la Triphénylphosphine Général Nom IUPAC … Wikipédia en Français