carbenoid
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Carbenoid — In chemistry a carbenoid is a reactive intermediate that shares reaction characteristics with a carbene [ Organic Chemistry john McMurry Brooks /Cole Publishing Company 1988 ISBN 0 534 07968 7] . In the Simmons Smith reaction the carbenoid… … Wikipedia
carbenoid — karbenoidas statusas T sritis chemija apibrėžtis Lengvai virstantis karbenu junginys. atitikmenys: angl. carbenoid rus. карбеноид … Chemijos terminų aiškinamasis žodynas
Carbenoid — Car|be|no|id [↑ Carben u. ↑ oid], das; s, e: eine carbenartig reagierende oder ein Carben freisetzende Verbindung … Universal-Lexikon
Cyclopropane — Cyclopropane[1] … Wikipedia
Johnson–Corey–Chaykovsky reaction — The Johnson–Corey–Chaykovsky reaction (sometimes referred to as the Corey–Chaykovsky reaction or CCR) is a chemical reaction used in organic chemistry for the synthesis of epoxides, aziridines, and cyclopropanes. It was discovered in 1961 by A.… … Wikipedia
Transition metal carbene complex — A transition metal carbene complex is a organometallic compound featuring a divalent organic ligand. The divalent organic ligand coordinated to the metal center is called a carbene. Carbene complexes for almost all transition metals have been… … Wikipedia
Organotitanium compound — Organotitanium compounds Organotitanium compounds in organometallic chemistry contain carbon to titanium chemical bonds. Organotitanium chemistry is the science of organotitanium compounds describing their physical properties, synthesis and… … Wikipedia
Zinc — This article is about the metallic element. For other uses, see Zinc (disambiguation). copper ← zinc → gallium ↑ Zn ↓ Cd … Wikipedia
Nitrous acid — Preferred IUPAC name Nitrous acid … Wikipedia
Asymmetric synthesis — Asymmetric synthesis, also called chiral synthesis, enantioselective synthesis or stereoselective synthesis, is organic synthesis which introduces one or more new and desired elements of chirality. [GoldBookRef|title=asymmetric synthesis| file =… … Wikipedia
