amine ylide
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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
Staudinger reaction — The Staudinger reaction or Staudinger reduction is a chemical reaction in which the combination of an azide with a phosphine or phosphite produces an iminophosphorane intermediate [Staudinger, H.; Meyer, J. Helv. Chim. Acta 1919, 2 , 635.]… … Wikipedia
Aldehyde — An aldehyde. Formaldehyde, the simplest aldehyde … Wikipedia
Stevens rearrangement — The Stevens rearrangement in organic chemistry is an organic reaction converting quaternary ammonium salts and sulfonium salts to the corresponding amines or sulfides in presence of a strong base in a 1,2 rearrangement.The reactants can be… … Wikipedia
BASF AG — BASF SE Unternehmensform Societas Europaea ISIN … Deutsch Wikipedia
Badische Anilin- und Soda-Fabrik — BASF SE Unternehmensform Societas Europaea ISIN … Deutsch Wikipedia
Badische Anilin- und Sodafabrik — BASF SE Unternehmensform Societas Europaea ISIN … Deutsch Wikipedia
Badische Anilin und Soda Fabrik — BASF SE Unternehmensform Societas Europaea ISIN … Deutsch Wikipedia
Basf — SE Unternehmensform Societas Europaea ISIN … Deutsch Wikipedia
Imine — An imine is a functional group or chemical compound containing a carbon–nitrogen double bond [March Jerry; (1985). Advanced Organic Chemistry reactions, mechanisms and structure (3rd ed.). New York: John Wiley Sons, inc. ISBN 0 471 85472 7] . Due … Wikipedia
