perkin synthesis
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perkin reaction — noun also perkin synthesis ˈpərkə̇n Usage: usually capitalized P Etymology: after Sir William Henry Perkin died 1907 English chemist : a reaction for making an unsaturated aromatic acid (as cinnamic acid) by heating an aromatic aldehyde with an… … Useful english dictionary
Perkin, Sir William Henry — ▪ British chemist born March 12, 1838, London died July 14, 1907, Sudbury, near Harrow, Middlesex, Eng. British chemist who discovered aniline dyes. In 1853 Perkin entered the Royal College of Chemistry, London, where he studied under … Universalium
Perkin-Reaktion — Die Perkin Reaktion ist eine Namensreaktion und nach dem englischen Chemiker Sir William Henry Perkin benannt.[1][2] Die erste von ihm derartig synthetisierte Verbindung war Zimtsäure. Allgemein ist die Perkin Reaktion[3] eine Kondensation… … Deutsch Wikipedia
Perkin reaction — The Perkin reaction is an organic reaction developed by William Henry Perkin that can be used to make cinnamic acids by the aldol condensation of aromatic aldehydes and acid anhydrides in the presence of an alkali salt of the acid. [Perkin, W.… … Wikipedia
William Henry Perkin, Jr. — Infobox Scientist name = William Henry Perkin, Jr. image width = caption = birth date = 1860 birth place = Sudbury, England residence = England nationality = English death date = 1929 death place = field = work institution = Heriot Watt College,… … Wikipedia
Malonic ester synthesis — The malonic ester synthesis is a chemical reaction where diethyl malonate or another ester of malonic acid is alkylated at the carbon alpha (directly adjacent) to both carbonyl groups, and then converted to a substituted acetic acid.[1] The major … Wikipedia
Quinine total synthesis — In total synthesis, the Quinine total synthesis describes the efforts in synthesis of quinine over a 150 year period. The development of synthetic quinine is considered a milestone in organic chemistry although it has never been produced… … Wikipedia
Bartoli indole synthesis — The Bartoli indole synthesis (also called the Bartoli reaction) is the chemical reaction of ortho substituted nitroarenes with vinyl grignard reagents to form substituted indoles.Ref|Bartoli1989Ref|Bartoli1991Ref|Dobbs1999Ref|Dalpozzo2005The… … Wikipedia
Hemetsberger indole synthesis — The Hemetsberger indole synthesis (also called the Hemetsberger Knittel synthesis) is a chemical reaction that thermally decomposes a 3 aryl 2 azido propenoic ester into an indole 2 carboxylic ester. [Hemetsberger, H.; Knittel, D. Monatsh. Chem.… … Wikipedia
Erlenmeyer-Plöchl azlactone and amino acid synthesis — The Erlenmeyer Plochl azlactone and amino acid synthesis, named after Friedrich Gustav Carl Emil Erlenmeyer who partly discovered the reaction, is a series of chemical reactions which transform glycine to various other amino acids via an… … Wikipedia