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The Simmons–Smith reaction is an organic cheletropic reaction involving an organozinc carbenoid that reacts with an alkene (or alkyne) to form a cyclopropane. [ 1 ] [ 2 ] [ 3 ] It is named after Howard Ensign Simmons, Jr. and Ronald D. Smith .
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Amos B. Smith III was a fellow of the American Academy of Arts and Sciences and member of the ESPCI ParisTech Scientific Council. [ 4 ] In 2015, he was awarded the Royal Society of Chemistry 's Perkin Prize for Organic Chemistry "for his continued outstanding contributions to new organic reaction development, complex natural product total ...
Simmons–Smith reaction; Simonini reaction; Simonis chromone cyclization; Simons process; Skraup chinolin synthesis; Skraup reaction; Smiles rearrangement; S N Ar nucleophilic aromatic substitution; S N 1; S N 2; S N i; Solvolysis; Sommelet reaction; Sonn–Müller method; Sonogashira coupling; Sørensen formol titration; Staedel–Rugheimer ...
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Wilder-Smith earned three doctorates; his first PhD in 1941 in Physical Organic Chemistry from Reading University, England, his second in 1964 in Pharmacology from the University of Geneva, and his third from Eidgenössische Technische Hochschule (Swiss Federal Institute of Technology), Zurich.
Smith was appointed as an instructor of chemistry at the University of Minnesota – not yet a major research institution in chemistry at the time – following the completion of his PhD in 1920. By 1932 he had become full professor and the chief of the organic division of the department of chemistry, a position he would occupy for over 25 ...
Derek Bryce-Smith [2] (1926–2011) was an English chemist and professor of Organic Chemistry at the University of Reading from 1956 until his retirement in 1991. His work included organometallic chemistry , radical chemistry , photochemistry , environmental science , nutritional science and behavioural science .