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Clayden is for referencing the first edition (2001) of Organic Chemistry by Jonathan Clayden, Nick Greeves, Stuart Warren and Peter Wothers. It is based on the template {{ cite book }} . Parameters are:
He is perhaps best known as one of the authors of the best-selling undergraduate text Organic Chemistry (first edition 2000, [13] second edition 2012 [14]), which he wrote with his former students Jonathan Clayden and Nick Greeves, and fellow Cambridge lecturer Peter Wothers.
In 1992 he obtained his PhD [1] at the University of Cambridge working with Dr Stuart Warren on asymmetric synthesis using phosphine oxide chemistry. He then carried out a postdoc with Prof Marc Julia and in 1994 became a lecturer in organic chemistry at the University of Manchester where he became a reader in 2000 and a Professor of Organic ...
In organic chemistry, the Michael reaction or Michael 1,4 addition is a reaction between a Michael donor (an enolate or other nucleophile) and a Michael acceptor (usually an α,β-unsaturated carbonyl) to produce a Michael adduct by creating a carbon-carbon bond at the acceptor's β-carbon.
In organic chemistry, the oxymercuration reaction is an electrophilic addition reaction that transforms an alkene (R 2 C=CR 2) into a neutral alcohol. In oxymercuration, the alkene reacts with mercuric acetate (AcO−Hg−OAc) in aqueous solution to yield the addition of an acetoxymercury (−HgOAc) group and a hydroxy (−OH) group across the ...
Ethylene glycol protects a ketone (as an acetal) during an ester reduction, vs. unprotected reduction to a diol. A protecting group or protective group is introduced into a molecule by chemical modification of a functional group to obtain chemoselectivity in a subsequent chemical reaction.