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Sulphur Mechanisms
Displaying 31 mechanisms:
Sulphur- Corey-Winter reaction- diol to alkene
Sulphur- disulphides - reaction with sulphuryl chloride (SO2Cl2)
Sulphur- oxidation of sulphide to sulphoxide using NaIO4
Sulphur- Pummerer allylation
Sulphur- sulphide- hydrogenation with Raney Nickel
Sulphur- sulphides- formation of three membered rings from allyl sulphide and michael acceptor
Sulphur- sulphides- Pummerer reaction to form chlorosulphides
Sulphur- sulphides- reaction of allyl sulphide with electrophile
Sulphur- sulphides- reaction of beta-stabilised carbocation to form alkene
Sulphur- sulphides- Swern oxidation- alcohol to aldehyde
Sulphur- sulphones - stabilised anion as nucleophile
Sulphur- sulphones- Julia Olefin synthesis
Sulphur- sulphonium saltes- preparation from sulphide and MeI
Sulphur- sulphonium salts- intramolecular reaction with electrophile
Sulphur- sulphonium ylids- epoxides from sulphonium ylids
Sulphur- sulphoxide- ylid to cyclise (ninhydrin formation)
Sulphur- sulphoxide- ylid with sigmatropic rearrangement
Sulphur- sulphoxide- [2,3] sigma-tropic shift
Sulphur- sulphoxides- allylic sulphoxide rearrangement to sulphenate ester
Sulphur- sulphoxides- elimination
Sulphur- sulphoxides- Pummerer reaction
Sulphur- sulphoxides- Pummerer reaction- electrophilic aromatic substitution
Sulphur- sulponium ylids- (stabilised) conjugate addition
Sulphur- thioacetal- ketone fragmentation
Sulphur- thioacetals- formation from formaldehyde
Sulphur- thioacetals- hydrolysis using HgCl2
Sulphur- thioacetals- hydrolysis via methylation
Sulphur- thioacetals- hydrolysis via oxidation
Sulphur- thiol chlorides - electrophilic addition to alkene
Sulphur- thiol- acting as nucleophile
Sulphur- TsCl as nucloeophile- reaction with Zn